摘要
背景/目的:本回顾性研究在腭裂患者中考察了以下问题:犬齿萌出状态是否与侧切牙状态相关;裂隙宽度是否因侧别、年龄或性别而异;鼻腭管及鼻中隔位置是否与裂隙侧别相关。方法:回顾了33例患者的CBCT检查资料,包括7例单侧右侧、14例单侧左侧和12例双侧病例的小型亚组。侧切牙与犬齿状态采用Fisher精确检验进行比较;裂隙宽度按侧别、年龄和性别采用Kruskal–Wallis检验、Spearman检验和Mann–Whitney U检验进行比较;鼻腭管及鼻中隔位置与侧别的关系采用Fisher–Freeman–Halton检验,并排除6例最年幼患者后重复比较。结果:犬齿萌出状态与侧切牙状态无关(右侧p = 1.000;左侧p = 0.733)。存在的侧切牙中13.2%发生牙根吸收,45.5%的患者至少缺失一颗侧切牙(年龄、性别和侧别的所有p > 0.14)。犬齿萌出状态与年龄相关(未萌出犬齿者更年轻,10.8岁 vs. 15.1岁;p = 0.005)。裂隙宽度不因侧别、年龄或性别而异(所有p > 0.14;ICC 0.974)。鼻腭管及鼻中隔位置与侧别显著相关(p = 0.002,p = 0.001):单侧病例中87.5%的鼻腭管偏向裂隙对侧,90.5%的鼻中隔偏向裂隙侧;排除最年幼患者后结果不变。这两个变量的检查者内信度几乎完美(Cohen's κ = 0.86–0.88)。结论:牙槽部所见与裂隙侧别无显著关联,除预期的年龄-萌出关系外,且鉴于样本量有限,应视为不确定结论。相比之下,鼻腭管及鼻中隔位置与侧别呈显著且相互对应的相关性,符合腭裂反映区域性颅面发育紊乱而非孤立性牙槽缺损的认识,在更大队列证实之前对术前规划具有参考意义。
关键词:锥形束计算机断层扫描,腭裂,唇裂,鼻腭管,鼻中隔,牙槽部异常,牙槽裂,裂隙侧别
1. 引言
口面裂,包括唇裂、腭裂及唇腭裂复合型,是最常见的先天性颅面畸形之一。近期一项系统综述和荟萃分析将全球患病率定为每1000例活产0.45例,各区域单项研究的数据通常约在每500至700例活产1例之间[1]。Mossey[2]强调了国际多中心出生缺陷登记系统对于在遗传和环境背景不同的人群中建立一致流行病学关联的价值。来自相关国际典型口裂围产期数据库(IPDTOC)的汇总数据显示,唇裂伴或不伴腭裂的出生患病率在不同人群间存在六倍差异,孤立性腭裂存在三倍差异[3],而针对阿拉伯人群的区域性综述报告口面裂平均患病率约为每1000例活产1.1例,腭裂在该区域多个国家被确定为优势亚型[4]。除面部和鼻部畸形本身外,口面裂还持续伴随裂隙区域一系列牙槽部紊乱,包括牙齿发育不全、牙齿畸形或移位、萌出顺序改变及牙槽骨结构异常,这些共同使长期正畸和外科康复复杂化[5]。
牙槽裂是上颌牙槽突的骨性缺损,该区域正常情况下容纳侧切牙和犬齿的牙根,存在于大多数唇裂和/或腭裂患者中[1]。由于该缺损可干扰邻近牙列的牙槽部生长、牙齿萌出和牙周支持,对其尺寸进行准确的三维表征对于外科和正畸规划至关重要。二维X线片低估颊舌向骨丧失,且无法可靠描绘缺损的真实结构,这推动了CBCT作为裂隙评估首选影像学模式的转变。评估不同CBCT定量牙槽裂缺损方法的比较研究已证实,三维体积评估比任何单平面方法更准确[6],一项比较计算机模拟与排水法在CBCT上进行术前裂隙体积测量的研究也得出了相同结论[7]。
唇裂侧别本身似乎影响移植结局和残余缺损体积:一项针对采用分期两步法植骨治疗的双侧牙槽突裂的三维体积测量研究发现,首先移植的一侧获得的骨充填量(47%)显著大于其次移植的一侧(33%),且对侧尚未移植的裂隙体积在第一次手术后无实质性变化——这证明双侧裂隙表现为两个至少部分独立的缺损,而非单一对称实体,这对如何将唇裂侧别作为变量进行分析具有直接意义[8]。校正矢状面重建——重新定向为垂直于牙弓而非真正的解剖平面——已成为这些方案中轴位视图的标准辅助手段,因为它能够沿邻近牙根长轴无遮挡地显示裂隙边缘[9]。
上颌侧切牙是唇腭裂患者中最常受发育障碍影响的牙齿,因为其牙胚直接位于或邻近裂隙边缘。López-Giménez等[10]使用牙齿缺失编码报告,在一个西班牙队列中,单侧和双侧唇腭裂的缺失患病率均约为51%,其中侧切牙是最常缺失的牙齿,尤其是在裂隙象限内。Bartzela等[11]同样发现在一个完全性单侧唇腭裂患者的荷兰队列中,近半数受试者存在牙齿缺失,约五分之二的患者裂隙侧侧切牙缺失。一项对唇裂人群中牙齿异常的更广泛综述证实,上颌侧切牙缺失是跨唇裂严重程度和种族最为一致的发现,此外还有多生牙、小牙症和牛牙症[12]。
当存在的侧切牙位置靠近移位或正在萌出的尖牙时,可能发生牙根吸收——这是正畸文献中已有充分描述的现象,Alqerban等[13]综合了由邻近阻生尖牙引起的侧切牙牙根吸收的危险因素,包括尖牙倾斜度、影像学重叠程度和唇腭侧位置。一项更近期基于CBCT的大型回顾性研究纳入305例单侧上颌阻生尖牙患者,证实较薄的唇侧牙槽骨板和更向唇侧倾斜的侧切牙牙根与更大程度的吸收独立相关,且吸收患病率因尖牙的唇腭侧位置而异[14]。具体在唇裂人群中,骨缺损、常旋转或移位的侧切牙以及非典型尖牙萌出路径共存,形成了独特的解剖背景,而这一吸收过程尚未在该背景下得到系统记录——本研究通过将侧切牙状态分类为存在、缺失或牙根吸收来弥补这一空白。
唇裂患者的上颌尖牙萌出路径常因邻近骨缺损、侧切牙的存在与否以及继发性牙槽突植骨相对于牙根发育的时机而发生改变。Oberoi等[9]在对植骨牙槽突裂中尖牙萌出路径的三维评估中发现,侧切牙先天性缺失与尖牙牙根发育完成或萌出失败之间无显著关联,而其他研究者报告了侧切牙缺失与尖牙阻生率增加之间的关联,尽管证据确定性较低。Grisar等[15]的一项系统综述发现,阻生上颌尖牙的初始三维位置——倾斜度、垂直位移和近中区位置——对近1600颗阻生尖牙治疗结局的预测能力强于仅凭萌出状态。对于解读混合牙列或青少年早期唇裂样本中的萌出状态而言,重要的是,影像检查时未萌出的尖牙并不一定表明病理性阻生:上颌尖牙的生理性萌出通常发生在7至11岁之间,年轻患者中仍沿正常路径下降的尖牙应归类为发育中而非阻生[5]。这一区分支持将本研究中的尖牙状态界定为描述性的、基于患病率的变量——已萌出或未萌出——而非阻生的临床诊断。
鼻腭(切牙)管是连接鼻腔底与硬腭前部的中线结构,位于上颌中切牙后方。在非唇腭裂人群中,CBCT形态测量研究描述了该管在形状、长度和直径上的显著变异,男性通常表现为比女性更长、更宽的管[16],并且已有文献记录了与牙槽骨吸收及种植规划相关的管形态学变化[17]。一项直接比较唇腭裂与非唇腭裂患者鼻腭管的研究,使用在冠状面、矢状面和轴面重建上评估的CBCT检查,发现漏斗形、香蕉形和针形管在唇腭裂患者中显著更常见,同时与非唇腭裂对照组相比,鼻腭孔和管直径显著更大,但管的总体长度显著更短[18]。另一项专门评估裂隙体积及邻近解剖结构的CBCT调查发现,在71%的双侧唇腭裂病例中切牙孔不可见,显著低于单侧唇腭裂的发生率,表明裂隙缺损本身在更严重的表现形式中可能直接累及或 obliterate 管的口腔开口[19]。这些发现共同支持了这一前提:作为牙槽突裂基础的胚胎融合中断也重塑了这一邻近的中线管,强化了在规划植骨或种植修复时表征该管与裂隙边缘邻近关系的临床相关性。
鼻中隔偏曲是唇腭裂相关的最一致的继发畸形之一,既源于原发胚胎缺陷,也源于手术修复前跨越裂侧唇和牙槽突的不平衡肌肉牵拉。一项使用直接视觉评分的早期研究表明,鼻中隔偏曲在唇腭裂个体中显著比非唇腭裂对照组更常见,鼻软骨尖和鼻前棘均倾向于偏向非裂侧[20]。使用CBCT,一项被广泛引用的耳鼻咽喉科研究调查了腭裂和/或牙槽突裂患者的鼻中隔偏曲,发现偏曲程度与裂隙严重程度显著相关[21],而随后的一项三维CBCT分析量化了鼻前棘、鼻后棘及其中点处的鼻中隔偏曲角度和线性位移,发现单侧唇腭裂患者的偏曲显著大于骨性III类非唇腭裂对照组[22]。上述结合裂隙体积与邻近结构的CBCT研究同样发现,在87%的单侧病例中鼻中隔向裂隙或植骨侧弯曲,并且还发现裂侧下鼻甲显著小于非裂侧[19]。
总体而言,这些文献确立了与本研究中每个变量——牙槽突裂形态测量、侧切牙状态、尖牙萌出模式、鼻腭管形态和鼻中隔偏曲——均为唇腭裂表型中已被独立研究的公认特征。然而,很少有(如果有的话)已发表研究在单一队列中结合所有这些参数,使用包含轴面和校正冠状面的标准化CBCT方案,更少有研究在同一批患者中考察侧切牙状态(存在、缺失或牙根吸收)如何与尖牙萌出模式、裂隙尺寸以及两个邻近中线结构——鼻腭管和鼻中隔——的位置共同相关。这种整合的、患病率与相关性相结合的方法——而非进一步的单一结构分析——是本研究的特定贡献。
这一范围也源于成像方式:CBCT能很好地捕捉矿化的骨性结构,但不能可靠显示软组织唇。因此,唇腭裂患者的基于CBCT的骨评估方案特别集中于牙槽骨和腭部骨骼[23,24]。出于这一原因,我们将本研究范围限定为腭裂——CBCT实际可视化的骨性成分——而非作为软硬组织联合诊断的唇腭裂。
1.1. 目的
本研究的一般目的是使用锥形束计算机断层扫描评估腭裂患者的牙槽骨及解剖特征及其与裂隙侧别的统计学关系。具体目的如下:
确定腭裂患者上颌尖牙萌出状态(已萌出 vs. 未萌出)是否与侧切牙状态(存在 vs. 缺失)存在统计学关联,使用Fisher精确检验进行检验。
测量二维牙槽突裂宽度——轴面上的近远中宽度和校正冠状面上的颊腭深度——并比较单侧与双侧唇腭裂病例之间的裂隙宽度。
确定鼻腭管位置和鼻中隔偏曲的患病率,并检验其与裂隙侧别(单侧右侧、单侧左侧或双侧)的统计学相关性。
1.2. 假设
原假设(H0):上颌尖牙萌出状态与侧切牙状态无显著关联;单侧与双侧腭裂病例的牙槽突裂宽度无显著差异;鼻腭管位置及鼻中隔偏斜与腭裂侧别无显著相关性。
备择假设(H1):上颌尖牙萌出状态与侧切牙状态显著相关,即侧切牙缺失与尖牙未萌出率不同相关;单侧与双侧腭裂病例的牙槽突裂宽度存在显著差异;鼻腭管位置及鼻中隔偏斜与腭裂侧别显著相关。
2. 材料与方法
2.1. 研究设计与场所
本回顾性横断面研究使用存档于沙特阿拉伯吉达阿卜杜勒阿齐兹国王大学牙科医院(KAUDH)口腔放射科的CBCT检查资料。本报告遵循横断面研究的STROBE(加强流行病学观察性研究报告)指南;完整的STROBE清单作为补充文件File S1提供。
2.2. 病例选择
通过回顾性检索口腔放射科档案,筛选2024年8月至2026年6月期间作为常规多学科腭裂诊疗的一部分接受CBCT成像的腭裂患者病例。
纳入标准为:临床诊断为唇裂和/或腭裂;存有为常规多学科腭裂诊疗采集的CBCT检查资料;图像质量和视野足以显示牙槽突裂及鼻腭管和鼻中隔。三种情况导致排除:CBCT拍摄前牙槽突裂已手术关闭;初疑为腭裂但复核为孤立性中线间隙;以及临床和影像学复核未确认腭裂的任何病例。由于CBCT扫描仅能检测骨结构,我们仅研究腭裂,未对唇裂进行评估。
最初有36例CBCT检查符合检索标准。分析前排除3例:1例因CBCT采集前牙槽突裂已手术关闭,1例因初判为腭裂的发现实为孤立性中线间隙,1例因临床和影像学记录复核确认患者无腭裂。其余33例检查构成合格的分析队列(图1)。我们未进行先验样本量计算。本研究仅纳入研究期间档案中所有符合条件的检查,符合本分析的探索性、回顾性性质。第4节讨论了最终样本量及其对较小亚组留下的有限检验效能。
[图:病例选择流程图:已识别的检查、排除原因及最终合格的分析队列。]

合格队列可获得以下变量:性别、成像时年龄、腭裂侧别、上颌侧切牙状态、上颌尖牙状态、鼻腭管位置及鼻中隔偏斜。
由于年轻患者牙齿发育可能不完全,对牙根吸收和萌出状态的判读尤其谨慎。6例患者(18.2%)在成像时为7~8岁。这些患者保留在主分析中,但依赖牙根发育或生理性萌出时序的结果在判读时考虑了发育阶段。
当同一患者有多次合格CBCT检查时,选择用于分析的是能充分显示研究所需结构的最早合格治疗前检查。当同一治疗节点前后有多次检查时,优先选择牙齿发育更完整且图像质量合格的检查。
2.3. CBCT采集与图像评估
CBCT检查使用研究期间口腔放射科现有设备采集。大多数检查使用KaVo 3D eXam® CBCT设备(KaVo Dental GmbH,Biberach,德国)获取,一部分使用i-CAT®设备(Imaging Sciences International/KaVo Kerr,Hatfield,PA,美国)采集。
使用KaVo 3D eXam设备采集的检查,标准曝光参数为90 kV、6.3 mA、曝光时间8.7 s,剂量面积乘积为509 mGy/cm²。由于本研究使用回顾性临床档案,各检查的视野不统一。然而,所有纳入检查均涵盖双侧上颌骨,可评估裂侧和对侧区域。大多数检查使用0.3 mm各向同性体素大小。
CBCT数据集使用OnDemand3D成像软件(Cybermed Inc.,首尔,韩国)审阅。图像通过轴位、矢状位和冠状位的多平面重建(MPR)进行评估(图2)。当有助于评估牙齿存在、萌出状态和整体牙体解剖时,也审阅全景重建图像。
[图:用于图像评估的代表性CBCT重建、多平面视图及全景重建。(A) Th]

患者年龄和性别取自临床影像记录,并与存档的患者信息进行交叉核对。
2.4. 测量方案与参考平面
所有线性测量均采用标准化的图像定向方案。
对于矢状面评估,水平参考线平行于硬腭底面定向。对于轴面和冠状面评估,解剖中线以鼻中隔中点确定。采用解剖中线而非牙中线,是因为裂隙相关的前牙列移位可能改变牙中线的位置。由于同一鼻中隔参考也用于鼻中隔位置的分类(第2.5节),鼻腭管——一个独立结构——是参照该中线进行评估的,不存在循环论证问题,但在本回顾性数据集中,鼻中隔位置无法参照完全独立的骨骼标志进行评估;这一点已作为局限性明确说明(第4节)。
评估了两项线性裂隙测量指标:
轴面近远中向裂隙宽度:在轴面CBCT重建图像上,于牙槽突冠三分之一处、约牙槽嵴根方1 mm处测量。该测量代表跨牙槽裂隙、位于中切牙与毗邻缺损的侧切牙或尖牙之间的近远中距离(图3)。
[图:展示单侧(右侧)裂隙病例中裂隙宽度测量的代表性CBCT图像。(A) Axial C]

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校正冠状面颊腭向裂隙深度:在腭中平面水平的校正冠状面重建图像上测量。校正冠状面垂直于牙弓定向,并定位为通过相关毗邻牙齿结构。当侧切牙存在时,于侧切牙根方远中获取测量值;当侧切牙缺失时,则相对于尖牙获取测量值。使用校正冠状面重建是为了获得垂直于相关牙齿解剖结构的平面,并尽量减少裂隙三维方向所致的测量失真。
在双侧裂隙病例中,若两个裂隙间隙形成连续性缺损,则参照解剖中线评估该缺损,并在解剖结构允许进行侧别特异性评估时,分别记录右侧和左侧部分的测量值。
可获得45个裂隙侧观察的轴面裂隙宽度测量值。可获得44个裂隙侧观察的校正冠状面颊腭向深度测量值。“裂隙侧观察”指一个可测量的裂隙边缘;单侧患者贡献一个此类观察,双侧患者最多可贡献两个,因此这些计数超过33例患者的队列。
2.5. 变量与分类
每例患者记录以下变量:
性别;
CBCT成像时的年龄;
裂隙侧别(单侧右侧、单侧左侧或双侧);
#12和#22牙上颌侧切牙状态;
#13和#23牙上颌尖牙状态;
鼻腭管位置;以及
鼻中隔偏曲。
上颌侧切牙状态
每颗上颌侧切牙按如下分类:
存在,无根尖牙根吸收;
存在,伴根尖牙根吸收;或
成像时缺失。
在统计分析中,侧切牙状态进一步二分为存在或缺失。在存在的侧切牙中,牙根吸收作为单独的二分类变量进行分析。
“缺失”一词指CBCT检查时未能识别出恒侧切牙,并不一定确立先天性缺牙,尤其是在年轻患者中。在无法可靠区分滞留乳侧切牙与发育中的恒牙继承牙的情况下,该放射学时间点将恒侧切牙记录为缺失,而非解释为确诊的先天性缺牙(图4)。
[图:展示裂隙毗邻上颌侧切牙状态的代表性CBCT图像。(A) Correc]

上颌尖牙状态
每颗上颌尖牙分类为已萌出或未萌出。
未萌出类别包括CBCT检查时仍位于骨内的尖牙。有意使用该分类而非“阻生”,因为单次CBCT检查无法可靠区分病理性阻生与正常发育性未萌出,尤其是在年轻患者中。
鼻腭管位置
鼻腭管根据其相对于解剖中线的位置分类如下:
偏向右侧;
居中/中线;或
偏向左侧。
当无法可靠定位该管时,以解剖中线为参考,将该管分类为居中,而非赋予不确定的方向性偏斜。
鼻中隔偏曲
鼻中隔位置分类如下:
偏向右侧;
偏向左侧;或
无明显偏曲。
由于上文(第2.4节)所采用的解剖学中线本身即来源于鼻中隔,因此该变量描述的是鼻中隔相对于本研究自身参考线的走行,而非经完全独立骨骼轴线验证的偏移;此点在第四节中作为局限性加以讨论。
2.6. 检查者可靠性与数据质量控制
所有图像评估均由同一名口腔颌面放射科医师(H.S.)完成。
为评估检查者自身可靠性,在间隔足够长的时间以尽量减少对初次测量记忆后,对一部分检查进行了重新评估。重复评估包括轴位裂隙宽度和校正冠状位颊腭深度的测量。每个测量类别的重复病例数为10至13例。
可靠性采用双向混合效应组内相关系数评估绝对一致性和单次测量[ICC(A,1)]。同时计算了第一次与第二次测量之间的平均有符号差值及95%一致性界限。
所有测量结果随后在统计分析前均与原始CBCT检查和源数据进行核对。任何明显的数据录入差异均通过返回原始CBCT数据集并记录经核实的测量值来解决。
对于鼻腭管位置和鼻中隔偏移——本研究主要显著发现所依据的两个分类变量——检查者自身可靠性还通过对全部33例进行盲法重读加以评估,一致性采用Cohen's kappa量化:鼻腭管位置κ = 0.86,鼻中隔偏移κ = 0.88(两者均为几乎完全一致;见第3.3.1节)。在本回顾性数据集中,犬齿或侧切牙状态的重复分类判读数据不可获得。
2.7. 统计分析
犬齿和侧切牙状态属于特定牙齿和特定侧别,因此我们在牙-侧别水平分析这两个变量。相比之下,裂隙侧别、裂隙宽度、鼻腭管位置和鼻中隔偏移是患者整体的属性而非单颗牙齿的属性,因此我们在患者水平进行分析。我们在以下所有分析中始终保持这一区分。对所有变量计算了描述性统计量。分类变量采用频数和百分比进行汇总。连续变量采用均值、标准差、中位数和范围进行汇总。
对于目标1,同侧侧切牙状态(存在 vs. 缺失)与犬齿萌出状态(已萌出 vs. 未萌出)之间的关联分别在右侧(#12/#13)和左侧(#22/#23)采用Fisher精确检验进行评估。由于同一患者的左右牙-侧别观察值在统计学上并非独立,汇总的双侧牙-侧别数据仅作描述性呈现,未再进行额外的推断性Fisher精确检验。
在患者水平,采用卡方检验评估裂隙侧别与至少一颗侧切牙缺失的存在之间的关系,以及裂隙侧别与至少一颗犬齿未萌出的存在之间的关系。采用Fisher精确检验评估性别与至少一颗侧切牙缺失的存在之间的关系。
采用Mann–Whitney U检验比较有和无至少一颗侧切牙缺失的患者之间、有和无牙根吸收的患者之间、以及有至少一颗犬齿未萌出与两颗犬齿均已萌出的患者之间的年龄。
特定裂隙累及侧与牙齿水平发现之间的关系采用描述性方法评估,并在适当情况下采用Fisher精确检验,因为双侧病例贡献了来自两侧的观察值,因此不代表独立的患者水平观察值。
对于目标2,轴位裂隙宽度和校正冠状位颊腭深度按侧别进行汇总。对于按裂隙侧别的比较,对每位患者可用裂隙侧的轴位宽度取平均值,所得患者水平值在单侧左侧、单侧右侧和双侧裂隙组之间采用Kruskal–Wallis检验进行比较。此外还采用Mann–Whitney U检验进行了简化的单侧与双侧比较。患者年龄与平均轴位裂隙宽度之间的关系采用Spearman秩相关系数进行评估。
对于目标3,鼻腭管位置与裂隙侧别之间以及鼻中隔偏移与裂隙侧别之间的关联采用Fisher–Freeman–Halton精确检验进行评估,因为3×3列联表中单元格计数稀疏。同时计算了Pearson卡方统计量作为参考统计量。在单侧病例中,鼻腭管位置和鼻中隔偏移相对于裂隙侧的方向以同侧偏移或对侧偏移进行描述性汇总。
双侧p值 < 0.05视为具有统计学显著性。由于多项分析为探索性且本研究基于相对较小的回顾性队列,p值的解读结合了效应方向、样本量和测量数据可获得性的背景,而非作为无关联的确定性证据。
统计分析采用Python 3.11版本及pandas和SciPy库完成。
在撰写本手稿期间,作者使用了基于人工智能的写作与分析助手 Claude Sonnet 5(Anthropic)进行文献检索支持、统计交叉核对和语言编辑辅助。作者已审阅并编辑了输出内容,并对本出版物的内容承担全部责任。
3. 结果
3.1. 样本特征
在最初确定的36例CBCT检查中,排除了3例(第2.2节详述了纳入/排除标准及原因);最终分析队列包括33例患者(图1)。
该队列包括17例女性(51.5%)和16例男性(48.5%)。成像时的平均年龄为12.5 ± 4.1岁,中位数为12.0岁,范围为7–23岁。6例患者(18.2%)在成像时为7–8岁。
单侧左侧唇裂是最常见的表现(n = 14,42.4%),其次是双侧唇裂(n = 12,36.4%)和单侧右侧唇裂(n = 7,21.2%)(表1)。
Table 1. Sample characteristics of the study cohort ( n = 33).
| Characteristic | n | % |
|---|---|---|
| Female | 17 | 51.5 |
| Male | 16 | 48.5 |
| Age 7–8 years | 6 | 18.2 |
| Age ≥9 years | 27 | 81.8 |
| Unilateral left cleft | 14 | 42.4 |
| Bilateral cleft | 12 | 36.4 |
| Unilateral right cleft | 7 | 21.2 |
3.2. 目标1:上颌侧切牙和尖牙状态
对于#12牙,33例患者中有18例(54.5%)存在无根尖牙根吸收的侧切牙,2例(6.1%)存在根尖牙根吸收,13例(39.4%)在成像时无可识别的恒侧切牙。
对于#22牙,15例患者(45.5%)存在无根尖牙根吸收的侧切牙,3例(9.1%)存在根尖牙根吸收,15例(45.5%)无可识别的恒侧切牙。
当对两侧进行描述性考虑时,66个牙-侧观察中有28个(42.4%)被分类为缺失,38个(57.6%)为存在(表2)。
Table 2. Maxillary lateral incisor status by tooth ( n = 33).
| Status | Tooth #12, n (%) | Tooth #22, n (%) |
|---|---|---|
| Present without root resorption | 18 (54.5) | 15 (45.5) |
| Present with apical root resorption | 2 (6.1) | 3 (9.1) |
| Absent | 13 (39.4) | 15 (45.5) |
上颌尖牙状态被分类为已萌出或未萌出。对于#13牙,20例患者(60.6%)存在未萌出尖牙,13例(39.4%)存在已萌出尖牙。对于#23牙,19例患者(57.6%)存在未萌出尖牙,14例(42.4%)存在已萌出尖牙。该队列中未发现先天性上颌尖牙缺失(表3)。
Table 3. Maxillary canine eruption status by tooth ( n = 33).
| Status | Tooth #13, n (%) | Tooth #23, n (%) |
|---|---|---|
| Unerupted | 20 (60.6) | 19 (57.6) |
| Erupted | 13 (39.4) | 14 (42.4) |
在右侧,#12牙缺失的13例中有8例(61.5%)存在未萌出的#13牙,而#12牙存在的20例中有12例(60.0%)存在未萌出的#13牙(Fisher精确检验p = 1.000)。
在左侧,#22牙缺失的15例中有8例(53.3%)存在未萌出的#23牙,而#22牙存在的18例中有11例(61.1%)存在未萌出的#23牙(Fisher精确检验p = 0.733)。
描述性地讲,当两侧合并时,侧切牙缺失的28个牙-侧观察中有16个(57.1%)存在未萌出尖牙,而侧切牙存在的38个观察中有23个(60.5%)存在未萌出尖牙。由于同一患者的双侧观察并非独立观察,因此未对该合并分析赋予推断性p值(表4)。
Table 4. Descriptive relationship between lateral incisor and canine status, both sides pooled.
| Lateral Incisor Status | Canine Erupted | Canine Unerupted | Total |
|---|---|---|---|
| Absent | 12 | 16 | 28 |
| Present | 15 | 23 | 38 |
| Total | 27 | 39 | 66 |
在侧切牙存在的38个牙-侧观察中,5个(13.2%)发现根尖牙根吸收。在20个存在的右侧侧切牙中观察到2个(10.0%)吸收,在18个存在的左侧侧切牙中观察到3个(16.7%)吸收(表5)。
Table 5. Apical root resorption among present lateral incisors ( n = 38).
| Resorption Status | n | % |
|---|---|---|
| No root resorption | 33 | 86.8 |
| Apical root resorption | 5 | 13.2 |
3.2.1. 患者层面侧切牙缺失的患病率
在患者层面,18例患者(54.5%)两侧侧切牙均存在,13例(39.4%)两侧侧切牙均缺失,2例(6.1%)一侧缺失而另一侧存在。因此,33例患者中有15例(45.5%)至少缺失一颗侧切牙(表6)。
Table 6. Patient-level lateral incisor status ( n = 33).
| Status | n | % |
|---|---|---|
| Both present | 18 | 54.5 |
| Both absent | 13 | 39.4 |
| One absent, one present | 2 | 6.1 |
至少缺失一颗侧切牙的患者与两侧侧切牙均存在的患者之间,平均年龄无显著差异(12.1 ± 3.7 vs. 12.8 ± 4.5岁;Mann–Whitney U = 124.0,p = 0.703)。
至少缺失一颗侧切牙的患者比例在17例女性中为9例(52.9%),在16例男性中为6例(37.5%);该差异无统计学意义(Fisher精确检验p = 0.491)(表7)。
Table 7. Age and sex according to presence of at least one absent lateral incisor.
| Variable | At Least One Absent ( n = 15) | Both Present ( n = 18) | Test | p -Value |
|---|---|---|---|---|
| Age, mean ± SD (years) | 12.1 ± 3.7 | 12.8 ± 4.5 | Mann–Whitney U = 124.0 | 0.703 |
| Female, n (%) | 9 (52.9) | 8 (47.1) | Fisher’s exact | 0.491 |
| Male, n (%) | 6 (37.5) | 10 (62.5) |
3.2.2. 唇裂侧别和年龄与牙槽突发现的关系
在牙侧水平,45个受唇裂影响的牙侧中有20个(44.4%)观察到侧切牙缺失,而21个非唇裂侧中有8个(38.1%)。该差异无统计学显著性(χ2=0.048,p=0.827)。
在存在的侧切牙中,25颗受唇裂影响的牙齿中有5颗(20.0%)观察到根尖牙根吸收,而非唇裂侧13颗存在的侧切牙中无一例。Fisher精确检验未显示统计学显著关联(p=0.144)。
在45个受唇裂影响的牙侧中有28个(62.2%)发现未萌出犬齿,而21个非唇裂侧中有11个(52.4%);该差异无统计学显著性(χ2=0.239,p=0.625)。
在患者水平,唇裂侧别与是否存在至少一颗缺失的侧切牙无显著关联(χ2=2.510,df=2,p=0.285),也与是否存在至少一颗未萌出犬齿无显著关联(χ2=1.736,df=2,p=0.420)。
患者年龄与犬齿萌出状态显著相关。至少有一颗未萌出犬齿的患者比两颗犬齿均已萌出的患者更年轻(10.8±3.3岁 vs. 15.1±4.1岁;Mann–Whitney U=53.5,p=0.005)。
年龄与牙根吸收无显著关联。有任何牙根吸收的患者平均年龄为15.7±7.5岁(n=3),而无牙根吸收的患者为12.2±3.7岁(n=30)(Mann–Whitney U=58.5,p=0.414)。该比较受牙根吸收患者数量少的限制(表8)。
Table 8. Summary of supplementary associations.
| Comparison | Unit of Analysis | Statistical Test | Statistic | p -Value |
|---|---|---|---|---|
| Cleft side vs. lateral incisor status | Tooth-side | χ 2 | 0.048 | 0.827 |
| Cleft side vs. root resorption | Present teeth | Fisher’s exact | — | 0.144 |
| Cleft side vs. canine status | Tooth-side | χ 2 | 0.239 | 0.625 |
| Cleft laterality vs. any absent lateral incisor | Patient | χ 2 | 2.510 | 0.285 |
| Cleft laterality vs. any unerupted canine | Patient | χ 2 | 1.736 | 0.420 |
| Age vs. any absent lateral incisor | Patient | Mann–Whitney U | 124.0 | 0.703 |
| Age vs. root resorption | Patient | Mann–Whitney U | 58.5 | 0.414 |
| Age vs. any unerupted canine | Patient | Mann–Whitney U | 53.5 | 0.005 |
3.2.3. 按年龄和性别划分的犬齿状态
在患者水平,至少有一颗未萌出犬齿的患者比例在较年轻年龄组中最高。7–9岁10名患者中有9名(90.0%)存在未萌出犬齿,10–12岁8名患者中有6名(75.0%),13–15岁7名患者中有2名(28.6%),16岁或以上8名患者中有3名(37.5%)(表9)。
Table 9. Canine status by age group.
| Age Group (Years) | Unerupted, n (%) | Erupted, n (%) | Total |
|---|---|---|---|
| 7–9 | 9 (90.0) | 1 (10.0) | 10 |
| 10–12 | 6 (75.0) | 2 (25.0) | 8 |
| 13–15 | 2 (28.6) | 5 (71.4) | 7 |
| ≥16 | 3 (37.5) | 5 (62.5) | 8 |
在女性中,17名患者中有10名(58.8%)至少有一颗未萌出犬齿,而16名男性中有10名(62.5%)。该差异无统计学显著性(Fisher精确检验p=1.000)(表10)。
Table 10. Canine status by sex.
| Sex | Unerupted, n (%) | Erupted, n (%) | Total |
|---|---|---|---|
| Female | 10 (58.8) | 7 (41.2) | 17 |
| Male | 10 (62.5) | 6 (37.5) | 16 |
3.3. 目标2:牙槽突裂尺寸
可获得19个右侧和26个左侧唇裂边缘的轴位近远中裂宽度测量,共45个侧别水平观察。可获得19个右侧和25个左侧唇裂边缘的校正冠状颊腭深度测量,共44个观察。
平均轴位裂宽度为6.29±2.72 mm(中位数5.95 mm;范围2.20–12.50 mm;n=45)。平均校正冠状颊腭深度为8.04±5.30 mm(中位数6.30 mm;范围1.30–27.00 mm;n=44)(表11)。
Table 11. Alveolar cleft measurements by side.
| Measurement | n | Mean ± SD (mm) | Median (mm) | Range (mm) |
|---|---|---|---|---|
| Axial width—right | 19 | 6.44 ± 2.70 | 5.65 | 3.00–12.50 |
| Axial width—left | 26 | 6.18 ± 2.78 | 5.95 | 2.20–11.50 |
| Corrected-coronal depth—right | 19 | 8.26 ± 5.55 | 6.30 | 3.00–27.00 |
| Corrected-coronal depth—left | 25 | 7.88 ± 5.21 | 6.30 | 1.30–27.00 |
按唇裂侧别进行患者水平比较时,对每位患者可用的唇裂侧取轴位裂宽度平均值。单侧左侧唇裂患者的平均轴位宽度为5.51±3.18 mm(n=14),单侧右侧唇裂患者为5.59±1.32 mm(n=7),双侧唇裂患者为7.15±2.65 mm(n=12)。
三组比较未显示统计学显著差异(Kruskal–Wallis H=3.79,df=2,p=0.150)。
在单侧与双侧唇裂的简化比较中,单侧唇裂的平均轴位宽度为5.54±2.67 mm,双侧唇裂为7.15±2.65 mm(Mann–Whitney U=174.5,p=0.072)。
平均轴位裂宽度与患者年龄无显著相关性(Spearman ρ=0.158,n=33,p=0.378)(表12)。
Table 12. Mean patient-level axial cleft width according to cleft laterality.
| Cleft Laterality | n | Mean ± SD (mm) |
|---|---|---|
| Unilateral left | 14 | 5.51 ± 3.18 |
| Unilateral right | 7 | 5.59 ± 1.32 |
| Bilateral | 12 | 7.15 ± 2.65 |
3.3.1. 检查者内部信度
轴向裂隙宽度和校正冠状深度的检查者内部信度均较高。
对于右侧轴向宽度测量,ICC为0.942(95% CI,0.82–0.98;n = 13)。对于右侧校正冠状深度,ICC为0.994(95% CI,0.98–1.00;n = 12)。
对于左侧轴向宽度,ICC为0.970(95% CI,0.89–0.99;n = 11),而左侧校正冠状深度的ICC为0.976(95% CI,0.91–0.99;n = 10)。
在配对测量中,总体ICC为0.974(95% CI,0.95–0.99)。重复测量之间的平均符号差为0.11 mm,95%一致性界限为−0.84至1.06 mm。
分类信度通过对全部33例进行盲法重读评估,重读在足以最小化回忆的间隔后进行。鼻腭管位置的Cohen's kappa为0.86,鼻中隔偏曲为0.88,均表明几乎完全一致(Landis和Koch基准);本数据集中犬齿或侧切牙状态无配对重复读数。
这些结果表明线性裂隙测量的检查者内部一致性较高。
3.3.2. 按性别和邻近解剖发现分组的裂隙宽度
女性平均轴向裂隙宽度为5.94 ± 3.18 mm,男性为6.29 ± 2.28 mm(Mann–Whitney U = 114.5,p = 0.449)。
女性平均校正冠状深度为7.72 ± 5.98 mm,男性为7.56 ± 3.27 mm(Mann–Whitney U = 116.5,p = 0.494)。
轴向裂隙宽度因鼻腭管位置而异(Kruskal–Wallis H = 7.44,p = 0.024)。当鼻腭管居中时,平均轴向宽度为7.82 ± 2.79 mm;当鼻腭管偏向右侧时,为4.87 ± 2.37 mm;当偏向左侧时,为5.93 ± 2.28 mm。
校正冠状深度未因鼻腭管位置而显著差异(H = 2.39,p = 0.302)。
轴向裂隙宽度和校正冠状深度均未因鼻中隔偏曲而显著差异(分别为H = 0.13,p = 0.721和H = 0.05,p = 0.827)(表13)。
Table 13. Cleft width and corrected-coronal depth correlated with sex and with the position of adjacent midline structures.
| Comparison | Test | Statistic | p -Value |
|---|---|---|---|
| Axial width vs. sex | Mann–Whitney U | U = 114.5 | 0.449 |
| Axial width vs. nasopalatine canal position (3 groups) | Kruskal–Wallis | H = 7.44 | 0.024 |
| Axial width vs. nasal septal deviation | Kruskal–Wallis | H = 0.13 | 0.721 |
| Corrected-coronal depth vs. sex | Mann–Whitney U | U = 116.5 | 0.494 |
| Corrected-coronal depth vs. nasopalatine canal position (3 groups) | Kruskal–Wallis | H = 2.39 | 0.302 |
| Corrected-coronal depth vs. nasal septal deviation | Kruskal–Wallis | H = 0.05 | 0.827 |
3.4. 目标3:鼻腭管位置和鼻中隔偏曲
总体而言,鼻腭管偏向右侧者14例(42.4%),居中者11例(33.3%),偏向左侧者8例(24.2%)。在11例归类为居中的鼻腭管中,9例在初次和盲法重复读数中均居中(确认中线),2例在重复读数中被重新分类为侧向偏曲(不确定而非真正居中);所有11例在主要分析中均保留在居中类别中(第4节)。
鼻中隔偏向左侧者21例(63.6%),偏向右侧者11例(33.3%),无明显偏曲者1例(3.0%)(表14)。
Table 14. Overall prevalence of nasopalatine canal position and nasal septal deviation ( n = 33).
| Finding | n | % |
|---|---|---|
| Nasopalatine canal—right | 14 | 42.4 |
| Nasopalatine canal—center | 11 | 33.3 |
| Nasopalatine canal—left | 8 | 24.2 |
| Nasal septum—left | 21 | 63.6 |
| Nasal septum—right | 11 | 33.3 |
| Nasal septum—no deviation | 1 | 3.0 |
鼻腭管位置与裂隙侧别显著相关。Pearson卡方统计量为χ2 = 15.94,自由度为4(p = 0.003),而Fisher–Freeman–Halton精确检验得出p = 0.002(表15)。
Table 15. Nasopalatine canal position according to cleft laterality.
| Cleft Laterality | Canal Right | Canal Center | Canal Left | Total |
|---|---|---|---|---|
| Unilateral left | 9 | 5 | 0 | 14 |
| Unilateral right | 2 | 0 | 5 | 7 |
| Bilateral | 3 | 6 | 3 | 12 |
鼻中隔偏曲也与裂隙侧别显著相关。Pearson卡方统计量为χ2 = 15.00,自由度为4(p = 0.005),而Fisher–Freeman–Halton精确检验得出p = 0.001(表16)。
Table 16. Nasal septal deviation according to cleft laterality.
| Cleft Laterality | Septum Left | Septum Right | No Deviation | Total |
|---|---|---|---|---|
| Unilateral left | 13 | 1 | 0 | 14 |
| Unilateral right | 1 | 6 | 0 | 7 |
| Bilateral | 7 | 4 | 1 | 12 |
在21例单侧病例中,排除居中的鼻腭管后,16例具有明确方向性的鼻腭管位置。在这16例中,14例(87.5%)的鼻腭管位于裂隙对侧,2例(12.5%)位于同侧。
在21例单侧病例中,19例(90.5%)的鼻中隔偏曲朝向裂隙同侧,2例(9.5%)朝向对侧。
3.5 按年龄进行的敏感性分析
由于有6例患者年龄为7–8岁,在排除这些较年轻患者后进行了敏感性分析。所得亚组包括27例年龄9–23岁的患者。
在年龄较大亚组中,侧切牙状态与犬齿萌出状态之间的关联仍无统计学显著性。犬齿未萌出患者与双侧犬齿均已萌出患者之间的年龄差异仍具有显著性,平均年龄分别约为11.9岁和15.7岁(Mann–Whitney U = 37.0,p = 0.010)。
在年龄较大亚组中,31颗现存侧切牙中有3颗(9.7%)观察到牙根吸收,而完整数据集中38颗中有5颗(13.2%)。
在年龄较大亚组中,唇裂侧别与鼻腭管位置之间以及唇裂侧别与鼻中隔偏曲之间的关联也仍具有统计学显著性(精确p = 0.005和p = 0.004)。
总体而言,排除最年轻的患者并未实质性改变主要发现的方向。图5按唇裂侧别总结了这些主要比较:鼻腭管位置(A)和鼻中隔偏曲(B)的两项显著且互为对应的发现、年龄与犬齿萌出状态之间的显著关联(C),以及作为背景展示的唇裂宽度比较无统计学显著性(D)。
[图:按唇裂侧别进行的主要结局比较。(A)鼻腭管位置随唇裂侧别存在显著差异]

4. 讨论
这项对33例腭裂患者的回顾性CBCT分析检查了上颌犬齿与侧切牙状态、牙槽裂的二维尺寸,以及两个相邻中线结构——鼻腭管和鼻中隔——的位置与唇裂侧别、年龄和性别之间的关系。该队列中唇裂侧别的分布(左侧42.4%,双侧36.4%,右侧21.2%)与更广泛的腭裂流行病学文献大体一致,其中左侧单侧受累一直被报告为最常见的表现,尽管出生患病率和表型分布因人群而异[1,2,3,4]。
此处观察到的侧切牙缺失患病率——45.5%的患者至少缺失一颗侧切牙,39.4%的患者缺失双侧侧切牙——处于使用可比牙齿发育不全分类系统的较大腭裂队列所报告的范围之内。使用牙齿发育不全代码,López-Giménez等[10]报告单侧和双侧唇腭裂患者中约51%存在发育不全,其中侧切牙是最常受累的牙齿;而Bartzela等[11]发现荷兰单侧唇裂队列中近一半存在发育不全,约五分之二的患者唇裂侧侧切牙缺失;Haque和Alam[12]则认定上颌侧切牙缺失是跨唇裂严重程度和人群最一致的牙齿异常。因此,本研究发现印证而非偏离了这一文献,进一步强调侧切牙缺失——无论反映的是真正的先天性发育不全还是成像时未能显示(第2.5节)——在近一半腭裂患者中应可预期,无论所研究的具体人群如何。该队列中犬齿状态偏向于未萌出类别(右侧60.6%,左侧54.5%;一颗左侧犬齿,3.0%,为先天性缺失),这与更广泛的认识一致,即邻近牙槽裂的上颌犬齿萌出常受到干扰[25]。然而,关键的是,在本样本中犬齿状态与侧切牙状态无显著关联,无论是按侧别检验(右侧p = 1.000;左侧p = 0.733);由于单个患者的双侧并非独立观察,未对合并的牙侧数据进行推断性检验(第3.2节)。这一阴性发现与Oberoi等[9]一致,他们使用三维CBCT评估骨移植牙槽裂中犬齿萌出路径,同样发现侧切牙先天性缺失与犬齿萌出失败之间无显著关联;两项研究共同提示,唇裂患者的犬齿萌出障碍可能主要由牙槽骨缺损本身和骨移植时机驱动,而非由邻近侧切牙的存在或缺失驱动。这与唇裂人群之外的一般正畸文献形成对比,后者已表明阻生犬齿的初始三维位置——角度、垂直位移、近中分区位置——是萌出成功的主导预后因素[15],再次指向犬齿位置本身而非邻牙状态是更具临床可操作性的变量。
在归类为存在的侧切牙中,13.2%被识别出根尖吸收,这一比例低于有时在伴有阻生犬齿的一般(非裂隙)人群中报告的吸收率;在这些人群中,已显示较薄的唇侧牙槽骨和更向唇侧倾斜的侧切牙牙根会显著增加吸收风险[14],并且犬齿角度和影像学重叠程度是已确立的风险因素[13]。由于本研究未测量牙槽骨厚度或牙根倾斜度,因此无法与这些骨厚度驱动的模型进行直接的机制性比较;此处观察到的相对较低吸收率可能部分反映了若干病例相对年轻的年龄(18.2%在7–8岁时成像,此时牙根成熟尚未可靠完成),这会倾向于低估随着犬齿继续萌出路径而 later 发生的吸收。与这一发育性解释一致,患者年龄与侧切牙状态(p = 0.703)或牙根吸收(p = 0.414)无显著关联,但与犬齿状态显著相关(p = 0.005):年轻患者更可能表现为未萌出犬齿(平均年龄10.8岁)而非已萌出犬齿(平均年龄15.1岁),而性别未显示这种关联(p = 1.000)。这种年龄效应最好由正常生理性萌出时间来解释——上颌犬齿通常在7至11岁之间萌出[5]——而非裂隙特异性病理过程,并强调了当犬齿萌出状态被用作裂隙研究中的结局指标时,按年龄分层解释的重要性。在本样本中,裂隙侧别或受裂隙影响的特定侧别均与侧切牙状态、牙根吸收或犬齿状态无显著关联(所有p > 0.14),提示在本研究可用的样本量下,这些牙槽突异常更多地表现为裂隙表型的普遍特征,而非严格的侧化、机械局限性效应。
从牙列转向裂隙本身的尺寸,本队列的平均轴向裂隙宽度(两侧合并为6.29 ± 2.72 mm)在数量级上与其他基于CBCT的队列中使用三维或多平面测量方案报告的牙槽突裂隙尺寸大致相当,这些方案一贯倾向于容积或多平面评估而非单一线性测量,以捕捉缺损的真实范围[6,7]。裂隙宽度在左侧、右侧和双侧裂隙组之间无显著差异(Kruskal–Wallis p = 0.150),在作为简化两组比较的单侧与双侧裂隙之间也无显著差异(p = 0.072),尽管双侧裂隙在数值上是三组中最宽的(7.15 mm vs. 左侧和右侧单侧裂隙分别为5.51–5.59 mm);裂隙宽度与年龄(Spearman's rho = 0.158,p = 0.378)或性别(p = 0.449)也无显著关联。双侧更宽的非显著趋势在方向上与Regnstrand、Bousiou等(2025)[8]的容积证据一致,他们使用三维CBCT显示双侧牙槽突裂隙表现为两个仅部分独立的缺损,第一和第二植骨侧之间的骨移植填充不均(47% vs. 33%),这意味着即使总体线性宽度相似,双侧裂隙在结构上比单侧裂隙更复杂;本比较中缺乏统计学显著性最可能归因于样本量(12例双侧和21例单侧患者),而非真正缺乏潜在差异,并应在全队列裂隙宽度数据收集完成后重新审视。当裂隙宽度与鼻腭管位置进行检验时,出现了一个进一步的意外关联:轴向宽度在三个管位置组之间有显著差异(Kruskal–Wallis H = 7.44,p = 0.024),中央位置的管与最宽的裂隙相关。然而,这应谨慎解释,因为中央位置的管本身在双侧裂隙病例中更常见(50.0%)而非单侧裂隙(左侧35.7%,右侧0.0%),且双侧裂隙独立地是最宽的侧别组;因此宽度–管位置关联最可能反映了这种与双侧性的共同关系,而非裂隙大小与管位置之间的独立机制联系。在所审查的文献中,似乎没有可比的先前研究直接检验裂隙宽度与鼻腭管或鼻中隔位置之间的相关性,因此这一关联——及其可能的侧别混杂——在此作为初步的、产生假设的观察提出,而非已确立的发现,且冠状深度与任一结构均无相应关联(均p > 0.30)。
本研究最有力且最一致的发现涉及裂隙邻近的两个中线结构。鼻腭管和鼻中隔均与裂隙侧别呈统计学显著相关(精确Fisher–Freeman–Halton检验分别为p = 0.002和p = 0.001),且这两个结构相对于裂隙侧呈相互反向的偏斜:在单侧病例中,87.5%的可评估病例鼻腭管偏离裂隙侧,而90.5%的病例鼻中隔偏向裂隙侧。鼻中隔发现的幅度和方向与Vicente、Wiedel等[19]密切一致,他们采用可比的基于CBCT的裂隙体积及邻近解剖结构评估,报告87%的单侧病例鼻中隔向裂隙或植骨侧弯曲——两个独立队列之间呈现出惊人的一致性。其他基于CBCT的研究同样证实,唇腭裂患者的鼻中隔偏斜显著重于无裂隙或骨性III类对照者[22],且偏斜程度与裂隙严重程度相关[21],进一步支持了本研究发现,即鼻中隔位置与 underlying 裂隙解剖系统性相关而非偶然。值得注意的是,采用直接视觉评分的早期研究报告鼻软骨尖和鼻前棘偏向非裂隙侧[20]——表面上与本研究和Vicente、Wiedel等[19]观察到的鼻中隔体偏斜方向相反。这很可能并非真正的矛盾,而是反映鼻尖、鼻前棘和后/中鼻中隔体是解剖上不同的标志点,在单一的S形或C形畸形中可沿不同甚至相反的轨迹偏斜,这在唇腭裂鼻中隔解剖中已被广泛认识;本研究在轴位和冠状位CBCT上于鼻底水平测量鼻中隔位置,这与临床或照片评估中的鼻尖或鼻前棘位置并不直接等同。鼻腭管的发现拓展了既往基于CBCT的研究,这些研究表明裂隙患者中管道形态本身——不仅是其位置——发生改变,漏斗形、香蕉形和针形管道、更大的孔和管直径以及更短的整体管道长度在裂隙患者中均显著比无裂隙对照者更常见[18];本研究为这一图景增添了侧别特异性维度,显示单侧病例中管道在前上颌内的位置系统性偏离裂隙侧。结合相互反向的鼻中隔发现,这一模式与牙槽和腭部骨缺损对整个前鼻底复合体施加不对称影响相一致,使鼻中隔向缺损侧移位而骨性管道偏离缺损侧,而非两个结构独立受累。从临床角度看,这种相互反向的关系在术前CBCT规划中可能具有至少三个具体方面的实用价值。第一,在规划二次牙槽骨植骨的手术入路和取骨轨迹时,认识到单侧病例中鼻腭管在统计学上更可能位于非裂隙侧,有助于外科医生在术前扫描上预判其位置,并在植骨床预备过程中避免不慎损伤管道,尤其是在管道难以直接追踪的病例中,这一应用与二次牙槽骨植骨的手术规划文献直接相关[8,26]。第二,如果预计患者达到骨骼成熟后行前上颌种植修复,同样的侧别依赖性管道位置可提示种植体截骨更可能或更不可能侵入管道的位置,补充裂隙患者管道形态和直径的现有形态计量学数据[18]。第三,鼻中隔系统性偏向裂隙侧提醒正畸医生和鼻科医生在协调术前正畸或鼻中隔鼻成形术时机时,鼻气道评估应常规伴随该人群的牙槽规划,因为这两个结构似乎由共同机制移位而非独立变化。这些是提出的临床应用而非经过验证的干预措施,每一项都需要前瞻性评估——例如,通过术中导航比较计划与实际管道位置,或将鼻中隔偏斜与主观鼻气道结局相关联——然后才能作为正式的规划指导采纳。
除这些操作层面的应用外,本研究观察到的腭裂侧别与两个独立中线结构位置之间系统性的相互对应关系,具有更广泛的解释意义。如果唇裂和腭裂仅仅是牙槽突和腭部融合的局部失败,那么鼻腭管和鼻中隔——这些位于裂隙边缘之外的结构——没有明显的力学理由会以侧别依赖的相互对应模式发生移位。而它们确实如此——在本队列中表现一致,并与一个独立队列的结果相吻合[19]——提示唇裂和腭裂扰乱了整个前部鼻上颌复合体,而不仅仅是牙槽突段。这一解释得到近期多项CBCT研究的支持,这些研究报告了唇裂队列中鼻中隔、鼻复合体和上颌窦的不对称性[27,28,29,30],尽管如本研究一样,这些结构通常是单独检查,而非与牙槽突裂本身一并评估。近期关于该图景牙槽突侧的CBCT和数字模型证据指向同一方向:缺牙模式仍按唇裂侧别进行报告[31],针对缺牙间隙的尖牙替代方法仍是活跃的研究领域[32],这进一步表明唇裂和腭裂中的牙槽突和中线发现均值得继续开展侧别特异性的特征描述。这并不会降低牙槽突裂的临床重要性,但它提示唇裂诊疗中的CBCT方案应常规在采集裂隙本身的同时捕获鼻腭管和鼻中隔——既作为诊断习惯,也作为在更大队列中进一步检验该模型的手段。
研究局限性
本研究存在若干局限性。第一,样本量相对较小(n = 33),其中单侧右侧裂(n = 7)和双侧裂(n = 12)亚组尤其小。因此,本研究检测中等程度关联的效能可能有限,无统计学显著性的结果不应被解释为不存在关联的证据。若干次要分析为探索性分析,未进行多重比较校正。
第二,回顾性单中心设计限制了结果的普适性。CBCT检查为临床目的而采集,使用了非统一的成像方案,包括视野和CBCT设备的不同,而非在标准化研究方案下进行。
第三,尽管唇裂测量基本完整,但有一个解剖上符合条件的侧别因牙发育不足以识别可靠的测量标志点而无法测量。此外,在数据核查过程中发现一例非裂隙侧的错误测量记录,并将其排除于分析之外。这些问题仅限于个别测量,未改变所报告的结果。
第四,队列包括7–23岁的患者,其中6例为7–8岁。牙发育阶段的差异可能影响对牙根吸收、侧切牙发育和尖牙萌出的判读。排除这些较年轻患者的敏感性分析显示,主要发现——包括唇裂侧别与鼻腭管位置及鼻中隔偏曲之间的关联——仍具有统计学显著性;然而,样本量小限制了排除更细微年龄相关效应的能力。
第五,所有图像评估均由单一检查者完成。线性唇裂测量的检查者内信度极好(合并ICC(A,1) = 0.974;95% CI,0.95–0.99)。对于构成本研究主要显著性发现的两个分类变量——鼻腭管位置和鼻中隔偏曲——检查者内信度通过对全部33例进行盲法重读来评估,重读在足以最小化回忆的间隔后进行,一致性采用Cohen's kappa量化:鼻腭管位置κ = 0.86,鼻中隔偏曲κ = 0.88,均表明几乎完全一致。本回顾性数据集中无法获得尖牙或侧切牙状态的重复分类判读,因此其信度无法以类似方式量化;这仍被记录为一项残余局限性。
第六,中线结构分类的两个方面值得谨慎对待。用于鼻腭管位置和鼻中隔偏曲的解剖中线均根据鼻中隔本身的中点定义(第2.4节);这对鼻腭管(一个独立结构)而言并非循环论证,但这意味着鼻中隔位置描述的是鼻中隔相对于本研究自身参考线的走行,而非相对于完全独立的骨骼轴线的移位。另外,位置无法被确信地判定为偏侧的鼻腭管病例,与鼻腭管确实位于中线的病例一起被归类为居中(第2.5节)。以初次判读与盲法重复判读之间的一致性(第2.6节)作为操作性标准,11个被归类为居中的鼻腭管中,有9个在两次判读中均为居中(确认为中线),而其余2个在重复判读中被重新归类为偏侧(为不确定而非真正居中;第3.4节)。独立定义的骨骼标志点以及前瞻性应用的三分类(居中/不确定/偏侧)将进一步加强未来工作中的这一区分。
未来工作的一个相关方向超出了本分析的范围,即评估该人群中上颌窦黏膜增厚的严重程度,以及其是否累及一个或多个鼻旁窦,作为可能与唇裂侧别相关的邻近面中部附加发现。
第七,将犬齿分类为已萌出或未萌出,并不能区分生理性发育性未萌出与病理性阻生。这一区分在年轻患者中尤为重要,需要纵向临床信息或标准化发育标准,而这些在本回顾性数据集中无法获得。
尽管存在这些局限性,本研究提供了可重复的CBCT测量结果,并确定了唇裂侧别与鼻腭管及鼻中隔位置之间的显著关联。这些发现值得在采用标准化成像方案和纵向评估的更大规模多中心研究中加以证实。
5. 结论
这项回顾性CBCT研究发现,除犬齿萌出与年龄之间的预期关系外,唇裂侧别与牙槽突状态——侧切牙存在、牙根吸收、犬齿萌出或唇裂宽度——之间无显著关联;鉴于样本量有限,这些发现应被视为尚无定论,而非无真实关联的证据。相比之下,鼻腭管位置和鼻中隔偏曲均与唇裂侧别呈显著且相互的关联。由于这两个结构在解剖上与牙槽突裂本身不同,这种分离支持将唇腭裂描述为前部鼻上颌复合体的区域性颅面紊乱,而非孤立的牙槽突缺损,这对术前CBCT规划具有潜在意义。这些发现值得在采用标准化成像方案的更大规模多中心研究中加以证实。
致谢
作者衷心感谢沙特阿拉伯吉达阿卜杜勒阿齐兹国王大学科学研究院长(DSR)根据第(IPP: 976-165-2026)号资助为本项目提供资助和技术支持。此外,作者感谢沙特阿拉伯吉达阿卜杜勒阿齐兹国王大学牙科医院(KAUDH)口腔放射科提供存档CBCT检查资料和成像设施,使本研究得以完成。在本手稿/研究的准备过程中,作者使用Claude(Claude Sonnet 5,Anthropic)进行文献检索支持、统计交叉核对和语言编辑协助。作者已审阅并编辑了输出内容,并对本出版物的内容承担全部责任。
缩略语
本手稿中使用以下缩略语:CBCT,锥形束计算机断层扫描;ICC,组内相关系数;IPDTOC,国际典型口裂围产期数据库;KAUDH,阿卜杜勒阿齐兹国王大学牙科医院;MPR,多平面重建;WHO,世界卫生组织。
补充材料
以下支持信息可从 https://www.mdpi.com/article/10.3390/diagnostics16193140/s1 下载。文件S1:横断面研究STROBE清单。
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机构审查委员会声明
本研究按照《赫尔辛基宣言》进行,并获得沙特阿拉伯吉达阿卜杜勒阿齐兹国王大学牙学院研究伦理委员会批准(方案代码120-05-26,批准日期2026年6月25日)。
知情同意声明
阿卜杜勒阿齐兹国王大学牙学院研究伦理委员会豁免了患者知情同意,因为本研究涉及对去标识化存档CBCT检查的回顾性分析,被归类为不构成人体风险,且无法实现个体再联系。
数据可用性声明
由于回顾性临床影像档案的机构和患者隐私限制,本研究中呈现的数据可应通讯作者要求提供。
利益冲突
作者声明无利益冲突。
资助声明
作者衷心感谢沙特阿拉伯吉达阿卜杜勒阿齐兹国王大学科学研究院长(DSR)根据第(IPP: 976-165-2026)号资助为本项目提供资助和技术支持。
脚注
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参考文献
[内容请查看原文]
关联数据
补充材料
[内容请查看原文]
数据可用性声明
由于回顾性临床影像档案的机构和患者隐私限制,本研究中呈现的数据可应通讯作者要求提供。
查看英文原文▾
Abstract
Background/Objectives: This retrospective study examined, in patients with cleft palate, whether canine eruption status is associated with lateral incisor status, whether cleft width differs by laterality, age, or sex, and whether nasopalatine canal and septal position correlate with cleft laterality. Methods: CBCT examinations of 33 patients were reviewed, including small subgroups of 7 unilateral right-sided, 14 unilateral left-sided and 12 bilateral cases. Lateral incisor and canine status were compared using Fisher’s exact test; cleft width was compared by laterality, age, and sex using the Kruskal– Wallis, Spearman, and Mann–Whitney U tests; and canal and septal position were tested against laterality using the Fisher–Freeman–Halton test, with comparisons repeated excluding the six youngest patients. Results: Canine eruption status was not associated with lateral incisor status (right p = 1.000; left p = 0.733). Root resorption occurred in 13.2% of present lateral incisors, and at least one was absent in 45.5% of patients (all p > 0.14 for age, sex, and side). Canine eruption status was associated with age (unerupted canines younger, 10.8 vs. 15.1 years; p = 0.005). Cleft width did not differ by laterality, age, or sex (all p > 0.14; ICC 0.974). Canal and septal position correlated significantly with laterality (p = 0.002, p = 0.001): the canal deviated away from the cleft side in 87.5% of unilateral cases, and the septum toward it in 90.5%; findings were unchanged after excluding the youngest patients. Intra-examiner reliability for these two variables was almost perfect (Cohen’s κ = 0.86–0.88). Conclusions: Dentoalveolar findings showed no significant association with cleft laterality, apart from the expected age-eruption link, and should be read as inconclusive given the modest sample size. Canal and septal position, by contrast, were significantly and reciprocally correlated with laterality, consistent with cleft palate reflecting a regional craniofacial disturbance rather than an isolated alveolar defect, relevant to pre-surgical planning pending larger-cohort confirmation.
Keywords: cone beam computed tomography, cleft palate, cleft lip, nasopalatine canal, nasal septum, dentoalveolar anomalies, alveolar cleft, cleft laterality
1. Introduction
Orofacial clefts, encompassing cleft lip, cleft palate, and combined cleft lip and palate, are among the most common congenital craniofacial malformations. A recent systematic review and meta-analysis placed the global prevalence at 0.45 per 1000 live births, with figures across individual regional studies commonly falling between approximately 1 in 500 and 1 in 700 live births [1]. Mossey [2] emphasized the value of international, multi-center birth-defects registries for establishing consistent epidemiological associations across populations with differing genetic and environmental backgrounds. Data pooled from the related International Perinatal Database of Typical Oral Clefts (IPDTOC) demonstrate a six-fold variation in the birth prevalence of cleft lip with or without cleft palate across populations and a three-fold variation for isolated cleft palate [3], and regional reviews focused on Arab populations report an average orofacial-cleft prevalence of approximately 1.1 per 1000 live births, with cleft palate identified as the predominant subtype in several countries of the region [4]. Beyond the facial and nasal deformity, itself, orofacial clefts are consistently associated with a constellation of Dento-alveolar disturbances in the cleft region, including tooth agenesis, malformed or displaced teeth, altered eruption sequences, and structural anomalies of the alveolar bone that together complicate long-term orthodontic and surgical rehabilitation [5].
The alveolar cleft is a bony defect of the maxillary alveolar process that normally houses the roots of the lateral incisor and canine, and it is present in the majority of patients with cleft lip and/or palate [1]. Because this defect can disturb Dento-alveolar growth, tooth eruption, and periodontal support in the adjacent dentition, accurate three-dimensional characterization of its dimensions is essential for surgical and orthodontic planning. Two-dimensional radiographs underestimate bucco-lingual bone loss and cannot reliably depict the true architecture of the defect, which has driven a shift toward CBCT as the imaging modality of choice for cleft assessment. Comparative work evaluating different CBCT-based methods of quantifying alveolar cleft defects has confirmed that three-dimensional volumetric assessment is more accurate than any single-plane method [6], a conclusion echoed by a study comparing computer-simulation and water-displacement approaches to preoperative cleft-volume measurement on CBCT [7].
Cleft laterality itself appears to influence graft outcome and residual defect volume: a three-dimensional volumetric study of bilateral alveolar clefts managed with staged, two-step bone grafting found that the first-grafted site achieved significantly greater bone fill (47%) than the second-grafted site (33%), and that cleft volume on the still-ungrafted contralateral side did not change materially after the first surgery—evidence that bilateral clefts behave as two at least partly independent defects rather than a single symmetric entity, with direct relevance to how cleft laterality should be analyzed as a variable [8]. Corrected sagittal reconstruction, reoriented perpendicular to the dental arch rather than to the true anatomical plane, has become a standard adjunct to the axial view in these protocols because it allows unobstructed visualization of the cleft margins along the long axis of the adjacent roots [9].
The maxillary lateral incisor is the tooth most frequently affected by developmental disturbance in patients with cleft lip and palate, because its dental bud lies directly at or near the cleft margin. Using the Tooth Agenesis Code, López-Giménez et al. [10] reported agenesis prevalence of approximately 51% in both unilateral and bilateral cleft lip and palate in a Spanish cohort, with the lateral incisor the tooth most frequently missing, particularly within the cleft quadrant. Bartzela et al. [11] similarly found agenesis in nearly half of subjects in a Dutch cohort of complete unilateral cleft lip and palate patients, with the cleft-side lateral incisor absent in roughly two of five patients. A broader review of dental anomalies in cleft populations corroborated missing maxillary lateral incisors as the single most consistent finding across cleft severities and ethnicities, alongside supernumerary teeth, microdontia, and taurodontism [12].
Root resorption of a present lateral incisor may occur when it is positioned close to a displaced or erupting canine—a well-described phenomenon in the general orthodontic literature, where Alqerban et al. [13] synthesized the risk factors for lateral incisor root resorption caused by an adjacent impacted canine, including canine angulation, degree of radiographic overlap, and buccopalatal position. A large, more recent CBCT-based retrospective study of 305 patients with unilateral maxillary impacted canines confirmed that a thinner labial alveolar plate and a more labially inclined lateral incisor root are independently associated with a greater degree of resorption, and that resorption prevalence differs by the canine’s buccopalatal position [14]. In the cleft population specifically, the coexistence of a bony defect, a frequently rotated or displaced lateral incisor, and an atypical canine eruption path creates a distinct anatomical context in which this resorptive process has not been as systematically documented—a gap the present study addresses by classifying lateral incisor status as present, absent, or root-resorbed.
The maxillary canine in cleft patients follows an eruption pathway frequently altered by the adjacent bony defect, the presence or absence of the lateral incisor, and the timing of secondary alveolar bone grafting relative to root development. Oberoi et al. [9] found no significant association between congenital absence of the lateral incisor and canine root completion or eruption failure in a three-dimensional evaluation of the canine eruption pathway in bone-grafted alveolar clefts, whereas other investigators have reported an association between lateral incisor agenesis and an increased rate of canine impaction, albeit with low certainty of evidence. A systematic review by Grisar et al. [15] found that the initial three-dimensional position of impacted maxillary canines—angulation, vertical displacement, and mesial sector position—predicted treatment outcome across nearly 1600 impacted canines more strongly than eruption status alone. Importantly for interpreting eruption status in a mixed-dentition or early-adolescent cleft sample, an unerupted canine at the time of imaging does not necessarily indicate pathological impaction: physiological eruption of the maxillary canine typically occurs between 7 and 11 years of age, and a canine still descending along a normal path in a young patient should be classified as developing rather than impacted [5]. This distinction supports framing canine status in the present study as a descriptive, prevalence-based variable—erupted or unerupted—rather than a clinical diagnosis of impaction.
The nasopalatine (incisive) canal is a midline structure connecting the floor of the nasal cavity to the anterior hard palate, posterior to the maxillary central incisors. In non-cleft populations, CBCT morphometric studies describe substantial variation in canal shape, length, and diameter, with males generally exhibiting longer, wider canals than females [16], and morphologic canal change has been documented in relation to alveolar bone resorption and implant planning [17]. A study directly comparing the nasopalatine canal in patients with and without cleft palate, using CBCT exams evaluated in coronal, sagittal, and axial reformats, found funnel-, banana-, and needle-shaped canals significantly more frequent in cleft patients, together with a significantly larger nasopalatine foramen and canal diameter but a significantly shorter overall canal length compared with non-cleft controls [18]. A separate CBCT investigation that specifically evaluated cleft volume alongside adjacent anatomical structures found that the incisive foramen was not visible in 71% of bilateral cleft cases, significantly less often than in unilateral clefts, indicating that the cleft defect itself may directly involve or obliterate the canal’s oral opening in more severe presentations [19]. These findings collectively support the premise that the disrupted embryological fusion underlying the alveolar cleft also reshapes this adjacent midline canal, reinforcing the clinical relevance of characterizing the canal’s proximity to the cleft margin when planning bone grafting or implant-based rehabilitation.
Distortion of the nasal septum is one of the most consistent secondary deformities associated with cleft lip and palate, arising from both the primary embryological defect and the unopposed muscular pull exerted across the clefted lip and alveolus before surgical repair. An early study using direct visual scoring demonstrated that nasal septal deviation occurs significantly more frequently in individuals with cleft lip and palate than in non-cleft controls, with the cartilaginous nasal tip and anterior nasal spine both tending to deviate toward the non-cleft side [20]. Using CBCT, a widely cited otolaryngology study of nasal septal deviation in cleft palate and/or alveolus patients found that the degree of deviation correlated significantly with cleft severity [21], while a subsequent three-dimensional CBCT analysis quantified septal deviation angle and linear displacement at the anterior nasal spine, posterior nasal spine, and their midpoint, finding significantly greater deviation in unilateral cleft lip and palate patients than in skeletal Class III non-cleft controls [22]. The combined cleft-volume and adjacent-structures CBCT study noted above similarly found the nasal septum curved toward the cleft or graft side in 87% of unilateral cases, and additionally found the inferior turbinate significantly smaller on the cleft side than the non-cleft side [19].
Collectively, this literature establishes each variable relevant to the present study—alveolar cleft morphometrics, lateral incisor status, canine eruption pattern, nasopalatine canal morphology, and nasal septal deviation—as a recognized, independently investigated feature of the cleft lip and palate phenotype. However, few if any published studies have combined all of these parameters within a single cohort using a standardized CBCT protocol incorporating both axial and corrected coronal views, and fewer still have examined how lateral incisor status (present, missing, or root-resorbed) relates jointly to canine eruption pattern, cleft dimensions, and the position of two adjacent midline structures—the nasopalatine canal and the nasal septum—within the same patients. This integrated, prevalence-and-correlation approach—rather than a further single-structure analysis—is the specific contribution of the present study.
This scope also follows from the imaging modality: CBCT captures mineralized, bony structures well, but it does not reliably show the soft-tissue lip. CBCT-based bone-assessment protocols in cleft patients have therefore focused specifically on the alveolar and palatal skeleton [23,24]. For that reason, we scoped the present study to cleft palate—the bony component CBCT actually visualizes—rather than to cleft lip and palate as a combined soft- and hard-tissue diagnosis.
1.1. Objectives
The general objective of this study was to evaluate, using cone beam computed tomography, the Dento-alveolar and anatomical characteristics of patients with cleft palate and their statistical relationship to cleft laterality. The specific objectives were as follows:
To determine whether maxillary canine eruption status (erupted vs. unerupted) is statistically associated with lateral incisor status (present vs. absent) in patients with cleft palate, tested using Fisher’s exact test.
To measure the two-dimensional alveolar cleft width—the mesio-distal width on the axial plane and the bucco palatal depth on the corrected coronal plane—and to compare cleft width between unilateral and bilateral cleft cases.
To determine the prevalence of nasopalatine canal position and nasal septal deviation, and to test their statistical correlation with cleft laterality (unilateral right, unilateral left, or bilateral).
1.2. Hypotheses
Null Hypothesis (H0): Maxillary canine eruption status is not significantly associated with lateral incisor status; alveolar cleft width does not differ significantly between unilateral and bilateral cleft cases; and nasopalatine canal position and nasal septal deviation are not significantly correlated with cleft laterality.
Alternative Hypothesis (H1): Maxillary canine eruption status is significantly associated with lateral incisor status, such that an absent lateral incisor is associated with a different rate of canine non-eruption; alveolar cleft width differs significantly between unilateral and bilateral cleft cases; and nasopalatine canal position and nasal septal deviation are significantly correlated with cleft laterality.
2. Materials and Methods
2.1. Study Design and Setting
This retrospective cross-sectional study was conducted using CBCT examinations archived in the Oral Radiology Department, King Abdulaziz University Dental Hospital (KAUDH), Jeddah, Saudi Arabia. This report follows the STROBE (Strengthening the Reporting of Observational Studies in Epidemiology) guidelines for cross-sectional studies; the completed STROBE checklist is provided as a supplementary file, File S1.
2.2. Case Selection
Cases were identified through a retrospective search of the Oral Radiology Department archive for patients with cleft palate who had undergone CBCT imaging as part of routine multidisciplinary cleft care between August 2024 and June 2026.
To be included, a case needed a clinical diagnosis of cleft lip and/or palate, an archived CBCT examination acquired for routine multidisciplinary cleft care, and image quality and field of view sufficient to visualize the alveolar cleft together with the nasopalatine canal and nasal septum. Three situations led to exclusion: an alveolar cleft that had already been surgically closed before the CBCT was taken, a suspected cleft that turned out on review to be an isolated midline diastema, and any case where clinical and radiographic review did not confirm cleft palate. Since CBCT scan detects only bone structures, we studied only cleft palate without any assessment of lip cleft.
Thirty-six CBCT examinations initially met the search criteria. Three examinations were excluded before analysis: one because the alveolar cleft had already been surgically closed before CBCT acquisition, one because the finding initially interpreted as a cleft represented an isolated midline diastema, and one because review of the clinical and radiographic records confirmed that the patient did not have a cleft palate. The remaining 33 examinations constituted the eligible analytic cohort (Figure 1). We did not perform an a priori sample-size calculation. The study simply included every eligible examination available in the archive over the study period, which fits the exploratory, retrospective nature of this analysis. Section 4 discusses the resulting sample size and the limited power this leaves for the smaller subgroups.
[图:Case selection flow diagram: examinations identified, reasons for exclusion, and the resulting eligible analytic cohort.]

The following variables were available for the eligible cohort: sex, age at imaging, cleft laterality, maxillary lateral incisor status, maxillary canine status, nasopalatine canal position, and nasal septal deviation.
Because tooth development may be incomplete in younger patients, particular caution was applied to the interpretation of root resorption and eruption status. Six patients (18.2%) were 7–8 years of age at the time of imaging. These patients were retained in the primary analyses, but findings dependent on root development or physiological eruption timing were interpreted with consideration of developmental stage.
When more than one eligible CBCT examination was available for the same patient, the examination selected for analysis was the earliest eligible pretreatment examination that provided adequate visualization of the structures required for the study. When multiple examinations were available around the same treatment milestone, the examination with more complete dental development and adequate image quality was preferentially selected.
2.3. CBCT Acquisition and Image Evaluation
CBCT examinations had been acquired using equipment available in the Oral Radiology Department during the study period. Most examinations were obtained using a KaVo 3D eXam® CBCT unit (KaVo Dental GmbH, Biberach, Germany), while a subset had been acquired using an i-CAT® unit (Imaging Sciences International/KaVo Kerr, Hatfield, PA, USA).
For examinations acquired using the KaVo 3D eXam unit, the standardized exposure parameters were 90 kV, 6.3 mA, and an exposure time of 8.7 s, with a dose–area product of 509 mGy/cm2. Because the study used a retrospective clinical archive, field of view was not uniform across examinations. However, all included examinations encompassed the bilateral maxilla, allowing assessment of both the cleft-affected and contralateral regions. The majority of examinations used an isotropic voxel size of 0.3 mm.
CBCT datasets were reviewed using OnDemand3D imaging software (Cybermed Inc., Seoul, South Korea). Images were evaluated using multiplanar reconstruction (MPR) in axial, sagittal, and coronal planes (Figure 2). Panoramic reconstructions were also reviewed when useful for assessment of tooth presence, eruption status, and overall dental anatomy.
[图:Representative CBCT reconstructions, multiplanar views, and panoramic reconstruction used for image assessment. ( A ) Th]

Patient age and sex were obtained from the clinical imaging records and cross-checked against the archived patient information.
2.4. Measurement Protocol and Reference Planes
A standardized image-orientation protocol was used for all linear measurements.
For sagittal assessment, the horizontal reference line was oriented parallel to the floor of the hard palate. For axial and coronal assessment, the anatomical midline was defined using the midpoint of the nasal septum. The anatomical midline was used rather than the dental midline because cleft-related displacement of the anterior dentition may alter the position of the dental midline. Because this same septal reference was also used to classify nasal septal position (Section 2.5), the nasopalatine canal—an independent structure—was assessed against this midline without circularity, but nasal septal position could not be assessed against a fully independent skeletal landmark in this retrospective dataset; this is addressed explicitly as a limitation (Section 4).
Two linear cleft measurements were evaluated:
Axial mesiodistal cleft width: measured on the axial CBCT reconstruction at the coronal third of the alveolar process, approximately 1 mm apical to the alveolar crest. The measurement represented the mesiodistal distance across the alveolar cleft between the central incisor and the adjacent lateral incisor or canine bordering the defect (Figure 3).
[图:Representative CBCT images demonstrating cleft width measurement in a unilateral (right-sided) cleft case. ( A ) Axial C]

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Corrected-coronal buccopalatal cleft depth: measured on a corrected coronal reconstruction at the mid-palatal level. The corrected coronal plane was oriented perpendicular to the dental arch and positioned to pass through the relevant adjacent tooth structures. The measurement was obtained distal to the root of the lateral incisor when the lateral incisor was present or relative to the canine when the lateral incisor was absent. The corrected coronal reconstruction was used to obtain a plane perpendicular to the relevant dental anatomy and to minimize measurement distortion caused by the three-dimensional orientation of the cleft.
In bilateral cleft cases in which the two cleft spaces formed a continuous defect, the defect was evaluated relative to the anatomical midline and the measurements were recorded separately for the right and left components where the anatomy allowed side-specific assessment.
Axial cleft-width measurements were available for 45 cleft-side observations. Corrected-coronal buccopalatal depth measurements were available for 44 cleft-side observations. A “cleft-side observation” refers to one measurable cleft margin; unilateral patients contributed one such observation and bilateral patients could contribute up to two, which is why these counts exceed the 33-patient cohort.
2.5. Variables and Classification
The following variables were recorded for each patient:
sex;
age at CBCT imaging;
cleft laterality (unilateral right, unilateral left, or bilateral);
maxillary lateral incisor status for teeth #12 and #22;
maxillary canine status for teeth #13 and #23;
nasopalatine canal position; and
nasal septal deviation.
Maxillary lateral incisor status
Each maxillary lateral incisor was classified as follows:
present without apical root resorption;
present with apical root resorption; or
absent at the time of imaging.
For statistical analyses, lateral incisor status was further dichotomized as present or absent. Among present lateral incisors, root resorption was analyzed as a separate binary variable.
The term absent refers to failure to identify the permanent lateral incisor at the time of CBCT examination and does not necessarily establish congenital agenesis, particularly in younger patients. In cases in which a retained primary lateral incisor could not be confidently distinguished from a developing permanent successor, the permanent lateral incisor was recorded as absent for the radiographic time point rather than being interpreted as confirmed congenital agenesis (Figure 4).
[图:Representative CBCT images demonstrating the status of the maxillary lateral incisor adjacent to the cleft. ( A ) Correc]

Maxillary canine status
Each maxillary canine was classified as either erupted or unerupted.
The unerupted category included canines that remained intraosseous at the time of CBCT examination. This classification was deliberately used instead of “impacted” because a single CBCT examination cannot reliably distinguish pathological impaction from normal developmental non-eruption, particularly in younger patients.
Nasopalatine canal position
The nasopalatine canal was classified according to its position relative to the anatomical midline as follows:
deviated toward the right;
centered/midline; or
deviated toward the left.
When the canal could not be confidently localized, the anatomical midline was used as the reference and the canal was classified as centered rather than assigning an uncertain directional deviation.
Nasal septal deviation
Nasal septal position was classified as follows:
deviated toward the right;
deviated toward the left; or
no appreciable deviation.
Because the anatomical midline above (Section 2.4) was itself derived from the nasal septum, this variable describes the septum’s course relative to the study’s own reference rather than displacement validated against a wholly independent skeletal axis; this is discussed as a limitation in Section 4.
2.6. Examiner Reliability and Data Quality Control
All image assessments were performed by a single oral and maxillofacial radiologist (H.S.).
To assess intra-examiner reliability, a subset of examinations was re-evaluated after an interval sufficient to minimize recall of the initial measurements. The repeated assessments included axial cleft width and corrected-coronal buccopalatal depth measurements. The number of repeated cases ranged from 10 to 13 for each measurement category.
Reliability was assessed using a two-way mixed-effects intraclass correlation coefficient for absolute agreement and single measurements [ICC(A,1)]. Mean signed differences between the first and second measurements and 95% limits of agreement were also calculated.
All measurements were subsequently checked against the original CBCT examinations and source data before statistical analysis. Any obvious data-entry discrepancies were resolved by returning to the original CBCT dataset and recording the verified measurement.
For nasopalatine canal position and nasal septal deviation—the two categorical variables underlying the principal significant findings of this study—intra-examiner reliability was additionally assessed via a blinded re-read of all 33 cases, with agreement quantified using Cohen’s kappa: κ = 0.86 for canal position and κ = 0.88 for septal deviation (both almost-perfect agreement; see Section 3.3.1). Repeat categorical readings were not available for canine or lateral incisor status in this retrospective dataset.
2.7. Statistical Analysis
Canine and lateral incisor status belong to a specific tooth and side, so we analyzed these two variables at the tooth-side level. Cleft laterality, cleft width, nasopalatine canal position, and nasal septal deviation, by contrast, are properties of the patient as a whole rather than of one tooth, so we analyzed these at the patient level. We kept this distinction throughout the analyses below. Descriptive statistics were calculated for all variables. Categorical variables were summarized using frequencies and percentages. Continuous variables were summarized using the mean, standard deviation, median, and range.
For Objective 1, the association between ipsilateral lateral incisor status (present vs. absent) and canine eruption status (erupted vs. unerupted) was assessed separately for the right side (#12/#13) and left side (#22/#23) using Fisher’s exact test. Because right and left tooth-side observations from the same patient are not statistically independent, pooled bilateral tooth-side data were presented descriptively but were not subjected to an additional inferential Fisher’s exact test.
At the patient level, chi-square tests were used to assess the relationship between cleft laterality and the presence of at least one absent lateral incisor and between cleft laterality and the presence of at least one unerupted canine. Fisher’s exact test was used to evaluate the relationship between sex and the presence of at least one absent lateral incisor.
Age was compared between patients with and without at least one absent lateral incisor, with and without root resorption, and with at least one unerupted canine versus both canines erupted using the Mann–Whitney U test.
The relationship between the specific cleft-affected side and tooth-level findings was assessed descriptively and, where appropriate, using Fisher’s exact test because bilateral cases contribute observations from both sides and therefore do not represent independent patient-level observations.
For Objective 2, axial cleft width and corrected-coronal buccopalatal depth were summarized by side. For comparison by cleft laterality, axial width was averaged across available cleft sides for each patient, and the resulting patient-level values were compared among unilateral-left, unilateral-right, and bilateral cleft groups using the Kruskal–Wallis test. A simplified unilateral-versus-bilateral comparison was additionally performed using the Mann–Whitney U test. The relationship between patient age and mean axial cleft width was assessed using Spearman’s rank correlation coefficient.
For Objective 3, the associations between nasopalatine canal position and cleft laterality and between nasal septal deviation and cleft laterality were assessed using the Fisher–Freeman–Halton exact test because of the sparse cell counts in the 3 × 3 contingency tables. Pearson chi-square statistics were also calculated as reference statistics. Among unilateral cases, the direction of nasopalatine canal position and nasal septal deviation relative to the cleft side was summarized descriptively as same-side or opposite-side deviation.
A two-sided p-value < 0.05 was considered statistically significant. Because several analyses were exploratory and the study was based on a relatively small retrospective cohort, p-values were interpreted in the context of effect direction, sample size, and measurement availability rather than as definitive evidence of absence of association.
Statistical analyses were performed using Python version 3.11 with the pandas and SciPy libraries.
During preparation of this manuscript, the author used an AI-based writing and analysis assistant Claude Sonnet 5 (Anthropic) for literature search support, statistical cross-checking, and language editing assistance. The authors have reviewed and edited the output and take full responsibility for the content of this publication.
3. Results
3.1. Sample Characteristics
Of the 36 CBCT examinations initially identified, 3 were excluded (Section 2.2 details the inclusion/exclusion criteria and reasons); the final analytic cohort comprised 33 patients (Figure 1).
The cohort included 17 females (51.5%) and 16 males (48.5%). The mean age at imaging was 12.5 ± 4.1 years, with a median of 12.0 years and a range of 7–23 years. Six patients (18.2%) were 7–8 years old at imaging.
Unilateral left-sided clefts were the most common presentation (n = 14, 42.4%), followed by bilateral clefts (n = 12, 36.4%) and unilateral right-sided clefts (n = 7, 21.2%) (Table 1).
Table 1. Sample characteristics of the study cohort ( n = 33).
| Characteristic | n | % |
|---|---|---|
| Female | 17 | 51.5 |
| Male | 16 | 48.5 |
| Age 7–8 years | 6 | 18.2 |
| Age ≥9 years | 27 | 81.8 |
| Unilateral left cleft | 14 | 42.4 |
| Bilateral cleft | 12 | 36.4 |
| Unilateral right cleft | 7 | 21.2 |
3.2. Objective 1: Maxillary Lateral Incisor and Canine Status
For tooth #12, 18 of 33 patients (54.5%) had a lateral incisor without apical root resorption, 2 (6.1%) had apical root resorption, and 13 (39.4%) had no identifiable permanent lateral incisor at the time of imaging.
For tooth #22, 15 patients (45.5%) had a lateral incisor without apical root resorption, 3 (9.1%) had apical root resorption, and 15 (45.5%) had no identifiable permanent lateral incisor.
When both sides were considered descriptively, 28 of 66 tooth-side observations (42.4%) were classified as absent and 38 (57.6%) as present (Table 2).
Table 2. Maxillary lateral incisor status by tooth ( n = 33).
| Status | Tooth #12, n (%) | Tooth #22, n (%) |
|---|---|---|
| Present without root resorption | 18 (54.5) | 15 (45.5) |
| Present with apical root resorption | 2 (6.1) | 3 (9.1) |
| Absent | 13 (39.4) | 15 (45.5) |
Maxillary canine status was classified as erupted or unerupted. For tooth #13, 20 patients (60.6%) had an unerupted canine and 13 (39.4%) had an erupted canine. For tooth #23, 19 patients (57.6%) had an unerupted canine and 14 (42.4%) had an erupted canine. No congenitally absent maxillary canine was identified in the cohort (Table 3).
Table 3. Maxillary canine eruption status by tooth ( n = 33).
| Status | Tooth #13, n (%) | Tooth #23, n (%) |
|---|---|---|
| Unerupted | 20 (60.6) | 19 (57.6) |
| Erupted | 13 (39.4) | 14 (42.4) |
On the right side, an unerupted #13 was present in 8 of 13 cases (61.5%) in which #12 was absent, compared with 12 of 20 cases (60.0%) in which #12 was present (Fisher’s exact p = 1.000).
On the left side, an unerupted #23 was present in 8 of 15 cases (53.3%) in which #22 was absent, compared with 11 of 18 cases (61.1%) in which #22 was present (Fisher’s exact p = 0.733).
Descriptively, when both sides were pooled, 16 of 28 tooth-side observations with an absent lateral incisor (57.1%) had an unerupted canine, compared with 23 of 38 observations with a present lateral incisor (60.5%). Because the two sides from an individual patient are not independent observations, no inferential p-value was assigned to this pooled analysis (Table 4).
Table 4. Descriptive relationship between lateral incisor and canine status, both sides pooled.
| Lateral Incisor Status | Canine Erupted | Canine Unerupted | Total |
|---|---|---|---|
| Absent | 12 | 16 | 28 |
| Present | 15 | 23 | 38 |
| Total | 27 | 39 | 66 |
Among the 38 tooth-side observations in which the lateral incisor was present, apical root resorption was identified in 5 (13.2%). Resorption was observed in 2 of 20 present right lateral incisors (10.0%) and 3 of 18 present left lateral incisors (16.7%) (Table 5).
Table 5. Apical root resorption among present lateral incisors ( n = 38).
| Resorption Status | n | % |
|---|---|---|
| No root resorption | 33 | 86.8 |
| Apical root resorption | 5 | 13.2 |
3.2.1. Patient-Level Prevalence of Missing Lateral Incisors
At the patient level, 18 patients (54.5%) had both lateral incisors present, 13 (39.4%) had both lateral incisors absent, and 2 (6.1%) had one absent and one present lateral incisor. Thus, at least one lateral incisor was absent in 15 of 33 patients (45.5%) (Table 6).
Table 6. Patient-level lateral incisor status ( n = 33).
| Status | n | % |
|---|---|---|
| Both present | 18 | 54.5 |
| Both absent | 13 | 39.4 |
| One absent, one present | 2 | 6.1 |
Mean age did not differ significantly between patients with at least one absent lateral incisor and those with both lateral incisors present (12.1 ± 3.7 vs. 12.8 ± 4.5 years; Mann–Whitney U = 124.0, p = 0.703).
The proportion of patients with at least one absent lateral incisor was 9 of 17 females (52.9%) and 6 of 16 males (37.5%); this difference was not statistically significant (Fisher’s exact p = 0.491) (Table 7).
Table 7. Age and sex according to presence of at least one absent lateral incisor.
| Variable | At Least One Absent ( n = 15) | Both Present ( n = 18) | Test | p -Value |
|---|---|---|---|---|
| Age, mean ± SD (years) | 12.1 ± 3.7 | 12.8 ± 4.5 | Mann–Whitney U = 124.0 | 0.703 |
| Female, n (%) | 9 (52.9) | 8 (47.1) | Fisher’s exact | 0.491 |
| Male, n (%) | 6 (37.5) | 10 (62.5) |
3.2.2. Relationship of Cleft Laterality and Age with Dentoalveolar Findings
At the tooth-side level, lateral incisor absence was observed in 20 of 45 cleft-affected sides (44.4%) compared with 8 of 21 non-cleft sides (38.1%). This difference was not statistically significant (χ2 = 0.048, p = 0.827).
Among present lateral incisors, apical root resorption was observed in 5 of 25 cleft-affected teeth (20.0%) compared with none of 13 present lateral incisors on non-cleft sides. Fisher’s exact test did not demonstrate a statistically significant association (p = 0.144).
An unerupted canine was identified on 28 of 45 cleft-affected sides (62.2%) compared with 11 of 21 non-cleft sides (52.4%); this difference was not statistically significant (χ2 = 0.239, p = 0.625).
At the patient level, cleft laterality was not significantly associated with the presence of at least one absent lateral incisor (χ2 = 2.510, df = 2, p = 0.285) or with the presence of at least one unerupted canine (χ2 = 1.736, df = 2, p = 0.420).
Patient age was significantly associated with canine eruption status. Patients with at least one unerupted canine were younger than patients with both canines erupted (10.8 ± 3.3 vs. 15.1 ± 4.1 years; Mann–Whitney U = 53.5, p = 0.005).
Age was not significantly associated with root resorption. Patients with any root resorption had a mean age of 15.7 ± 7.5 years (n = 3), compared with 12.2 ± 3.7 years (n = 30) among those without resorption (Mann–Whitney U = 58.5, p = 0.414). This comparison was limited by the small number of patients with root resorption (Table 8).
Table 8. Summary of supplementary associations.
| Comparison | Unit of Analysis | Statistical Test | Statistic | p -Value |
|---|---|---|---|---|
| Cleft side vs. lateral incisor status | Tooth-side | χ 2 | 0.048 | 0.827 |
| Cleft side vs. root resorption | Present teeth | Fisher’s exact | — | 0.144 |
| Cleft side vs. canine status | Tooth-side | χ 2 | 0.239 | 0.625 |
| Cleft laterality vs. any absent lateral incisor | Patient | χ 2 | 2.510 | 0.285 |
| Cleft laterality vs. any unerupted canine | Patient | χ 2 | 1.736 | 0.420 |
| Age vs. any absent lateral incisor | Patient | Mann–Whitney U | 124.0 | 0.703 |
| Age vs. root resorption | Patient | Mann–Whitney U | 58.5 | 0.414 |
| Age vs. any unerupted canine | Patient | Mann–Whitney U | 53.5 | 0.005 |
3.2.3. Canine Status by Age and Sex
At the patient level, the proportion of patients with at least one unerupted canine was highest in the younger age groups. An unerupted canine was present in 9 of 10 patients aged 7–9 years (90.0%), 6 of 8 patients aged 10–12 years (75.0%), 2 of 7 patients aged 13–15 years (28.6%), and 3 of 8 patients aged 16 years or older (37.5%) (Table 9).
Table 9. Canine status by age group.
| Age Group (Years) | Unerupted, n (%) | Erupted, n (%) | Total |
|---|---|---|---|
| 7–9 | 9 (90.0) | 1 (10.0) | 10 |
| 10–12 | 6 (75.0) | 2 (25.0) | 8 |
| 13–15 | 2 (28.6) | 5 (71.4) | 7 |
| ≥16 | 3 (37.5) | 5 (62.5) | 8 |
Among females, 10 of 17 patients (58.8%) had at least one unerupted canine, compared with 10 of 16 males (62.5%). This difference was not statistically significant (Fisher’s exact p = 1.000) (Table 10).
Table 10. Canine status by sex.
| Sex | Unerupted, n (%) | Erupted, n (%) | Total |
|---|---|---|---|
| Female | 10 (58.8) | 7 (41.2) | 17 |
| Male | 10 (62.5) | 6 (37.5) | 16 |
3.3. Objective 2: Alveolar Cleft Dimensions
Axial mesiodistal cleft-width measurements were available for 19 right-sided and 26 left-sided cleft margins, giving 45 side-level observations. Corrected-coronal buccopalatal depth measurements were available for 19 right-sided and 25 left-sided cleft margins, giving 44 observations.
The mean axial cleft width was 6.29 ± 2.72 mm (median, 5.95 mm; range, 2.20–12.50 mm; n = 45). The mean corrected-coronal buccopalatal depth was 8.04 ± 5.30 mm (median, 6.30 mm; range, 1.30–27.00 mm; n = 44) (Table 11).
Table 11. Alveolar cleft measurements by side.
| Measurement | n | Mean ± SD (mm) | Median (mm) | Range (mm) |
|---|---|---|---|---|
| Axial width—right | 19 | 6.44 ± 2.70 | 5.65 | 3.00–12.50 |
| Axial width—left | 26 | 6.18 ± 2.78 | 5.95 | 2.20–11.50 |
| Corrected-coronal depth—right | 19 | 8.26 ± 5.55 | 6.30 | 3.00–27.00 |
| Corrected-coronal depth—left | 25 | 7.88 ± 5.21 | 6.30 | 1.30–27.00 |
For patient-level comparison by cleft laterality, axial cleft width was averaged across available cleft sides for each patient. Mean axial width was 5.51 ± 3.18 mm among patients with unilateral left-sided clefts (n = 14), 5.59 ± 1.32 mm among patients with unilateral right-sided clefts (n = 7), and 7.15 ± 2.65 mm among patients with bilateral clefts (n = 12).
The three-group comparison did not demonstrate a statistically significant difference (Kruskal–Wallis H = 3.79, df = 2, p = 0.150).
In the simplified comparison of unilateral versus bilateral clefts, mean axial width was 5.54 ± 2.67 mm for unilateral clefts and 7.15 ± 2.65 mm for bilateral clefts (Mann–Whitney U = 174.5, p = 0.072).
Mean axial cleft width was not significantly correlated with patient age (Spearman’s ρ = 0.158, n = 33, p = 0.378) (Table 12).
Table 12. Mean patient-level axial cleft width according to cleft laterality.
| Cleft Laterality | n | Mean ± SD (mm) |
|---|---|---|
| Unilateral left | 14 | 5.51 ± 3.18 |
| Unilateral right | 7 | 5.59 ± 1.32 |
| Bilateral | 12 | 7.15 ± 2.65 |
3.3.1. Intra-Examiner Reliability
Intra-examiner reliability was high for both axial cleft-width and corrected-coronal depth measurements.
For right-sided axial width measurements, the ICC was 0.942 (95% CI, 0.82–0.98; n = 13). For right-sided corrected-coronal depth, the ICC was 0.994 (95% CI, 0.98–1.00; n = 12).
For left-sided axial width, the ICC was 0.970 (95% CI, 0.89–0.99; n = 11), while the ICC for left-sided corrected-coronal depth was 0.976 (95% CI, 0.91–0.99; n = 10).
Across the paired measurements, the overall ICC was 0.974 (95% CI, 0.95–0.99). The mean signed difference between repeated measurements was 0.11 mm, with 95% limits of agreement from −0.84 to 1.06 mm.
Categorical reliability was assessed via a blinded re-read of all 33 cases, performed after an interval sufficient to minimize recall. Cohen’s kappa was 0.86 for nasopalatine canal position and 0.88 for nasal septal deviation, both indicating almost-perfect agreement (Landis and Koch benchmarks); paired repeat readings were not available for canine or lateral incisor status in this dataset.
These results indicate high intra-examiner agreement for the linear cleft measurements.
3.3.2. Cleft Width According to Sex and Adjacent Anatomical Findings
Mean axial cleft width was 5.94 ± 3.18 mm among females and 6.29 ± 2.28 mm among males (Mann–Whitney U = 114.5, p = 0.449).
Mean corrected-coronal depth was 7.72 ± 5.98 mm among females and 7.56 ± 3.27 mm among males (Mann–Whitney U = 116.5, p = 0.494).
Axial cleft width differed according to nasopalatine canal position (Kruskal–Wallis H = 7.44, p = 0.024). Mean axial width was 7.82 ± 2.79 mm when the canal was centered, 4.87 ± 2.37 mm when the canal deviated to the right, and 5.93 ± 2.28 mm when it deviated to the left.
Corrected-coronal depth did not differ significantly according to nasopalatine canal position (H = 2.39, p = 0.302).
Neither axial cleft width nor corrected-coronal depth differed significantly according to nasal septal deviation (H = 0.13, p = 0.721 and H = 0.05, p = 0.827, respectively) (Table 13).
Table 13. Cleft width and corrected-coronal depth correlated with sex and with the position of adjacent midline structures.
| Comparison | Test | Statistic | p -Value |
|---|---|---|---|
| Axial width vs. sex | Mann–Whitney U | U = 114.5 | 0.449 |
| Axial width vs. nasopalatine canal position (3 groups) | Kruskal–Wallis | H = 7.44 | 0.024 |
| Axial width vs. nasal septal deviation | Kruskal–Wallis | H = 0.13 | 0.721 |
| Corrected-coronal depth vs. sex | Mann–Whitney U | U = 116.5 | 0.494 |
| Corrected-coronal depth vs. nasopalatine canal position (3 groups) | Kruskal–Wallis | H = 2.39 | 0.302 |
| Corrected-coronal depth vs. nasal septal deviation | Kruskal–Wallis | H = 0.05 | 0.827 |
3.4. Objective 3: Nasopalatine Canal Position and Nasal Septal Deviation
Overall, the nasopalatine canal was positioned toward the right in 14 patients (42.4%), centered in 11 patients (33.3%), and toward the left in 8 patients (24.2%). Of the 11 centrally classified canals, 9 were centered on both the primary and blinded repeat reading (confirmed midline) and 2 were reclassified as laterally deviated on repeat reading (indeterminate rather than truly centered); all 11 were retained within the centered category for the primary analysis (Section 4).
The nasal septum deviated toward the left in 21 patients (63.6%), toward the right in 11 patients (33.3%), and showed no appreciable deviation in 1 patient (3.0%) (Table 14).
Table 14. Overall prevalence of nasopalatine canal position and nasal septal deviation ( n = 33).
| Finding | n | % |
|---|---|---|
| Nasopalatine canal—right | 14 | 42.4 |
| Nasopalatine canal—center | 11 | 33.3 |
| Nasopalatine canal—left | 8 | 24.2 |
| Nasal septum—left | 21 | 63.6 |
| Nasal septum—right | 11 | 33.3 |
| Nasal septum—no deviation | 1 | 3.0 |
Nasopalatine canal position was significantly associated with cleft laterality. The Pearson chi-square statistic was χ2 = 15.94 with 4 degrees of freedom (p = 0.003), while the Fisher–Freeman–Halton exact test yielded p = 0.002 (Table 15).
Table 15. Nasopalatine canal position according to cleft laterality.
| Cleft Laterality | Canal Right | Canal Center | Canal Left | Total |
|---|---|---|---|---|
| Unilateral left | 9 | 5 | 0 | 14 |
| Unilateral right | 2 | 0 | 5 | 7 |
| Bilateral | 3 | 6 | 3 | 12 |
Nasal septal deviation was also significantly associated with cleft laterality. The Pearson chi-square statistic was χ2 = 15.00 with 4 degrees of freedom (p = 0.005), while the Fisher–Freeman–Halton exact test yielded p = 0.001 (Table 16).
Table 16. Nasal septal deviation according to cleft laterality.
| Cleft Laterality | Septum Left | Septum Right | No Deviation | Total |
|---|---|---|---|---|
| Unilateral left | 13 | 1 | 0 | 14 |
| Unilateral right | 1 | 6 | 0 | 7 |
| Bilateral | 7 | 4 | 1 | 12 |
Among the 21 unilateral cases, 16 had a clearly directional nasopalatine canal position after excluding centrally positioned canals. The canal was positioned on the side opposite the cleft in 14 of these 16 cases (87.5%) and on the same side in 2 cases (12.5%).
Nasal septal deviation was toward the same side as the cleft in 19 of the 21 unilateral cases (90.5%) and toward the opposite side in 2 cases (9.5%).
3.5. Sensitivity Analysis by Age
Because six patients were 7–8 years old, a sensitivity analysis was performed after excluding these younger patients. The resulting subgroup comprised 27 patients aged 9–23 years.
The association between lateral incisor status and canine eruption status remained non-significant in the older subgroup. The age difference between patients with an unerupted canine and those with both canines erupted remained significant, with mean ages of approximately 11.9 and 15.7 years, respectively (Mann–Whitney U = 37.0, p = 0.010).
Root resorption was observed in 3 of 31 present lateral incisors (9.7%) in the older subgroup, compared with 5 of 38 (13.2%) in the full dataset.
The associations between cleft laterality and nasopalatine canal position and between cleft laterality and nasal septal deviation also remained statistically significant in the older subgroup (exact p = 0.005 and p = 0.004, respectively).
Overall, exclusion of the youngest patients did not materially alter the direction of the principal findings. Figure 5 summarizes these primary comparisons by cleft laterality: the two significant, reciprocal findings for nasopalatine canal position (A) and nasal septal deviation (B), the significant association between age and canine eruption status (C), and the non-significant cleft-width comparison (D) shown for context.
[图:Primary outcome comparisons by cleft laterality. ( A ) Nasopalatine canal position differed significantly by cleft later]

4. Discussion
This retrospective CBCT analysis of 33 patients with cleft palate examined the relationship between maxillary canine and lateral incisor status, the two-dimensional dimensions of the alveolar cleft, and the position of two adjacent midline structures—the nasopalatine canal and the nasal septum—in relation to cleft laterality, age, and sex. The distribution of cleft laterality in this cohort (left-sided in 42.4%, bilateral in 36.4%, right-sided in 21.2%) is broadly consistent with the wider epidemiological literature on cleft palate, in which left-sided unilateral involvement is consistently reported as the most common presentation, even as birth prevalence and phenotypic distribution vary by population [1,2,3,4].
The prevalence of lateral incisor absence observed here—45.5% of patients missing at least one lateral incisor, and 39.4% missing both—sits within the range reported in larger cleft cohorts using comparable tooth-agenesis classification systems. Using the Tooth Agenesis Code, López-Giménez et al. [10] reported agenesis in approximately 51% of unilateral and bilateral cleft lip and palate patients, with the lateral incisor the tooth most frequently affected, while Bartzela et al. [11] found agenesis in nearly half of a Dutch unilateral cleft cohort, with the cleft-side lateral incisor absent in roughly two of five patients, and Haque and Alam [12] identified missing maxillary lateral incisors as the single most consistent dental anomaly across cleft severities and populations. The present findings therefore corroborate this literature rather than diverging from it, reinforcing that lateral incisor absence—whether reflecting true congenital agenesis or non-visualization at the time of imaging (Section 2.5)—should be anticipated in close to half of cleft palate patients regardless of the specific population studied. Canine status in this cohort was weighted toward the unerupted category (60.6% right, 54.5% left; one left canine, 3.0%, was congenitally absent), consistent with the broader recognition that eruption of the maxillary canine adjacent to an alveolar cleft is frequently disrupted [25]. Critically, however, canine status was not significantly associated with lateral incisor status in this sample, whether tested per side (right side p = 1.000; left side p = 0.733); because the two sides of an individual patient are not independent observations, no inferential test was performed on the pooled tooth-side data (Section 3.2). This null finding is concordant with Oberoi et al. [9], who, using three-dimensional CBCT assessment of the canine eruption pathway in bone-grafted alveolar clefts, likewise found no significant association between congenital absence of the lateral incisor and canine eruption failure; together, the two studies suggest that canine eruption disturbance in cleft patients may be driven predominantly by the alveolar bony defect itself and the timing of bone grafting, rather than by the presence or absence of the adjacent lateral incisor. This contrasts with the general orthodontic literature outside the cleft population, where the initial three-dimensional position of an impacted canine—angulation, vertical displacement, mesial sector position—has been shown to be the dominant prognostic factor for eruption success [15], again pointing to canine position itself, rather than neighboring tooth status, as the more clinically actionable variable.
Apical root resorption was identified in 13.2% of lateral incisors classified as present, a figure lower than resorption rates sometimes reported in general (non-cleft) populations with impacted canines, where thinner labial alveolar bone and more labially inclined lateral incisor roots have been shown to substantially increase resorption risk [14], and where canine angulation and degree of radiographic overlap are established risk factors [13]. Because the present study did not measure alveolar bone thickness or root inclination, a direct mechanistic comparison with these bone-thickness-driven models is not possible; the comparatively lower resorption prevalence observed here may in part reflect the relatively young age of several cases (18.2% imaged at 7–8 years, before root maturity is reliably complete), which would tend to under-detect resorption that develops later as the canine continues its eruptive path. Consistent with this developmental interpretation, patient age was not significantly associated with lateral incisor status (p = 0.703) or root resorption (p = 0.414), but was significantly associated with canine status (p = 0.005): younger patients were substantially more likely to present with an unerupted canine (mean age 10.8 years) than an erupted one (mean age 15.1 years), while sex showed no such association (p = 1.000). This age effect is best explained by normal physiological eruption timing—the maxillary canine typically erupts between 7 and 11 years of age [5]—rather than a cleft-specific pathological process, and underscores the importance of age-stratified interpretation when canine eruption status is used as an outcome measure in cleft research. Neither cleft laterality nor the specific side affected by the cleft was significantly associated with lateral incisor status, root resorption, or canine status in this sample (all p > 0.14), suggesting that at the sample size available here, these dentoalveolar anomalies behave more as a generalized feature of the cleft phenotype than as a strictly lateralized, mechanically localized effect.
Turning from the dentition to the dimensions of the cleft itself, mean axial cleft width in this cohort (6.29 ± 2.72 mm pooled across sides) is broadly comparable in order of magnitude to alveolar cleft dimensions reported in other CBCT-based cohorts using three-dimensional or multi-planar measurement protocols, which have consistently favored volumetric or multi-plane assessment over single linear measurements for capturing the true extent of the defect [6,7]. Cleft width did not differ significantly across left-sided, right-sided, and bilateral cleft groups (Kruskal–Wallis p = 0.150), nor between unilateral and bilateral cleft considered as a simplified two-group comparison (p = 0.072), although bilateral clefts were numerically the widest of the three groups (7.15 mm vs. 5.51–5.59 mm for left and right unilateral clefts, respectively); nor was cleft width significantly associated with age (Spearman’s rho = 0.158, p = 0.378) or sex (p = 0.449). The non-significant bilateral-wider trend is directionally consistent with volumetric evidence from Regnstrand, Bousiou et al. (2025) [8], who used three-dimensional CBCT to show that bilateral alveolar clefts behave as two only partly independent defects with unequal bone-graft fill between the first- and second-grafted sides (47% vs. 33%), implying that bilateral clefts are architecturally more complex than unilateral clefts even when overall linear width is similar; the absence of statistical significance in the present comparison is most plausibly attributable to sample size (12 bilateral and 21 unilateral patients) rather than a true absence of an underlying difference, and should be revisited once cleft width data collection is complete for the full cohort. One further, unexpected association emerged when cleft width was tested against nasopalatine canal position: axial width differed significantly across the three canal-position groups (Kruskal–Wallis H = 7.44, p = 0.024), with a centrally positioned canal associated with the widest clefts. This should be interpreted cautiously, however, since a centrally positioned canal was itself more common in bilateral cleft cases (50.0%) than in unilateral cleft (35.7% left-sided, 0.0% right-sided), and bilateral clefts were independently the widest laterality group; the width–canal-position association therefore most plausibly reflects this shared relationship with bilaterality rather than an independent mechanistic link between cleft size and canal position. No comparable prior study in the reviewed literature appears to have directly tested the correlation between cleft width and nasopalatine canal or nasal septal position, so this association—and its likely confounding by laterality—is presented here as a preliminary, hypothesis-generating observation rather than an established finding, and coronal depth showed no corresponding association with either structure (both p > 0.30).
The strongest and most consistent findings in this study concerned the two midline structures adjacent to the cleft. Both the nasopalatine canal and the nasal septum showed a statistically significant relationship with cleft laterality (exact Fisher–Freeman–Halton p = 0.002 and p = 0.001, respectively), and the two structures deviated in reciprocal directions relative to the cleft side: among unilateral cases, the nasopalatine canal deviated away from the cleft side in 87.5% of assessable cases, while the nasal septum deviated toward the cleft side in 90.5% of cases. The magnitude and direction of the septal finding align closely with Vicente, Wiedel et al. [19], who reported the nasal septum curved toward the cleft or graft side in 87% of unilateral cases using a comparable CBCT-based evaluation of cleft volume and adjacent anatomical structures—a striking convergence between two independent cohorts. Other CBCT-based investigations have similarly established that nasal septal deviation is significantly more pronounced in cleft lip and palate patients than in non-cleft or skeletal Class III controls [22], and that the degree of deviation correlates with cleft severity [21], lending further support to the present finding that septal position is systematically tied to the underlying cleft anatomy rather than incidental. It is worth noting that earlier work using direct visual scoring reported the cartilaginous nasal tip and anterior nasal spine deviating toward the non-cleft side [20]—apparently the opposite direction to the septal body deviation observed here and by Vicente, Wiedel et al. [19]. Rather than a genuine contradiction, this most likely reflects that the nasal tip, anterior nasal spine, and posterior/mid-septal body are anatomically distinct landmarks that can deviate along different, even opposing, trajectories within a single S- or C-shaped deformity, as is well recognized in cleft rhinoseptal anatomy; the present study measured septal position at the level of the nasal floor on axial and coronal CBCT, which is not directly equivalent to nasal tip or anterior nasal spine position on clinical or photographic assessment. The nasopalatine canal findings extend previous CBCT-based work demonstrating that canal morphology itself—not only its position—is altered in cleft patients, with funnel-, banana-, and needle-shaped canals, a larger foramen and canal diameter, and a shorter overall canal length all reported significantly more frequently in cleft than non-cleft controls [18]; the present study adds a laterality-specific dimension to this picture, showing that the canal’s position within the anterior maxilla is systematically displaced away from the cleft side in unilateral cases. Combined with the reciprocal septal finding, this pattern is consistent with the alveolar and palatal bony defect exerting an asymmetric influence on the entire anterior nasal floor complex, displacing the septum toward the defect while the bony canal is displaced away from it, rather than the two structures being affected independently. From a clinical standpoint, this reciprocal relationship may be of practical value in presurgical CBCT planning in at least three concrete ways. First, when planning the surgical approach and graft harvest trajectory for secondary alveolar bone grafting, awareness that the nasopalatine canal is statistically more likely to lie toward the non-cleft side in unilateral cases can help the surgeon anticipate its position on the preoperative scan and avoid inadvertent canal violation during graft-bed preparation, particularly in cases where the canal is difficult to trace directly, an application directly relevant to the surgical planning literature on secondary alveolar bone grafting [8,26]. Second, if future implant-based rehabilitation of the anterior maxilla is anticipated once the patient reaches skeletal maturity, the same laterality-dependent canal position could inform where implant osteotomies are more or less likely to encroach on the canal, complementing existing morphometric data on canal shape and diameter in cleft patients [18]. Third, the systematic septal deviation toward the cleft side is a reminder to orthodontists and rhinologists coordinating presurgical orthopedics or septorhinoplasty timing that nasal airway assessment should routinely accompany dento-alveolar planning in this population, since the two structures appear to be displaced by a shared mechanism rather than varying independently. These are proposed clinical applications rather than tested interventions, and each would need to be evaluated prospectively—for example, by comparing planned versus actual canal position on intraoperative navigation, or by correlating septal deviation with subjective nasal airway outcomes—before being adopted as formal planning guidance.
Beyond these procedural applications, the systematic and reciprocal relationship observed here between cleft laterality and the position of two independent midline structures carries a broader interpretive implication. If cleft lip and palate were purely a localized failure of alveolar and palatal fusion, there is no obvious mechanical reason why the nasopalatine canal and nasal septum—structures that lie outside the cleft margin itself—should shift in a laterality-dependent, reciprocal pattern. That they do so—consistently across this cohort and convergent with an independent cohort [19]—suggests cleft lip and palate disturbs the anterior nasomaxillary complex as a whole, not just the alveolar segment. This interpretation is reinforced by several recent CBCT studies reporting nasal septal, nasal complex, and maxillary sinus asymmetry in cleft cohorts [27,28,29,30], although, as in the present study, these structures have generally been examined individually rather than alongside the dentoalveolar cleft itself. Recent CBCT and digital-model evidence on the dentoalveolar side of this picture points the same way: agenesis patterns continue to be reported by cleft laterality [31], and canine-substitution approaches for the agenesis space remain an active area of study [32], reinforcing that both the dentoalveolar and midline findings in cleft lip and palate warrant continued, laterality-specific characterization. This does not make the alveolar cleft any less clinically important, but it is a reason for CBCT protocols in cleft care to routinely capture the nasopalatine canal and nasal septum alongside the cleft itself—both as a diagnostic habit, and as a further test of this model in larger cohorts.
Study Limitations
This study has several limitations. First, the sample size was relatively small (n = 33), with particularly small subgroups for unilateral right-sided (n = 7) and bilateral (n = 12) clefts. Therefore, the study may have had limited power to detect modest associations, and non-significant findings should not be interpreted as evidence that no association exists. Several secondary analyses were exploratory, and no adjustment for multiple comparisons was performed.
Second, the retrospective single-center design limits generalizability. CBCT examinations were acquired for clinical purposes using non-uniform imaging protocols, including variation in field of view and CBCT unit, rather than under a standardized research protocol.
Third, although cleft measurements were largely complete, one anatomically eligible side could not be measured because of insufficient dental development to identify reliable measurement landmarks. In addition, one erroneous measurement recorded for a non-cleft side was identified during data verification and excluded from analysis. These issues were limited to individual measurements and did not alter the reported results.
Fourth, the cohort included patients aged 7–23 years, with six patients aged 7–8 years. Variation in dental developmental stage may affect interpretation of root resorption, lateral incisor development, and canine eruption. The sensitivity analysis excluding these younger patients showed that the principal findings, including the associations between cleft laterality and nasopalatine canal position and nasal septal deviation, remained statistically significant; however, the small sample limits the ability to exclude subtler age-related effects.
Fifth, all image assessments were performed by a single examiner. Intra-examiner reliability for the linear cleft measurements was excellent (pooled ICC(A,1) = 0.974; 95% CI, 0.95–0.99). For the two categorical variables underlying the principal significant findings of this study—nasopalatine canal position and nasal septal deviation—intra-examiner reliability was assessed via a blinded re-read of all 33 cases performed after an interval sufficient to minimize recall, with agreement quantified using Cohen’s kappa: κ = 0.86 for canal position and κ = 0.88 for septal deviation, both indicating almost-perfect agreement. Repeat categorical readings were not available for canine or lateral incisor status in this retrospective dataset, so their reliability could not be similarly quantified; this remains noted as a residual limitation.
Sixth, two aspects of midline-structure classification warrant caution. The anatomical midline used for both nasopalatine canal position and nasal septal deviation was defined from the midpoint of the nasal septum itself (Section 2.4); this is not circular for the canal, an independent structure, but it means septal position describes the septum’s course relative to this study’s own reference rather than displacement from a wholly independent skeletal axis. Separately, canal cases in which position could not be confidently lateralized were classified as centered together with cases in which the canal was genuinely at the midline (Section 2.5). Using agreement between the primary and blinded repeat reading (Section 2.6) as an operational criterion, 9 of the 11 canals classified as centered were centered on both readings (confirmed midline), while the remaining 2 were reclassified as laterally deviated on repeat reading (indeterminate rather than truly centered; Section 3.4). An independently defined skeletal landmark and a prospectively applied three-way centered/indeterminate/lateralized classification would further strengthen this distinction in future work.
A related direction for future work, beyond the scope of the present analysis, would be to evaluate maxillary sinus mucosal thickening in this population—its severity, and whether it extends to one or multiple paranasal sinuses—as an additional adjacent midfacial finding potentially associated with cleft laterality.
Seventh, classifying canines as erupted or unerupted does not distinguish physiological developmental non-eruption from pathological impaction. This distinction is particularly relevant in younger patients and would require longitudinal clinical information or standardized developmental criteria, which were unavailable in this retrospective dataset.
Despite these limitations, the study provides reproducible CBCT measurements and identifies significant associations between cleft laterality and the positions of the nasopalatine canal and nasal septum. These findings warrant confirmation in larger, multicenter studies using standardized imaging protocols and longitudinal assessment.
5. Conclusions
This retrospective CBCT study found no significant association between cleft laterality and dentoalveolar status—lateral incisor presence, root resorption, canine eruption, or cleft width—beyond the expected relationship between canine eruption and age; given the modest sample size, these findings should be regarded as inconclusive rather than as evidence of no true association. By contrast, both nasopalatine canal position and nasal septal deviation were significantly and reciprocally associated with cleft laterality. Because these two structures are anatomically distinct from the alveolar cleft itself, this dissociation supports characterizing cleft lip and palate as a regional craniofacial disturbance of the anterior nasomaxillary complex rather than an isolated alveolar defect, with potential relevance for pre-surgical CBCT planning. These findings warrant confirmation in larger, multicenter studies using standardized imaging protocols.
Acknowledgments
The authors gratefully acknowledge the Deanship of Scientific Research (DSR) at King Abdulaziz University, Jeddah, Saudi Arabia, for funding this project under grant No. (IPP: 976-165-2026) and for providing technical support. Also, the author thanks the Oral Radiology Department, King Abdulaziz University Dental Hospital (KAUDH), Jeddah, Saudi Arabia, for providing access to the archived CBCT examinations and imaging facilities that made this study possible. During the preparation of this manuscript/study, the author used Claude (Claude Sonnet 5, Anthropic) for literature search support, statistical cross-checking, and language editing assistance. The authors have reviewed and edited the output and take full responsibility for the content of this publication.
Abbreviations
The following abbreviations are used in this manuscript: CBCT, cone beam computed tomography; ICC, intraclass correlation coefficient; IPDTOC, International Perinatal Database of Typical Oral Clefts; KAUDH, King Abdulaziz University Dental Hospital; MPR, multiplanar reconstruction; WHO, World Health Organization.
Supplementary Materials
The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/diagnostics16193140/s1. File S1: STROBE Checklist for Cross-Sectional Studies.
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Institutional Review Board Statement
The study was conducted in accordance with the Declaration of Helsinki and approved by the Research Ethics Committee, Faculty of Dentistry, King Abdulaziz University, Jeddah, Saudi Arabia (protocol code 120-05-26, approved 25 June 2026).
Informed Consent Statement
Patient consent was waived by the Research Ethics Committee, Faculty of Dentistry, King Abdulaziz University, because the study involved retrospective analysis of de-identified, archived CBCT examinations, was classified as posing no human risk, and individual re-contact was not feasible.
Data Availability Statement
The data presented in this study are available on request from the corresponding author due to institutional and patient-privacy restrictions on the retrospective clinical imaging archive.
Conflicts of Interest
The author declares no conflicts of interest.
Funding Statement
The authors gratefully acknowledge the Deanship of Scientific Research (DSR) at King Abdulaziz University, Jeddah, Saudi Arabia, for funding this project under grant No. (IPP: 976-165-2026) and for providing technical support.
Footnotes
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References
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Associated Data
Supplementary Materials
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Data Availability Statement
The data presented in this study are available on request from the corresponding author due to institutional and patient-privacy restrictions on the retrospective clinical imaging archive.
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