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非综合征型唇裂伴或不伴腭裂全基因组关联研究数据中显性和隐性遗传模型的研究。

Investigation of dominant and recessive inheritance models in genome-wide association studies data of nonsyndromic cleft lip with or without cleft palate.

机构信息

Institute of Human Genetics, University of Bonn, Bonn, Germany.

Department of Genomics, Life & Brain Center, University of Bonn, Bonn, Germany.

出版信息

Birth Defects Res. 2018 Mar 1;110(4):336-341. doi: 10.1002/bdr2.1144. Epub 2017 Nov 14.

Abstract

Nonsyndromic cleft lip with or without cleft palate (nsCL/P) is one of the most common congenital malformation worldwide, and its etiology involves both genetic and environmental factors. Recent genome-wide and targeted genetic studies of nsCL/P have identified numerous genetic risk loci, under the hypothesis of a multiplicative mode of inheritance. The present study investigated whether novel nsCL/P risk loci could be identified by analyzing dominant/recessive genetic effects in single nucleotide polymorphism (SNP) data from genome-wide association studies. For this purpose, a genome-wide investigation of dominant/recessive common SNP effects was performed in our previously published meta-analysis data set. Twenty-four loci were identified as candidate regions. In a subsequent association analysis in an independent study cohort of 224 nsCL/P patients and 986 controls of European descent, none of the loci could be replicated. Therefore, our strategy of identifying novel loci by applying different genetic models did not yield any novel findings, suggesting that recessive/dominant common variation only make a limited contribution to nsCL/P in Europeans. However, we cannot rule out that such effects are present at some of the loci that have previously been identified, or are present in different populations.

摘要

非综合征性唇裂伴或不伴腭裂(nsCL/P)是全球最常见的先天性畸形之一,其病因涉及遗传和环境因素。最近对 nsCL/P 的全基因组和靶向遗传研究,在多效遗传模式的假设下,确定了许多遗传风险位点。本研究通过分析全基因组关联研究中 SNP 数据的显性/隐性遗传效应,探讨是否可以鉴定出新型 nsCL/P 风险位点。为此,在我们之前发表的荟萃分析数据集中,对显性/隐性常见 SNP 效应进行了全基因组研究。鉴定出 24 个候选区域。在随后对 224 例 nsCL/P 患者和 986 例欧洲血统对照的独立研究队列进行的关联分析中,没有一个位点可以被复制。因此,我们通过应用不同遗传模型来鉴定新型位点的策略没有产生任何新的发现,这表明隐性/显性常见变异对欧洲人的 nsCL/P 仅有有限的贡献。然而,我们不能排除之前已经确定的某些位点或在不同人群中存在这种影响。

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