Mendelian randomization reveals a 5% increased urolithiasis incidence linked to Rabeprazole and sensitivity analyses support findings.
Observational studies suggest that proton pump inhibitors (PPIs) increase the risk of urolithiasis (UL). However, the causal correlation between the 2 is still unclear. To examine the causal relationship between PPIs and UL, this study used 2-sample Mendelian randomization. The genome-wide association studies (GWAS) of Omeprazole, Esomeprazole, Lansoprazole, and Rabeprazole medication can be obtained from GWAS catalog. Furthermore, we acquired UL-related single nucleotide polymorphisms from the integrative epidemiology unit OpenGWAS. To access the causality of PPIs and UL, we performed a 2-sample Mendelian randomization. The primary approach to analysis was random-effects inverse variance weighting. In addition, we also used another dataset of UL to further verify the causal role. We discovered that there was a 5% increase in the incidence of UL in the use of Rabeprazole medication (test group: odd ratio [OR] = 1.053, 95% confidence interval [CI]: 1.005–1.103; validation group: OR = 1.051, 95% CI: 1.003–1.101). Furthermore, we found that Esomeprazole was negatively correlated with UL in the inverse variance weighting method (test group: OR = 0.914, 95% CI: 0.841–0.993; validation group: OR = 0.943, 95% CI: 0.890–0.999). The results of sensitivity analyses supported our conclusion. In conclusion, our results suggest a causal relationship of PPIs to UL. For patients requiring antiacid therapy, esomeprazole may be a better option than Rabeprazole, especially in patients with high-risk factors for urolithiasis.
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Guo et al. (2025) studied this question.
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