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血清尿酸相关遗传变异是否影响服用利尿剂人群的痛风风险?英国生物库分析。

Do Serum Urate-associated Genetic Variants Influence Gout Risk in People Taking Diuretics? Analysis of the UK Biobank.

机构信息

R.K. Narang, MBChB, G. Gamble, MSc, N. Dalbeth, FRACP, Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland.

A.J. Phipps-Green, MSc, R. Topless, BSc, M. Cadzow, PhD, T.R. Merriman, PhD, Department of Biochemistry, University of Otago, Dunedin.

出版信息

J Rheumatol. 2020 Nov 1;47(11):1704-1711. doi: 10.3899/jrheum.191005. Epub 2020 Feb 1.

Abstract

OBJECTIVE

The aim of this study was to determine whether serum urate (SU)-associated genetic variants differ in their influence on gout risk in people taking a diuretic compared to those not taking a diuretic.

METHODS

This research was conducted using the UK Biobank Resource (n = 359,876). Ten SU-associated single-nucleotide polymorphisms (SNP) were tested for their association with gout according to diuretic use. Gene-diuretic interactions for gout association were tested using a genetic risk score (GRS) and individual SNP by logistic regression adjusting for relevant confounders.

RESULTS

After adjustment, use of a loop diuretic was positively associated with prevalent gout (OR 2.34, 95% CI 2.08-2.63), but thiazide diuretics were inversely associated with prevalent gout (OR 0.60, 95% CI 0.55-0.66). Compared with a lower GRS (< mean), a higher GRS (≥ mean) was positively associated with gout in those not taking diuretics (OR 2.63, 2.49-2.79), in those taking loop diuretics (OR 2.04, 95% CI 1.65-2.53), in those taking thiazide diuretics (OR 2.70, 2.26-3.23), and in those taking thiazide-like diuretics (OR 2.11, 95% CI 1.37-3.25). No nonadditive gene-diuretic interactions were observed.

CONCLUSION

In people taking diuretics, SU-associated genetic variants contribute strongly to gout risk, with a similar effect to that observed in those not taking a diuretic. These findings suggest that the contribution of genetic variants is not restricted to people with "primary" gout, and that genetic variants can play an important role in gout susceptibility in the presence of other risk factors.

摘要

目的

本研究旨在确定血清尿酸(SU)相关遗传变异在利尿剂使用者和非利尿剂使用者中的痛风风险影响方面是否存在差异。

方法

本研究使用英国生物库资源(n=359876)进行。根据利尿剂的使用情况,对 10 个 SU 相关的单核苷酸多态性(SNP)与痛风的相关性进行了检测。通过调整相关混杂因素的逻辑回归,使用遗传风险评分(GRS)和个体 SNP 对痛风关联的基因-利尿剂相互作用进行了测试。

结果

调整后,使用袢利尿剂与现患痛风呈正相关(OR 2.34,95%CI 2.08-2.63),而噻嗪类利尿剂与现患痛风呈负相关(OR 0.60,95%CI 0.55-0.66)。与较低的 GRS(<平均值)相比,在不使用利尿剂的人群中,较高的 GRS(≥平均值)与痛风呈正相关(OR 2.63,95%CI 2.49-2.79),在使用袢利尿剂的人群中(OR 2.04,95%CI 1.65-2.53),在使用噻嗪类利尿剂的人群中(OR 2.70,95%CI 2.26-3.23),以及在使用噻嗪类样利尿剂的人群中(OR 2.11,95%CI 1.37-3.25)。未观察到非加性基因-利尿剂相互作用。

结论

在使用利尿剂的人群中,SU 相关的遗传变异对痛风风险的贡献很大,与未使用利尿剂的人群观察到的效果相似。这些发现表明,遗传变异的贡献不仅限于“原发性”痛风患者,而且在存在其他危险因素的情况下,遗传变异可能在痛风易感性中发挥重要作用。

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