Mendelian Randomization Analysis of Genetic Proxies of Thiazide Diuretics and the Reduction of Kidney Stone Risk

孟德尔随机化 噻嗪 医学 氢氯噻嗪 优势比 血压 内科学 全基因组关联研究 肾结石 内分泌学 单核苷酸多态性 遗传学 生物 遗传变异 基因型 基因
作者
Jefferson L. Triozzi,Ryan S. Hsi,Guanchao Wang,Elvis A. Akwo,Lee Wheless,Hua‐Chang Chen,Ran Tao,Talat Alp Ikizler,Cassianne Robinson‐Cohen,Adriana M. Hung,VA Million Veteran Program,Sumitra Muralidhar,Jennifer Moser,Jennifer E. Deen,Philip S. Tsao,J. Michael Gaziano,Elizabeth R. Hauser,Amy M. Kilbourne,Shiuh‐Wen Luoh,Michael Edwin Matheny
出处
期刊:JAMA network open [American Medical Association]
卷期号:6 (11): e2343290-e2343290 被引量:39
标识
DOI:10.1001/jamanetworkopen.2023.43290
摘要

Importance: Clinical trial data have called into question the efficacy of thiazide diuretics for the prevention of kidney stones. Objective: To identify whether there is an association between genetic proxies of thiazide diuretics and the risk of kidney stones. Design, Setting, and Participants: This genetic association study undertook a mendelian randomization analysis of derived exposures and outcomes from genome-wide association study summary statistics. Genetic proxies of thiazide diuretics were derived from the International Consortium for Blood Pressure. Kidney stone cases and controls were derived from the Million Veteran Program, UK Biobank, and the FinnGen study. These cross-sectional designs do not report a duration of follow-up. Data analysis was performed in May 2023. Exposure: Genetic proxies of thiazide diuretics were genetic variants in the thiazide-sensitive sodium chloride cotransporter gene associated with systolic blood pressure. Genetic proxies of β-blockers and systolic blood pressure served as negative controls. Main Outcomes and Measures: The main outcome was the odds of kidney stones. The secondary outcomes were serum laboratory values relevant to the treatment of kidney stones. Results: The main analysis included up to 1 079 657 individuals, including 50 832 kidney stone cases and 1 028 825 controls. In a meta-analysis of all cohorts, genetic proxies of thiazide diuretics were associated with a lower odds of kidney stones (OR, 0.85; 95% CI, 0.81-0.89; P < .001). Genetic proxies of β-blockers (OR, 1.02; 95% CI, 0.96-1.07; P = .52) and systolic blood pressure (OR, 1.00; 95% CI, 1.00-1.01; P = .49) were not associated with kidney stones. Genetic proxies of thiazide diuretics were associated with higher serum calcium (β [SE], 0.051 [0.0092]; P < .001) and total cholesterol (β [SE], 0.065 [0.015]; P < .001), but lower serum potassium (β [SE], -0.073 [0.022]; P < .001). Conclusions and Relevance: In this genetic association study, genetic proxies of thiazide diuretics were associated with reduced kidney stone risk. This finding reflects a drug effect over the course of a lifetime, unconstrained by the limited follow-up period of clinical trials.
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