AUTHOR=Indencleef Karlijne , Roosenboom Jasmien , Hoskens Hanne , White Julie D. , Shriver Mark D. , Richmond Stephen , Peeters Hilde , Feingold Eleanor , Marazita Mary L. , Shaffer John R. , Weinberg Seth M. , Hens Greet , Claes Peter 

TITLE=Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation

JOURNAL=Frontiers in Genetics

VOLUME=9

YEAR=2018

URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2018.00502

DOI=10.3389/fgene.2018.00502

ISSN=1664-8021

ABSTRACT=<p><bold>Objectives:</bold> Orofacial clefting is one of the most prevalent craniofacial malformations. Previous research has demonstrated that unaffected relatives of patients with non-syndromic cleft lip with/without cleft palate (NSCL/P) show distinctive facial features, which can be an expression of underlying NSCL/P susceptibility genes. These results support the hypothesis that genes involved in the occurrence of a cleft also play a role in normal craniofacial development. In this study, we investigated the influence of genetic variants associated with NSCL/P on normal-range variation in facial shape.</p><p><bold>Methods:</bold> A literature review of genome wide association studies (GWAS) investigating the genetic etiology of NSCL/P was performed, resulting in a list of 75 single nucleotide polymorphisms (SNPs) located in 38 genetic loci. Genotype data were available for 65 of these selected SNPs in three datasets with a combined sample size of 7,418 participants of European ancestry, whose 3D facial images were also available. The effect of each SNP was tested using a multivariate canonical correlation analysis (CCA) against 63 hierarchically-constructed facial segments in each of the three datasets and meta-analyzed. This allowed for the investigation of associations between SNPs known to be involved in NSCL/P and normal-range facial shape variations in a global-to-local perspective, without preselecting specific facial shape features or characteristics.</p><p><bold>Results:</bold> Six NSCL/P SNPs showed significant associations with variation in normal-range facial morphology. rs6740960 showed significant effects in the chin area (<italic>p</italic> = 3.71 × 10<sup>−28</sup>). This SNP lies in a non-coding area. Another SNP, rs227731 near the <italic>NOG</italic> gene, showed a significant effect in the philtrum area (<italic>p</italic> = 1.96 × 10<sup>−16</sup>). Three SNPs showed significant effects on the shape of the nose. rs742071 (<italic>p</italic> = 8.71 × 10<sup>−14</sup>), rs34246903 (<italic>p</italic> = 6.87 × 10<sup>−12</sup>), and rs10512248 (<italic>p</italic> = 8.4 × 10<sup>−9</sup>). Respectively, these SNPs are annotated to <italic>PAX7, MSX1</italic>, and <italic>PTCH1</italic>. Finally, rs7590268, an intron variant of <italic>THADA</italic>, showed an effect in the shape of the supraorbital ridge (<italic>p</italic> = 3.84 × 10<sup>−7</sup>).</p><p><bold>Conclusions:</bold> This study provides additional evidence NSCL/P-associated genetic variants influence normal-range craniofacial morphology, with significant effects observed for the chin, the nose, the supraorbital ridges and the philtrum area.</p>