Renal Division, Freiburg University Hospital, Freiburg, Germany.
Nat Genet. 2013 Feb;45(2):145-54. doi: 10.1038/ng.2500. Epub 2012 Dec 23.
Elevated serum urate concentrations can cause gout, a prevalent and painful inflammatory arthritis. By combining data from >140,000 individuals of European ancestry within the Global Urate Genetics Consortium (GUGC), we identified and replicated 28 genome-wide significant loci in association with serum urate concentrations (18 new regions in or near TRIM46, INHBB, SFMBT1, TMEM171, VEGFA, BAZ1B, PRKAG2, STC1, HNF4G, A1CF, ATXN2, UBE2Q2, IGF1R, NFAT5, MAF, HLF, ACVR1B-ACVRL1 and B3GNT4). Associations for many of the loci were of similar magnitude in individuals of non-European ancestry. We further characterized these loci for associations with gout, transcript expression and the fractional excretion of urate. Network analyses implicate the inhibins-activins signaling pathways and glucose metabolism in systemic urate control. New candidate genes for serum urate concentration highlight the importance of metabolic control of urate production and excretion, which may have implications for the treatment and prevention of gout.
血清尿酸浓度升高可导致痛风,这是一种常见且疼痛的炎症性关节炎。通过对全球尿酸遗传学联合会(GUGC)中超过 14 万名欧洲血统个体的数据进行联合分析,我们在与血清尿酸浓度相关的研究中发现并复制了 28 个全基因组显著相关位点(18 个新区域位于 TRIM46、INHBB、SFMBT1、TMEM171、VEGFA、BAZ1B、PRKAG2、STC1、HNF4G、A1CF、ATXN2、UBE2Q2、IGF1R、NFAT5、MAF、HLF、ACVR1B-ACVRL1 和 B3GNT4 内或附近)。在非欧洲血统个体中,许多这些位点的关联程度相似。我们进一步对这些位点与痛风、转录表达和尿酸排泄分数的关联进行了特征描述。网络分析提示抑制素-激活素信号通路和葡萄糖代谢与全身尿酸控制有关。血清尿酸浓度的新候选基因突出了尿酸生成和排泄的代谢控制的重要性,这可能对痛风的治疗和预防具有重要意义。