已发表论文

口腔微生物群与妊娠期糖尿病之间的因果关联:一项两样本孟德尔随机化研究

 

Authors Jin H, Wang Y, Li H, Cheng Y, Ma Y

Received 28 March 2025

Accepted for publication 1 August 2025

Published 30 August 2025 Volume 2025:17 Pages 2777—2791

DOI https://doi.org/10.2147/IJWH.S531088

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Everett Magann

Hui Jin,* Yapei Wang,* Hongbin Li, Yinqin Cheng, Yumin Ma

Department of Internal Medicine, The Second People’s Hospital of Nantong, Nantong, 226000, People’s Republic of China

*These authors contributed equally to this work

Correspondence: Yumin Ma, Department of Internal Medicine, The Second People’s Hospital of Nantong, Nantong, 226000, People’s Republic of China, Tel +86-13861995848, Email 397318346@qq.com

Background: Gestational diabetes mellitus (GDM) is associated with adverse pregnancy outcomes. The oral microbiota, influenced by genetic factors, may play a role in GDM development, but the causal association remains unclear.
Methods: We employed a two-sample Mendelian randomization (MR) approach using Genome-Wide Association Study (GWAS) data on GDM from FINN cohort data (ID: finngen_R10_GEST_DIABETES) and GWAS data on the Oral microbiota from the Danish ADDITION-PRO cohort. We screened SNPs significantly associated with Oral microbiota abundance as instrumental variables (IVs) and assessed their association with GDM risk. The study primarily used an inverse variance weighting (IVW) approach and further applied MR-Egger regression, weighted median, and weighted mode methods for robustness testing. Sensitivity analyses were conducted to evaluate the impact of heterogeneity and pleiotropy, including MR-Egger, MR-PRESSO, Cochran’s Q, and leave-one-out methods.
Results: We identified 267 IVs associated with Oral microbiota abundance. IVW analysis revealed a positive causal association between Genus Schaalia and GDM risk (OR = 1.03, 95% CI: 1.01– 1.06, P = 0.02) and a negative association between Genus Haemophilus and GDM risk (OR = 0.96, 95% CI: 0.93– 1.00, P = 0.034). Sensitivity analyses confirmed the robustness of these two results, showing no evidence of heterogeneity or pleiotropy.
Conclusion: Our study provides evidence for a causal association between Genus Schaalia and Haemophilus and GDM risk. This highlights the potential role of the Oral microbiota in GDM pathogenesis and suggests potential targets for GDM prevention and treatment.

Keywords: oral microbiota, gestational diabetes mellitus, Mendelian randomization, causal inference, European descent