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Author Spotlight: A Pharmacodissection Approach to Uncover Mechanisms in Cardiovascular Disease Risk Populations
Published on: July 21, 2023
Associations between high-altitude adaptation and risk of cardiovascular diseases: a bidirectional Mendelian
Yuqing Jiang1, Jie Ping2, Hao Lu2
1Collaborative Innovation Center for Personalized Cancer Medicine, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing City, Jiangsu Province, 211166, People's Republic of China.
Insights
High-altitude adaptation (HAA) causally reduces coronary artery disease (CAD) risk. This study found no evidence that cardiovascular diseases (CVDs) affect HAA, offering insights for CAD prevention strategies.
Area of Science:
- Genetics
- Cardiovascular Medicine
- Human Adaptation
Background:
- High-altitude adaptation (HAA) is linked to lower cardiovascular disease (CVD) risks.
- The causal relationship and directionality between HAA and CVDs remain unclear.
Purpose of the Study:
- To investigate the potential causal links between HAA and six major CVDs using Mendelian randomization.
- To determine if HAA influences the risk of coronary artery disease (CAD), cerebral aneurysm, ischemic stroke, peripheral artery disease, arrhythmia, and atrial fibrillation.
Main Methods:
- Utilized two-sample bidirectional Mendelian randomization (MR) with genome-wide association study summary data.
- Performed sensitivity analyses including MR-Egger regression, MR-PRESSO, Cochran's Q tests, and leave-one-out analyses to ensure robustness and assess pleiotropy.
Main Results:
- Genetically predicted HAA showed a significant causal association with reduced risk of CAD (OR=0.029).
- No statistically significant causal relationships were found between CVDs and HAA in the reverse direction.
Conclusions:
- HAA has a causal protective effect on the risk of developing CAD.
- Evidence suggests CVDs do not causally influence HAA, supporting HAA as a factor in CAD prevention.
Abstract:
High-altitude adaptation (HAA) was reported to be significantly associated with reduced risks for multiple cardiovascular diseases (CVDs). However, the causality and direction of the associations are largely uncharacterized. We aimed to examine the potential causal relationships between HAA and six types of CVD, including coronary artery disease (CAD), cerebral aneurysm, ischemic stroke, peripheral artery disease, arrhythmia and atrial fibrillation. We obtained the summary data from largest available genome-wide association study of HAA and six types of CVD. Two-sample bidirectional Mendelian randomization (MR) analyses were performed to infer the causality between them. In the sensitivity analyses, MR-Egger regression analyses and MR-Pleiotropy RESidual Sum and Outlier (MR-PRESSO) global analyses were used to assess the pleiotropic effects; Cochran's Q tests were used to test the heterogeneity by inverse variance-weighted (IVW) and MR-Egger methods; and the leave-one-out analyses were used to examine whether some single nucleotide polymorphisms (SNPs) could influence the results independently. The MR main analyses showed that the genetically instrumented HAA was significantly causally associated with the reduced risks of CAD (odds ratio [OR] = 0.029; 95% confidence interval [CI] = 0.004-0.234; P = 8.64 × 10-4). In contrast, there was no statistically significant relationship between CVDs and HAA. Our findings provide evidence for the causal effects of HAA on the reduced risks of CAD. However, there is no causality of CVDs on HAA. These findings might be helpful in developing the prevention and intervention strategies for CAD.
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