医学
格尔德
孟德尔随机化
内科学
心力衰竭
疾病
观察研究
回流
心脏病学
肥胖
糖尿病
发病机制
临床试验
心脏病
逆概率加权
2型糖尿病
队列研究
仰卧位
共病
作者
Wansong Hu,YingXing Wu,Wanqian Yu,Ping Li
摘要
Abstract Aims While observational studies suggest an association between gastroesophageal reflux disease (GERD) and atrial fibrillation/flutter (AF/AFL), the causal relationship and mechanisms remain undefined. This study employed Mendelian randomization (MR) to assess bidirectional causal relationships and explore potential implications for heart failure (HF) risk. Methods and results A bidirectional two‐sample MR analysis was conducted using genome‐wide association study (GWAS) summary data from European populations (GERD: 129,080 cases and 473,524 controls; AF/AFL: 22,068 cases and 116,926 controls; Obesity: 4793 cases and 209,884 controls). Genetic instruments were selected for GERD and AF/AFL, with inverse variance weighting (IVW) as the primary analytical method to examine causality. Multivariable MR (MVMR) adjusted for obesity was performed to assess direct causal effects. Results IVW analysis demonstrated a significant causal effect of GERD on AF/AFL risk (OR = 1.373, 95% CI = 1.208–1.600, P = 0.017), which persisted after MVMR adjustment for obesity (OR = 1.303, 95% CI = 1.127–1.507, P < 0.001). Two‐way analysis indicated no reverse causality. Sensitivity analyses supported result robustness with minimal pleiotropy. Conclusions Genetic liability to GERD independently increases AF/AFL risk, unaffected by obesity pathways. Considering the well‐established role of AF/AFL in the pathogenesis and progression of HF, our findings position GERD as a potential modifiable target within the causal pathway. Identification and management of GERD may therefore contribute to reducing atrial arrhythmia burden and subsequent HF risk.
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