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A Replication Study of GWAS-Derived Lipid Genes in Asian Indians: The Chromosomal Region 11q23.3 Harbors Loci Contributing to Triglycerides

机译:GWAS衍生的脂质基因在亚洲印度人中的复制研究:染色体区域11q23.3港口基因贡献甘油三酸酯。

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摘要

Recent genome-wide association scans (GWAS) and meta-analysis studies on European populations have identified many genes previously implicated in lipid regulation. Validation of these loci on different global populations is important in determining their clinical relevance, particularly for development of novel drug targets for treating and preventing diabetic dyslipidemia and coronary artery disease (CAD). In an attempt to replicate GWAS findings on a non-European sample, we examined the role of six of these loci (CELSR2-PSRC1-SORT1 rs599839; CDKN2A-2B rs1333049; BUD13-ZNF259 rs964184; ZNF259 rs12286037; CETP rs3764261; APOE-C1-C4-C2 rs4420638) in our Asian Indian cohort from the Sikh Diabetes Study (SDS) comprising 3,781 individuals (2,902 from Punjab and 879 from the US). Two of the six SNPs examined showed convincing replication in these populations of Asian Indian origin. Our study confirmed a strong association of CETP rs3764261 with high-density lipoprotein cholesterol (HDL-C) (p = 2.03×10−26). Our results also showed significant associations of two GWAS SNPs (rs964184 and rs12286037) from BUD13-ZNF259 near the APOA5-A4-C3-A1 genes with triglyceride (TG) levels in this Asian Indian cohort (rs964184: p = 1.74×10−17; rs12286037: p = 1.58×10−2). We further explored 45 SNPs in a ∼195 kb region within the chromosomal region 11q23.3 (encompassing the BUD13-ZNF259, APOA5-A4-C3-A1, and SIK3 genes) in 8,530 Asian Indians from the London Life Sciences Population (LOLIPOP) (UK) and SDS cohorts. Five more SNPs revealed significant associations with TG in both cohorts individually as well as in a joint meta-analysis. However, the strongest signal for TG remained with BUD13-ZNF259 (rs964184: p = 1.06×10−39). Future targeted deep sequencing and functional studies should enhance our understanding of the clinical relevance of these genes in dyslipidemia and hypertriglyceridemia (HTG) and, consequently, diabetes and CAD.
机译:最近对欧洲人群进行的全基因组关联扫描(GWAS)和荟萃分析研究已经确定了许多以前与脂质调节有关的基因。在不同的全球人群中验证这些基因座对于确定其临床意义非常重要,尤其是对于开发用于治疗和预防糖尿病血脂异常和冠状动脉疾病(CAD)的新型药物靶标而言。为了在非欧洲样本上复制GWAS发现,我们检查了其中六个基因座的作用(CELSR2-PSRC1-SORT1 rs599839; CDKN2A-2B rs1333049; BUD13-ZNF259 rs964184; ZNF259 rs12286037; CETP rs3764261; APOE-C1来自锡克教糖尿病研究(SDS)的亚洲印度裔队列中的-C4-C2 rs4420638)包括3,781个人(来自Punjab的2,902和来自美国的879)。检查的六个SNP中有两个显示出令人信服的在这些亚洲印度裔人口中的复制。我们的研究证实了CETP rs3764261与高密度脂蛋白胆固醇(HDL-C)密切相关(p(= 2.03×10 −26 )。我们的研究结果还显示,在该亚洲印度裔队列中,APOA5-A4-C3-A1基因附近的BUD13-ZNF259的两个GWAS SNP(rs964184和rs12286037)与甘油三酸酯(TG)含量显着相关(rs964184:p = 1.74×10 −17 ; rs12286037:p = 1.58×10 -2 )。我们进一步研究了来自伦敦生命科学人群(LOLIPOP)的8,530名亚洲印第安人在染色体区域11q23.3(包含BUD13-ZNF259,APOA5-A4-C3-A1和SIK3基因)的195 kb区域中的45个SNP。 (英国)和SDS群组。在另外两个队列以及联合荟萃分析中,另外五个SNPs与TG显着相关。但是,TG的最强信号仍然是BUD13-ZNF259(rs964184:p = 1.06×10 -39 )。将来有针对性的深度测序和功能研究应增强我们对血脂异常和高甘油三酯血症(HTG)以及糖尿病和CAD中这些基因的临床相关性的了解。

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