In this study we aimed to determine the effect of WNT10A variants on dental development in patients with oligodontia. Forty-three (25 boys and 18 girls) individuals were eligible for this study. Stage of development for each present tooth was assessed using the Demirjian method. In case no corresponding tooth was present, regression equations were applied for dental age to be calculated. The ratio between length of root and length of crown was ascertained for each present tooth in all quadrants. All patients were physically examined by a clinical geneticist and DNA analysis of the WNT10A gene was performed. Linear regression models were applied to analyze the association between WNT10A variants and dental age. The same analysis was applied to study the association between WNT10A variants and root elongation for each present tooth. One ordinal regression model was applied to analyze the association between WNT10A variants and development of present maxillary and mandibular teeth. Thirty-six (84%) patients were detected with WNT10A variants of which six patients displayed evident ectodermal features. Dental age was 1.50 (95% confidence interval (CI): -2.59, -0.42) to 1.96 (95% CI: -3.76, -0.17) years lower in patients with WNT10A variants compared with patients without variants. The development of maxillary canine, maxillary second molar and mandibular second molar was statistically significantly delayed in patients with WNT10A variants compared with patients without variants. The impact of WNT10A variants on dental development increases with presence of the nonsense c.(321C>A p.(C107∗)) variant and the number of missing teeth.

Additional Metadata
Persistent URL dx.doi.org/10.1038/ejhg.2016.117, hdl.handle.net/1765/96765
Journal European Journal of Human Genetics
Citation
Dhamo, B, Fennis, W. (Willem), Créton, M. (Marijn), Vučić, S, Cune, M. (Marco), Ploos van Amstel, H.K, … Ongkosuwito, E.M. (2016). The association between WNT10A variants and dental development in patients with isolated oligodontia. In European Journal of Human Genetics (Vol. 25, pp. 59–65). doi:10.1038/ejhg.2016.117