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Updated: Jan 8, 2026

Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice
Published on: May 2, 2025
Investigating the Causal Association Between Helicobacter pylori Infection and Diabetic Nephropathy: A Two-Sample
1Department of Endocrinology, Changzhou Hospital Affiliated to Nanjing University of Chinese Medicine, Changzhou 213003, China.
Objective:
Diabetic nephropathy (DN) is a leading cause of end-stage renal disease. This study investigated the potential causal association between Helicobacter pylori infection and DN.
Methods:
The two-sample Mendelian randomization (MR) methodology and public data on DN and H. pylori infection from genome-wide association studies (GWASs) were used. The primary MR analytical method was the inverse variance weighted (IVW), complemented by additional methods such as MR-Egger, weighted median, and weighted mode. Results were validated through extensive sensitivity analyses, including tests for pleiotropy (PhenoScanner), directionality (bidirectional MR and Steiger test), and heterogeneity. A false discovery rate (FDR) was applied to correct for multiple testing.
Results:
Among 7 H. pylori antibody markers, only genetically predicted catalase antibody levels showed a suggestive protective association with DN (odds ratio [OR] = 0.90, 95% confidence interval [CI]: 0.82-0.99, p = 0.03). However, this association did not withstand correction for multiple testing (P-FDR = 0.21). No significant causal effects were observed for other antibody markers. Sensitivity analyses found no evidence of horizontal pleiotropy and consistently supported a causal direction from H. pylori exposure to DN.
Conclusion:
Our findings provide suggestive evidence for a potential causal link between the host immune response to H. pylori catalase and a lower risk of DN. This specific, biologically plausible pathway warrants further investigation in larger, more diverse populations to confirm its potential role in the pathogenesis of DN.
