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Updated: Jun 25, 2025

Estimating Bilateral Atrial Function by Cardiovascular Magnetic Resonance Feature Tracking in Patients with Paroxysmal Atrial Fibrillation
Published on: July 20, 2022
Gastroesophageal reflux disease and atrial fibrillation: a bidirectional Mendelian randomization study
Xiaoli Chen1,2, Aihua Li1,2, Yuanyuan Kuang1,2
1Department of Cardiovascular Medicine, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Insights
Gastroesophageal reflux disease (GERD) causally increases the risk of atrial fibrillation (AF). However, this study found no evidence that atrial fibrillation causes GERD, clarifying the directional relationship between these conditions.
Area of Science:
- Cardiology
- Gastroenterology
- Genetic Epidemiology
Background:
- Observational studies suggest a link between gastroesophageal reflux disease (GERD) and atrial fibrillation (AF).
- The causal direction and potential confounding factors (obesity, sleep-disordered breathing) remain unclear.
- Bidirectional Mendelian randomization (MR) is employed to investigate causality, mitigating confounding and reverse causation.
Purpose of the Study:
- To determine the causal effect of GERD on AF risk.
- To investigate the causal effect of AF on GERD risk.
Main Methods:
- Utilized summary data from genome-wide association studies (GWAS) for GERD and AF.
- Performed bidirectional Mendelian randomization (MR) using genetic variations as instrumental variables.
- Employed inverse variance weighted (IVW), MR-PRESSO, weighted median, and MR-Egger regression for robust analysis.
Main Results:
- Genetic liability to GERD was associated with an increased risk of AF (OR = 1.339, p < 0.001).
- After outlier removal, genetically predicted AF did not show a significant association with an elevated risk of GERD (p = 0.351).
Conclusions:
- GERD exerts a causal effect on the risk of developing AF.
- No evidence supports a causal effect of AF on the risk of GERD.
Abstract:
Background: In observational studies, gastroesophageal reflux disease (GERD) is linked to atrial fibrillation (AF). It is uncertain whether the relationship is due to GERD-induced AF or GERD caused by AF, or confusion with factors related to GERD and AF such as obesity and sleep-disordered breathing. We applied bidirectional Mendelian randomization (MR), in which genetic variations are used as instrumental variables to resolve confounding and reverse causation issues, to determine the causal effect between GERD and AF. Methods: Using summary data from the GERD and AF genome-wide association study (GWAS), a bidirectional MR was performed to estimate the causative impact of GERD on AF risk and AF on GERD risk. The GWAS of GERD meta-analysis comprised 78707 cases and 288734 controls. GWAS summary data for AF, including 45766 AF patients and 191924 controls, were used to genetically predicted AF. The inverse variance weighted (IVW) method was the major MR approach used. MR-PRESSO was implemented to detect heterogeneity and correct the effect of outliers. Weighted median and MR-Egger regression were applied to test heterogeneity and pleiotropy. Results: The genetic instruments of GERD related to increasing the risk of AF, with an OR of 1.339 (95% CI: 1.242-1.444, p < 0.001). However, after removing the outlier 8 SNPs, genetically predicted AF was not associated with an elevated risk of GERD (p = 0.351). Conclusions: Our result suggested that GERD had a causal effect on AF. However, no evidence was identified that AF elevated the risk of GERD.
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