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Candidate genes for obesity-susceptibility show enriched association within a large genome-Wide association study for BMI

机译:肥胖易感性候选基因在大型BMI的全基因组关联研究中显示出丰富的关联

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摘要

Before the advent of genome-wide association studies (GWASs), hundreds of candidate genes for obesity-susceptibility had been identified through a variety of approaches. We examined whether those obesity candidate genes are enriched for associations with body mass index (BMI) compared with non-candidate genes by using data from a large-scale GWAS. A thorough literature search identified 547 candidate genes for obesity-susceptibility based on evidence from animal studies, Mendelian syndromes, linkage studies, genetic association studies and expression studies. Genomic regions were defined to include the genes ±10 kb of flanking sequence around candidate and non-candidate genes. We used summary statistics publicly available from the discovery stage of the genome-wide meta-analysis for BMI performed by the genetic investigation of anthropometric traits consortium in 123 564 individuals. Hypergeometric, rank tail-strength and gene-set enrichment analysis tests were used to test for the enrichment of association in candidate compared with non-candidate genes. The hypergeometric test of enrichment was not significant at the 5% P-value quantile (P = 0.35), but was nominally significant at the 25% quantile (P = 0.015). The rank tail-strength and gene-set enrichment tests were nominally significant for the full set of genes and borderline significant for the subset without SNPs at P 10 -7. Taken together, the observed evidence for enrichment suggests that the candidate gene approach retains some value. However, the degree of enrichment is small despite the extensive number of candidate genes and the large sample size. Studies that focus on candidate genes have only slightly increased chances of detecting associations, and are likely to miss many true effects in non-candidate genes, at least for obesity-related traits.
机译:在全基因组关联研究(GWAS)出现之前,已经通过多种方法鉴定了数百种肥胖易感性候选基因。我们通过使用来自大型GWAS的数据,检查了那些肥胖候选基因与非候选基因相比是否富含与体重指数(BMI)的关联。彻底的文献检索基于动物研究,孟德尔综合症,连锁研究,遗传关联研究和表达研究的证据,确定了547个肥胖易感性候选基因。基因组区域被定义为包括候选基因和非候选基因周围±10 kb侧翼序列的基因。我们使用了通过对123564名个体的人体测量学性状联盟进行基因调查而进行的BMI全基因组荟萃分析的发现阶段公开获得的摘要统计数据。与非候选基因相比,使用超几何,秩尾强度和基因集富集分析测试来测试候选者中联想的富集。富集的超几何检验在5%P值分位数(P = 0.35)时不显着,但在25%分位数(P = 0.015)时名义上显着。在P <10 -7时,秩尾强度和基因集富集测试对整个基因组具有名义上的显着性,而对于没有SNP的子集而言,边缘性显着。综上所述,观察到的富集证据表明候选基因方法保留了一定的价值。但是,尽管候选基因数量众多且样本量很大,但是富集程度却很小。专注于候选基因的研究发现关联的机会仅略有增加,并且可能会错过非候选基因的许多真实效应,至少对于肥胖相关性状而言。

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