Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Hum Genet. 2010 Feb;127(2):223-9. doi: 10.1007/s00439-009-0765-z. Epub 2009 Nov 14.
Taiwanese aborigines have a high prevalence of hyperuricemia and gout. Uric acid levels and urate excretion have correlated with dopamine-induced glomerular filtration response. MAOs represent one of the major renal dopamine metabolic pathways. We aimed to identify the monoamine oxidase A (MAOA, Xp11.3) gene variants and MAO-A enzyme activity associated with gout risk. This study was to investigate the association between gout and the MAOA single-nucleotide polymorphisms (SNPs) rs5953210, rs2283725, and rs1137070 as well as between gout and the COMT SNPs rs4680 Val158Met for 374 gout cases and 604 controls. MAO-A activity was also measured. All three MAOA SNPs were significantly associated with gout. A synonymous MAOA SNP, rs1137070 Asp470Asp, located in exon 14, was associated with the risk of having gout (P = 4.0 x 10(-5), adjusted odds ratio 1.46, 95% confidence intervals [CI]: 1.11-1.91). We also showed that, when compared to individuals with the MAOA GAT haplotype, carriers of the AGC haplotype had a 1.67-fold (95% CI: 1.28-2.17) higher risk of gout. Moreover, we found that MAOA enzyme activity correlated positively with hyperuricemia and gout (P for trend = 2.00 x 10(-3) vs. normal control). We also found that MAOA enzyme activity by rs1137070 allele was associated with hyperuricemia and gout (P for trend = 1.53 x 10(-6) vs. wild-type allele). Thus, our results show that some MAOA alleles, which have a higher enzyme activity, predispose to the development of gout.
台湾原住民高尿酸血症和痛风的患病率很高。尿酸水平和尿酸排泄与多巴胺诱导的肾小球滤过反应相关。MAOs 代表肾脏多巴胺代谢的主要途径之一。我们旨在确定与痛风风险相关的单胺氧化酶 A (MAOA, Xp11.3) 基因变异和 MAO-A 酶活性。本研究旨在调查痛风与 MAOA 单核苷酸多态性 (SNP) rs5953210、rs2283725 和 rs1137070 以及与 COMT SNP rs4680 Val158Met 之间的关联,共纳入 374 例痛风病例和 604 例对照。还测量了 MAO-A 活性。所有三个 MAOA SNP 均与痛风显著相关。位于外显子 14 中的同义 MAOA SNP rs1137070 Asp470Asp 与痛风风险相关(P=4.0×10(-5),调整后的比值比 1.46,95%置信区间 [CI]:1.11-1.91)。我们还表明,与 MAOA GAT 单倍型个体相比,AGC 单倍型携带者痛风的风险增加了 1.67 倍(95%CI:1.28-2.17)。此外,我们发现 MAOA 酶活性与高尿酸血症和痛风呈正相关(趋势 P=2.00×10(-3) vs. 正常对照)。我们还发现 MAOA 酶活性与 rs1137070 等位基因与高尿酸血症和痛风相关(趋势 P=1.53×10(-6) vs. 野生型等位基因)。因此,我们的研究结果表明,一些 MAOA 等位基因,其具有更高的酶活性,容易发展为痛风。