» Articles » PMID: 39090986

Exploring the Causal Connection: Insights into Diabetic Nephropathy and Gut Microbiota from Whole-genome Sequencing Databases

Overview
Journal Ren Fail
Publisher Informa Healthcare
Date 2024 Aug 2
PMID 39090986
Authors
Affiliations
Soon will be listed here.
Abstract

Over recent years, the prevalence of diabetes has been on the rise, paralleling improvements in living standards. Diabetic nephropathy (DN), a prevalent complication of diabetes, has also exhibited a growing incidence. While some clinical studies and reviews have hinted at a link between diabetic nephropathy and gut microbiota (GM), the nature of this connection, specifically its causative nature, remains uncertain. Investigating the causal relationship between diabetic nephropathy and gut microbiota holds the promise of aiding in disease screening and identifying novel biomarkers. In this study, we employed a two-sample Mendelian randomization analysis. Our dataset encompassed 4,111 DN patients from the GWAS database, juxtaposed with 308,539 members forming a control group. The aim was to pinpoint specific categories within the vast spectrum of the 211 known gut microbiota types that may have a direct causal relationship with diabetic nephropathy. Rigorous measures, including extensive heterogeneity and sensitivity analyses, were implemented to mitigate the influence of confounding variables on our experimental outcomes. Ultimately, our comprehensive analysis revealed 15 distinct categories of gut microbiota that exhibit a causal association with diabetic nephropathy. In summary, the phyla Bacteroidota and Verrucomicrobiae, the families Peptostreptococcaceae and Veillonellaceae, the genus Akkermansia, and the species Catenibacterium, Lachnoclostridium, Parasutterella, along with the orders Bacteroidales and Verrucomicrobiales, and the class Bacteroidetes were identified as correlates of increased risk for DN. Conversely, the family Victivallaceae, the species Eubacterium coprostanoligenes, and the Clostridium sensu stricto 1 group were found to be associated with a protective effect against the development of DN.These findings not only provide valuable insights but also open up novel avenues for clinical research, offering fresh directions for potential treatments.

Citing Articles

Integrative Roles of Functional Foods, Microbiotics, Nutrigenetics, and Nutrigenomics in Managing Type 2 Diabetes and Obesity.

Lam H, Lin S, Nguyen D, Chen C, Su C, Fang T Nutrients. 2025; 17(4).

PMID: 40004938 PMC: 11858703. DOI: 10.3390/nu17040608.


A practical guide for nephrologist peer reviewers: understanding and appraising Mendelian randomization studies.

Qing J, Li Y, Soliman K, Cheungpasitporn W Ren Fail. 2025; 47(1):2445763.

PMID: 39806780 PMC: 11734392. DOI: 10.1080/0886022X.2024.2445763.


Exploring the relationship between gut microbiota, immune characteristics, and female genital tract polyps using genetic evidence.

Jia R, Fu Y, Xue M, Zhou C, Jin J Medicine (Baltimore). 2024; 103(49):e40833.

PMID: 39654186 PMC: 11630997. DOI: 10.1097/MD.0000000000040833.

References
1.
Iatcu C, Steen A, Covasa M . Gut Microbiota and Complications of Type-2 Diabetes. Nutrients. 2022; 14(1). PMC: 8747253. DOI: 10.3390/nu14010166. View

2.
Ni Y, Zheng L, Nan S, Ke L, Fu Z, Jin J . Enterorenal crosstalks in diabetic nephropathy and novel therapeutics targeting the gut microbiota. Acta Biochim Biophys Sin (Shanghai). 2022; 54(10):1406-1420. PMC: 9827797. DOI: 10.3724/abbs.2022140. View

3.
Lee C, Chae S, Jo S, Jerng U, Bae S . The Relationship between the Gut Microbiome and Metformin as a Key for Treating Type 2 Diabetes Mellitus. Int J Mol Sci. 2021; 22(7). PMC: 8037857. DOI: 10.3390/ijms22073566. View

4.
Fang Q, Liu N, Zheng B, Guo F, Zeng X, Huang X . Roles of Gut Microbial Metabolites in Diabetic Kidney Disease. Front Endocrinol (Lausanne). 2021; 12:636175. PMC: 8173181. DOI: 10.3389/fendo.2021.636175. View

5.
Kim C, Park J, Kim M . Gut microbiota-derived short-chain Fatty acids, T cells, and inflammation. Immune Netw. 2015; 14(6):277-88. PMC: 4275385. DOI: 10.4110/in.2014.14.6.277. View