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非综合征性唇腭裂多态性影响正常唇部形态。

Non-syndromic Cleft Lip and Palate Polymorphisms Affect Normal Lip Morphology.

作者信息

Wilson-Nagrani Caryl, Richmond Stephen, Paternoster Lavinia

机构信息

Department of Orthodontics, University Dental Hospital, Cardiff, United Kingdom.

MRC Integrative Epidemiology Unit, School of Social and Community Medicine, University of Bristol, Bristol, United Kingdom.

出版信息

Front Genet. 2018 Oct 24;9:413. doi: 10.3389/fgene.2018.00413. eCollection 2018.

Abstract

Non-syndromic cleft lip with or without palate (NSCL/P) is a frequent malformation of the facial region. Genetic variants (SNPs) within nineteen loci have been previously associated with NSCL/P in GWAS studies of European individuals. These common variant SNPs may have subtler effects on the morphology of the lip and face in unaffected individuals. Several studies have investigated the genetic influences on facial morphology using land-marking methods, but these landmarks are sparse in the lip region. The aim of this study is to assess for associations between the nineteen NSCL/P SNPs and normal lip phenotypes, using a detailed categorical scale. Three-dimensional laser scanned facial images were obtained of 4,747 subjects recruited from the Avon Longitudinal Study of Parents and Children (ALSPAC) and genetic data was available for 3,643 of them. A polygenetic risk score (PRS) combining the nineteen NSCL/P SNPs was associated with V-shaped Cupid's bow ( = 3 × 10) and narrow philtrum ( = 2 × 10) phenotypes. Analysis of individual SNPs found strong evidence for association between rs227731 and skeletal II pattern ( = 5 × 10). This study finds that known NSCL/P SNPs affect lip phenotypes in the general population, and an increased PRS is associated with narrow philtrum and V-shaped Cupid's bow. However, the difference in NSCL/P PRS between people with and without certain lip features is unlikely to be great enough to serve as a useful marker of NSCL/P risk.

摘要

非综合征性唇裂伴或不伴腭裂(NSCL/P)是面部常见的畸形。在欧洲人群的全基因组关联研究(GWAS)中,19个基因座内的遗传变异(单核苷酸多态性,SNPs)先前已与NSCL/P相关联。这些常见的变异SNPs可能对未受影响个体的嘴唇和面部形态有更细微的影响。几项研究使用地标法研究了遗传对面部形态的影响,但这些地标在唇部区域很稀疏。本研究的目的是使用详细的分类量表评估19个NSCL/P SNPs与正常唇部表型之间的关联。从阿冯父母与儿童纵向研究(ALSPAC)招募的4747名受试者获得了三维激光扫描面部图像,其中3643人有基因数据。结合19个NSCL/P SNPs的多基因风险评分(PRS)与V形丘比特弓( = 3 × 10)和窄人中( = 2 × 10)表型相关。对单个SNPs的分析发现rs227731与骨骼II型模式之间存在关联的有力证据( = 5 × 10)。本研究发现,已知的NSCL/P SNPs会影响一般人群的唇部表型,PRS增加与窄人中及V形丘比特弓相关。然而,有或没有某些唇部特征的人之间NSCL/P PRS的差异不太可能大到足以作为NSCL/P风险的有用标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2225/6207999/fa9d9880c8dd/fgene-09-00413-g0001.jpg

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