Gastroesophageal reflux disease increases the risk of rheumatoid arthritis: a bidirectional two-sample Mendelian randomization study

• Published in: Scientific reports 2024-08, Vol.14 (1), p.17796-11, Article 17796
• Main Authors: Yuan, Quan, Shen, Zixiong, Zhang, Jiujiang, Liu, Qing, Whang, Huimin, Li, Yang
• Format: Article
• Language: English
• Subjects: 692/308; 692/4020; 692/4023; 692/499; Arthritis, Rheumatoid - genetics; Autoimmune diseases; Bidirectional; Causal effect; Gastroesophageal reflux; Gastroesophageal Reflux - genetics; Gastroesophageal reflux disease; Genetic Predisposition to Disease; Genome-wide association studies; Genome-Wide Association Study; Genomic analysis; Humanities and Social Sciences; Humans; Mendelian randomization; Mendelian Randomization Analysis; multidisciplinary; Observational studies; Odds Ratio; Polymorphism, Single Nucleotide; Rheumatoid arthritis; Risk Factors; Science; Science (multidisciplinary)
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-64966-w

Rheumatoid arthritis (RA) is a common autoimmune disease, and some observational studies have indicated an association between Gastroesophageal Reflux Disease (GERD) and RA. However, the causal relationship between the two remains uncertain. We used Mendelian randomization (MR) to assess the causal relationship between GERD and RA. Two-sample Mendelian randomization analysis was performed using pooled data from large-scale genome-wide association studies. In addition, we performed multivariate MR analyses to exclude confounding factors between GERD and RA, including smoking quantity, drinking frequency, BMI, depression, and education attainment. The MR results for GERD on RA suggested a causal effect of the genetic susceptibility of GERD on RA (discovery dataset, IVW, odds ratio [OR] = 1.41, 95% confidence interval [CI] 1.22–1.63, p  = 2.81 × 10 −6 ; validation dataset, IVW, OR = 1.38, 95% CI 1.23–1.55, P  = 1.76 × 10 −8 ). Multivariate MR analysis also supports this result. But the results of the reverse MR analysis did not reveal compelling evidence that RA can increase the risk of developing GERD. Our bidirectional Two-Sample Mendelian randomization analysis and multivariate MR analysis provide support for the causal effect of GERD on RA. This discovery could offer new insights for the prevention and treatment of RA.