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Association of Angina, Myocardial Infarction and Atrial Fibrillation-A Bidirectional Mendelian Randomization Study
Lu Chen1,2, Yan He2, Ying Wang2
1Department of Cardiology, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Insights
Coronary atherosclerosis and heart attacks may increase atrial fibrillation risk. Atrial fibrillation may also raise coronary atherosclerosis risk, suggesting a bidirectional causal link.
Area of Science:
- Cardiovascular Medicine
- Genetics
- Epidemiology
Background:
- Coronary heart disease (CHD) and atrial fibrillation (AF) are closely linked.
- Observational studies limit establishing causal relationships between CHD and AF.
- Causal links between coronary atherosclerosis (CAAs), angina pectoris, myocardial infarction (MI), and AF require investigation.
Purpose of the Study:
- To investigate the causal relationships between CAAs, angina, MI, and AF.
- To utilize Mendelian randomization to assess causality between cardiovascular conditions and AF.
Main Methods:
- Two-sample Mendelian randomization (TSMR) methodology.
- Leveraging genetic variation to infer causal relationships.
- Adherence to Mendelian randomization assumptions for validity.
Main Results:
- Genetic predisposition suggests CAAs, angina, and MI increase susceptibility to AF.
- Evidence indicates AF may reciprocally elevate the risk of CAAs.
- Findings suggest a potential bidirectional causal relationship.
Conclusions:
- Patients with CHD should have regular cardiac rhythm monitoring.
- Patients with AF should receive feasible anticoagulant and antiplatelet therapy.
- The study offers practical implications for clinical management of cardiovascular diseases.
Abstract:
Aims/Background Coronary heart disease (CHD) and atrial fibrillation (AF) exhibit a close relationship, yet the existing body of research predominantly relies on observational study methodologies, posing challenges in establishing causal relationships. The objective of our study is to investigate the causal linkages between coronary atherosclerosis (CAAs), angina pectoris, myocardial infarction (MI), and AF. Methods This study utilizes a two-sample Mendelian randomization (TSMR) methodology, leveraging genetic variation as a means of evaluating causality. Mendelian randomization is grounded in three primary assumptions: (1) the genetic variant is linked to the exposure, (2) the genetic variant is independent of confounding factors, and (3) the genetic variant influences the outcome solely through the exposure. Results The results of our study suggest a genetic predisposition in which CAAs, angina, and MI may enhance susceptibility to AF, while AF may reciprocally elevate the risk of CAAs. Conclusion In light of these findings, it is recommended that patients with CHD undergo regular cardiac rhythm monitoring, and that patients with AF receive anticoagulant and antiplatelet therapy whenever feasible. This study posits a practical implication for clinical practice.
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