Family-based study of association between ENPP1 genetic variants and craniofacial morphology

Abstract

Background: Human craniofacial morphology is characterized by considerable diversity among individuals. The ENPP1 gene is essential for bone physiology. However, the potential effects of its genetic variants on head size phenotypes have not yet been studied.

Aim: The aim of this research was to investigate the association of polymorphisms in the ENPP1 locus with normal variability of craniofacial phenotypes.

Subjects and methods: Fourteen SNPs and 13 haplotypes in the ENPP1 locus were tested for association with six head size traits in 1042 Western Eurasian individuals.

Results: The most significant and consistent association was observed between upper facial height and the polymorphisms located near the promoter region and upstream from ENPP1 gene (p = 0.00009), which remained significant after adjustment for multiple testing. Additionally, association signals were detected between head breadths and lower face height, and markers residing in or close to the promoter and 3^′ untranslated regions of the ENPP1 gene (p < 0.05).

Conclusions: The findings obtained in this study suggest that the upstream, promoter and 3^′ untranslated regions in the ENPP1 locus harbor genetic variants affecting different aspects of craniofacial morphology. Further research is required to validate the relevancy of the potentially functional ENPP1 regions to normal and pathologic craniofacial growth.

Keywords::

• Genetic
• FBAT
• SNPs
• head
• normal variability

Declaration of interest: This study was funded by a grant from the Recanati Foundation 2008 to GL. The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.