Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study

被引:557
作者
Dehghan, Abbas [4 ]
Kottgen, Anna [6 ,7 ]
Yang, Qiong [8 ]
Hwang, Shih Jen [1 ,2 ,3 ]
Kao, W. H. Linda [6 ,7 ]
Rivadeneira, Fernando [5 ]
Boerwinkle, Eric [10 ,11 ]
Levy, Daniel [1 ,2 ,3 ]
Hofman, Albert [4 ]
Astor, Brad C. [6 ,7 ]
Benjamin, Emelia J. [9 ]
van Duijn, Cornelia M. [4 ]
Witteman, Jacqueline C. [4 ]
Coresh, Josef [6 ,7 ]
Fox, Caroline S. [1 ,2 ,3 ,12 ,13 ]
机构
[1] NHLBI, Framingham Heart Study, Framingham, MA 01702 USA
[2] Ctr Populat Studies, Framingham, MA 01702 USA
[3] NHLBI, Bethesda, MD 20892 USA
[4] Erasmus MC, Dept Epidemiol, Rotterdam, Netherlands
[5] Erasmus MC, Dept Internal Med, Rotterdam, Netherlands
[6] Johns Hopkins Univ, Dept Epidemiol, Baltimore, MD USA
[7] Johns Hopkins Univ, Welch Ctr Prevent Epidemiol & Clin Res, Baltimore, MD USA
[8] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02215 USA
[9] Boston Univ, Dept Cardiol, Sch Med, Boston, MA 02215 USA
[10] Univ Texas Houston, Hlth Sci Ctr, Ctr Human Genet, Houston, TX USA
[11] Univ Texas Houston, Hlth Sci Ctr, Inst Mol Med, Houston, TX USA
[12] Brigham & Womens Hosp, Div Endocrinol Hypertens & Diabet, Boston, MA 02115 USA
[13] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
D O I
10.1016/S0140-6736(08)61343-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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=11024) 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<5.0x10(-8)) or the Rotterdam cohort (p<1.0x10(-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=7.0x10(-168) and 2.9x10(-18) for white and black participants, respectively); missense rs2231142 in ABCG2 (p=2.5x10(-60) and 9.8x10(-4)), and rs17.65205 in SLC17A3 (p=3.3x10(-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=7.0x10(-14)), rs2231.142 (1.74, 1.51-1.99, p=3.3x10(-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 mu mol/L in the Framingham cohort, 269-386 mu mol/L in the Rotterdam cohort, and 303-426 mu mol/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. Funding Netherlands Organisation for Scientific Research (NWO); the National Heart, Lung, and Blood Institute.
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页码:1953 / 1961
页数:9
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