Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, 85 Park Road, Grafton, Auckland, 1023, New Zealand.
Department of Biochemistry, University of Otago, 710 Cumberland Street, Dunedin, 9012, New Zealand.
Arthritis Res Ther. 2019 Jan 9;21(1):13. doi: 10.1186/s13075-018-1787-5.
Sex-specific differences in the effect of genetic variants on serum urate levels have been described. The aim of this study was to systematically examine whether serum urate-associated genetic variants differ in their influence on gout risk in men and women.
This research was conducted using the UK Biobank Resource. Thirty single nucleotide polymorphisms (SNPs) associated with serum urate were tested for their association with gout in men and women of European ancestry, aged 40-69 years. Gene-sex interactions for gout risk were analysed using an interaction analysis in logistic regression models.
Gout was present in 6768 (4.1%) men and 574 (0.3%) women, with an odds ratio (95% confidence interval) for men 13.42 (12.32-14.62) compared with women. In men, experiment-wide association with gout was observed for 21 of the 30 serum urate-associated SNPs tested, and in women for three of the 30 SNPs. Evidence for gene-sex interaction was observed for ABCG2 (rs2231142) and PDZK1 (rs1471633), with the interaction in ABCG2 driven by an amplified effect in men and in PDZK1 by an absence of effect in women. Similar findings were observed in a sensitivity analysis which excluded pre-menopausal women. For the other SNPs tested, no significant gene-sex interactions were observed.
In a large population of European ancestry, ABCG2 and PDZK1 gene-sex interactions exist for gout risk, with the serum urate-raising alleles exerting a greater influence on gout risk in men than in women. In contrast, other serum urate-associated genetic variants do not demonstrate significant gene-sex interactions for gout risk.
已有研究描述了遗传变异对血清尿酸水平的影响在性别间存在差异。本研究旨在系统地检测血清尿酸相关遗传变异在男性和女性痛风风险中的影响是否存在差异。
本研究利用英国生物库资源进行。在年龄为 40-69 岁的欧洲裔男性和女性中,检测了 30 个与血清尿酸相关的单核苷酸多态性(SNP)与痛风的相关性。采用逻辑回归模型中的交互分析检验痛风风险的基因-性别相互作用。
男性中 6768 人(4.1%)和女性中 574 人(0.3%)患有痛风,男性的比值比(95%置信区间)为 13.42(12.32-14.62),与女性相比。在男性中,30 个血清尿酸相关 SNP 中有 21 个与痛风全基因组关联,而在女性中只有 3 个 SNP 与痛风全基因组关联。在 ABCG2(rs2231142)和 PDZK1(rs1471633)中观察到基因-性别相互作用的证据,ABCG2 中的相互作用是由于男性中效应放大,而 PDZK1 中则是由于女性中无效应。在排除了绝经前女性的敏感性分析中观察到了类似的发现。对于其他测试的 SNP,未观察到显著的基因-性别相互作用。
在一个欧洲裔的大型人群中,ABCG2 和 PDZK1 基因-性别相互作用与痛风风险有关,尿酸升高的等位基因对男性痛风风险的影响大于女性。相比之下,其他与血清尿酸相关的遗传变异在痛风风险中没有表现出显著的基因-性别相互作用。