Third molar agenesis in individuals with supernumerary teeth

IF 2.4 3区 医学 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Luca Friedli, Eva Henninger, Miltiadis A Makrygiannakis, Vasileios F Zymperdikas, Moschos A Papadopoulos, Georgios Kanavakis, Nikolaos Gkantidis
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Abstract

Objectives

To explore the association between third molar agenesis and supernumerary tooth formation in a white-European population.

Materials and Methods

A record review in various orthodontic clinics identified 380 eligible white-European individuals, half of whom had non-syndromic permanent supernumerary teeth (122 males and 68 females, totalling 244 supernumerary teeth; median age: 13.1, iqr: 1.5 years), and the other half were age- and sex-matched controls with full dentition, excluding the third molars. Tooth sequences were identified in panoramic radiographs.

Results

In the supernumerary group, approximately 80% of the individuals had a single supernumerary tooth, followed by those having two additional teeth. In both groups, there was no sexual dimorphism in third molar agenesis severity. The prevalence of third molar agenesis in the supernumerary group was similar to that of the control group (28/190 = 14.7% in both groups; p = 1.0). In total, 53 third molars were missing in the supernumerary group (n = 190) compared to 67 in the control group (n = 190; p = .862). The ratio of bilateral to unilateral third molar agenesis was significantly lower in the supernumerary group than in the control group (1.0 vs. 3.7, respectively; p = .026).

Conclusion

The presence of supernumerary teeth did not significantly alter the likelihood of third molar agenesis or its severity. Bilateral third molar agenesis was considerably less prevalent in individuals with supernumerary teeth compared to controls. The present novel findings have important clinical and developmental implications.

Abstract Image

超常牙齿患者的第三磨牙缺失。
目的探讨欧洲白人群体中第三磨牙缺失与超常牙形成之间的关联:通过对多家正畸诊所的记录进行审查,确定了 380 名符合条件的欧洲白人,其中一半人患有非综合征性恒牙外生齿(122 名男性和 68 名女性,共计 244 颗外生齿;中位年龄:13.1 岁,平均年龄:1.5 岁),另一半人在年龄和性别上与之匹配:中位年龄:13.1 岁,平均年龄:1.5 岁),另一半是年龄和性别匹配的对照组,他们拥有完整的牙齿,但不包括第三磨牙。在全景X光片上确定了牙齿序列:在超常牙组中,约 80% 的人有一颗超常牙,其次是有两颗额外牙齿的人。在这两组中,第三磨牙缺失的严重程度没有性别差异。超常牙组的第三磨牙缺失率与对照组相似(两组均为 28/190 = 14.7%;P = 1.0)。超常儿童组共有53颗第三磨牙缺失(n = 190),而对照组有67颗第三磨牙缺失(n = 190; p = .862)。双侧第三磨牙缺失与单侧第三磨牙缺失的比例在超常牙组明显低于对照组(分别为 1.0 与 3.7;P = .026):结论:超常牙的存在并不会明显改变第三磨牙缺失的可能性或其严重程度。与对照组相比,双侧第三磨牙缺失的发生率要低得多。这些新发现具有重要的临床和发育意义。
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来源期刊
Orthodontics & Craniofacial Research
Orthodontics & Craniofacial Research 医学-牙科与口腔外科
CiteScore
5.30
自引率
3.20%
发文量
65
审稿时长
>12 weeks
期刊介绍: Orthodontics & Craniofacial Research - Genes, Growth and Development is published to serve its readers as an international forum for the presentation and critical discussion of issues pertinent to the advancement of the specialty of orthodontics and the evidence-based knowledge of craniofacial growth and development. This forum is based on scientifically supported information, but also includes minority and conflicting opinions. The objective of the journal is to facilitate effective communication between the research community and practicing clinicians. Original papers of high scientific quality that report the findings of clinical trials, clinical epidemiology, and novel therapeutic or diagnostic approaches are appropriate submissions. Similarly, we welcome papers in genetics, developmental biology, syndromology, surgery, speech and hearing, and other biomedical disciplines related to clinical orthodontics and normal and abnormal craniofacial growth and development. In addition to original and basic research, the journal publishes concise reviews, case reports of substantial value, invited essays, letters, and announcements. The journal is published quarterly. The review of submitted papers will be coordinated by the editor and members of the editorial board. It is policy to review manuscripts within 3 to 4 weeks of receipt and to publish within 3 to 6 months of acceptance.
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