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首页> 外文期刊>The Lancet >Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study.
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Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study.

机译:三种基因座与尿酸浓度和痛风风险的关联:全基因组关联研究。

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BACKGROUND: Hyperuricaemia, a highly heritable trait, is a key risk factor for gout. We aimed to identify novel genes associated with serum uric acid concentration and gout. METHODS: Genome-wide association studies were done for serum uric acid in 7699 participants in the Framingham cohort and in 4148 participants in the Rotterdam cohort. Genome-wide significant single nucleotide polymorphisms (SNPs) were replicated in white (n=11 024) and black (n=3843) individuals who took part in the study of Atherosclerosis Risk in Communities (ARIC). The SNPs that reached genome-wide significant association with uric acid in either the Framingham cohort (p<5.0 x 10(-8)) or the Rotterdam cohort (p<1.0 x 10(-7)) were evaluated with gout. The results obtained in white participants were combined using meta-analysis. FINDINGS: Three loci in the Framingham cohort and two in the Rotterdam cohort showed genome-wide association with uric acid. Top SNPs in each locus were: missense rs16890979 in SLC2A9 (p=7.0 x 10(-168) and 2.9 x 10(-18) for white and black participants, respectively); missense rs2231142 in ABCG2 (p=2.5 x 10(-60) and 9.8 x 10(-4)), and rs1165205 in SLC17A3 (p=3.3 x 10(-26) and 0.33). All SNPs were direction-consistent with gout in white participants: rs16890979 (OR 0.59 per T allele, 95% CI 0.52-0.68, p=7.0 x 10(-14)), rs2231142 (1.74, 1.51-1.99, p=3.3 x 10(-15)), and rs1165205 (0.85, 0.77-0.94, p=0.002). In black participants of the ARIC study, rs2231142 was direction-consistent with gout (1.71, 1.06-2.77, p=0.028). An additive genetic risk score of high-risk alleles at the three loci showed graded associations with uric acid (272-351 mumol/L in the Framingham cohort, 269-386 mumol/L in the Rotterdam cohort, and 303-426 mumol/L in white participants of the ARIC study) and gout (frequency 2-13% in the Framingham cohort, 2-8% in the Rotterdam cohort, and 1-18% in white participants in the ARIC study). INTERPRETATION: We identified three genetic loci associated with uric acid concentration and gout. A score based on genes with a putative role in renal urate handling showed a substantial risk for gout.
机译:背景:高尿酸血症是一种高度可遗传的性状,是痛风的关键危险因素。我们旨在鉴定与血清尿酸浓度和痛风有关的新基因。方法:在Framingham队列的7699名参与者和鹿特丹队列的4148名参与者中进行了全基因组关联的血清尿酸研究。全基因组范围内的显着单核苷酸多态性(SNP)在参与社区动脉粥样硬化风险研究(ARIC)的白人(n = 11 024)和黑人(n = 3843)个体中复制。用痛风评估在Framingham队列(p <5.0 x 10(-8))或Rotterdam队列(p <1.0 x 10(-7))中与尿酸达到全基因组显着关联的SNP。白人参与者获得的结果通过荟萃分析进行合并。结果:Framingham队列中的三个基因座和Rotterdam队列中的两个基因座显示了全基因组与尿酸的关联。每个基因座中的最高SNP为:SLC2A9中的错义rs16890979(白人和黑人参与者分别为p = 7.0 x 10(-168)和2.9 x 10(-18)); ABCG2中的错义rs2231142(p = 2.5 x 10(-60)和9.8 x 10(-4)),以及SLC17A3中的rs1165205(p = 3.3 x 10(-26)和0.33)。白人参与者的所有SNPs与痛风的方向一致:rs16890979(每个T等位基因OR 0.59,95%CI 0.52-0.68,p = 7.0 x 10(-14)),rs2231142(1.74,1.51-1.99,p = 3.3 x 10(-15))和rs1165205(0.85,0.77-0.94,p = 0.002)。在ARIC研究的黑人参与者中,rs2231142与痛风的方向一致(1.71、1.06-2.77,p = 0.028)。在三个基因座处的高风险等位基因的加性遗传风险评分显示与尿酸有分级关联(在弗雷明汉队列中为272-351 mumol / L,在鹿特丹队列中为269-386 mumol / L,和303-426 mumol / L ARIC研究的白人参与者)和痛风(Framingham队列的频率为2-13%,鹿特丹队列的频率为2-8%,ARIC研究的白人参与者为1-18%)。解释:我们确定了三个与尿酸浓度和痛风有关的遗传基因座。基于在肾尿酸盐处理中具有推定作用的基因的评分显示出痛风的严重风险。

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