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对日本人群子宫内膜异位症遗传易感性的全基因组关联扫描的荟萃分析。

Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population.

机构信息

Department of Obstetrics and Gynecology, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Niigata, Japan.

出版信息

J Hum Genet. 2010 Dec;55(12):816-21. doi: 10.1038/jhg.2010.118. Epub 2010 Sep 16.

Abstract

To identify susceptibility genes for endometriosis in Japanese women, genome-wide association (GWA) analysis was performed using two case-control cohorts genotyped with the Affymetrix Mapping 500K Array or Genome-Wide Human SNP Array 6.0. In each of the two array cohorts, stringent quality control (QC) filters were applied to newly obtained genotype data, together with previously analyzed data from the Japanese Integrated Database Project. After QC-based filtering of samples and single nucleotide polymorphisms (SNPs) in each cohort, 282 838 SNPs in both genotyping platforms were tested for association with endometriosis using a meta-analysis of the two GWA studies with 696 patients with endometriosis and 825 controls. The meta-analysis revealed that a common susceptibility locus conferring a large effect on the disease risk was unlikely. On the other hand, an excess of SNPs with P-values <10(-4) (36 vs 28 SNPs expected by chance) was observed in the meta-analysis. Of note, four of the top five SNPs with P-values <10(-5) were located in and around IL1A (interleukin 1α), which might be a functional candidate gene for endometriosis. Further studies with larger case-control cohorts will be necessary to elucidate the genetic risk factors.

摘要

为了鉴定日本女性子宫内膜异位症的易感基因,对两个经 Affymetrix Mapping 500K 阵列或 Genome-Wide Human SNP Array 6.0 基因分型的病例对照队列进行了全基因组关联(GWA)分析。在两个阵列队列中,都应用了严格的质量控制(QC)过滤器来处理新获得的基因型数据,以及日本综合数据库项目中以前分析的数据。在对每个队列中的样本和单核苷酸多态性(SNP)进行基于 QC 的过滤后,使用对 696 名子宫内膜异位症患者和 825 名对照进行的两项 GWA 研究的荟萃分析,对两种基因分型平台中的 282838 个 SNP 与子宫内膜异位症的相关性进行了检测。荟萃分析显示,不太可能存在赋予疾病风险大影响的常见易感位点。另一方面,在荟萃分析中观察到,具有 P 值<10(-4)的 SNP 数量过多(预期的机会为 28 个 SNP,实际有 36 个)。值得注意的是,P 值<10(-5)的前五个 SNP 中有四个位于 IL1A(白细胞介素 1α)内或周围,这可能是子宫内膜异位症的功能候选基因。需要进一步开展更大规模的病例对照队列研究,以阐明遗传风险因素。

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