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原发性醛固酮增多症与心血管结局风险:全基因组关联和孟德尔随机化研究。

Primary Aldosteronism and Risk of Cardiovascular Outcomes: Genome-Wide Association and Mendelian Randomization Study.

机构信息

Department of Social Epidemiology, Graduate School of Medicine Kyoto University Kyoto Japan.

Hakubi Center for Advanced Research Kyoto University Kyoto Japan.

出版信息

J Am Heart Assoc. 2024 Aug 6;13(15):e034180. doi: 10.1161/JAHA.123.034180. Epub 2024 Aug 5.

DOI:10.1161/JAHA.123.034180
PMID:39101507
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11964008/
Abstract

BACKGROUND

Observational studies have reported associations between primary aldosteronism (PA) and cardiovascular outcomes, including coronary artery diseases (CAD), congestive heart failure (CHF), and stroke. However, establishing causality remains a challenge due to the lack of randomized controlled trial data on this topic. We thus aimed to investigate the causal relationship between PA and the risk of developing CAD, CHF, and stroke.

METHODS AND RESULTS

Cross-ancestry meta-analysis of genome-wide association studies combining East Asian and European ancestry (1560 PA cases and 742 139 controls) was conducted to identify single-nucleotide variants that are associated with PA. Then, using the identified genetic variants as instrumental variables, we conducted the 2-sample Mendelian randomization analysis to investigate the causal relationship between PA and incident CAD, CHF, and stroke among both East Asian and European ancestry. Summary association results were extracted from large genome-wide association studies consortia. Our cross-ancestry meta-analysis of East Asian and European populations identified 7 genetic loci significantly associated with the risk of PA, for which the genes nearest to the lead variants were , , , , , , and . Among the East Asian population, the pooled odds ratio estimates using these 7 genetic instruments of PA were 1.07 (95% CI, 1.03-1.11) for CAD, 1.10 (95% CI, 1.01-1.20) for CHF, and 1.13 (95% CI, 1.09-1.18) for stroke. The results were consistent among the European population.

CONCLUSIONS

Our 2-sample Mendelian randomization study revealed that PA had increased risks of CAD, CHF, and stroke. These findings highlight that early and active screening of PA is critical to prevent future cardiovascular events.

摘要

背景

观察性研究报告称原发性醛固酮增多症(PA)与心血管结局之间存在关联,包括冠状动脉疾病(CAD)、充血性心力衰竭(CHF)和中风。然而,由于缺乏关于该主题的随机对照试验数据,确定因果关系仍然具有挑战性。因此,我们旨在研究 PA 与 CAD、CHF 和中风风险之间的因果关系。

方法和结果

对东亚和欧洲血统的全基因组关联研究进行跨血统荟萃分析(PA 病例 1560 例,对照组 742139 例),以确定与 PA 相关的单核苷酸变异。然后,使用鉴定出的遗传变异作为工具变量,我们进行了两样本孟德尔随机化分析,以调查东亚和欧洲血统人群中 PA 与 CAD、CHF 和中风事件之间的因果关系。汇总关联结果从大型全基因组关联研究联盟中提取。我们对东亚和欧洲人群的跨血统荟萃分析确定了 7 个与 PA 风险显著相关的遗传位点,其中最接近先导变异的基因是 、 、 、 、 、 和 。在东亚人群中,使用这 7 个 PA 遗传工具的汇总优势比估计值为 CAD 为 1.07(95%CI,1.03-1.11),CHF 为 1.10(95%CI,1.01-1.20),中风为 1.13(95%CI,1.09-1.18)。在欧洲人群中,结果一致。

结论

我们的两样本孟德尔随机化研究表明,PA 增加了 CAD、CHF 和中风的风险。这些发现强调,早期和积极筛查 PA 对于预防未来的心血管事件至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8168/11964008/00fe61ba9ec1/JAH3-13-e034180-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8168/11964008/52baf14460b3/JAH3-13-e034180-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8168/11964008/00fe61ba9ec1/JAH3-13-e034180-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8168/11964008/52baf14460b3/JAH3-13-e034180-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8168/11964008/00fe61ba9ec1/JAH3-13-e034180-g002.jpg

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