AI Article Synopsis

  • - The study explored the causal relationship between primary aldosteronism (PA) and cardiovascular diseases such as coronary artery disease (CAD), congestive heart failure (CHF), and stroke, using a cross-ancestry meta-analysis of genetic data.
  • - The researchers identified 7 genetic loci linked to PA risk through an extensive analysis of East Asian and European ancestry samples, finding increased risk estimates for CAD, CHF, and stroke among individuals with PA.
  • - The findings suggest that PA significantly raises the risk of various cardiovascular issues, underlining the importance of early screening and intervention for individuals at risk.

Article 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.

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Source
http://dx.doi.org/10.1161/JAHA.123.034180DOI Listing

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