Gut Microbial Changes Associated With Obesity in Youth With Type 1 Diabetes

Author:

Ismail Heba M1ORCID,Perera Dimuthu2,Mandal Rabindra1,DiMeglio Linda A1,Evans-Molina Carmella1ORCID,Hannon Tamara1,Petrosino Joseph2,Javornik Cregeen Sara2,Schmidt Nathan W1

Affiliation:

1. Department of Pediatrics, Indiana University School of Medicine , Indianapolis, IN 46202 , USA

2. Department of Molecular Virology and Microbiology, Baylor College of Medicine , Houston, TX 77030 , USA

Abstract

Abstract Context Obesity is prevalent in type 1 diabetes (T1D) and is problematic with higher risk for diabetes complications. It is unknown to what extent gut microbiome changes are associated with obesity and T1D. Objective This work aimed to describe the gut microbiome and microbial metabolite changes associated with obesity in T1D. We hypothesized statistically significant gut microbial and metabolite differences in lean T1D youth (body mass index [BMI]: 5%-<85%) vs those with obesity (BMI: ≥95%). Methods We analyzed stool samples for gut microbial (using metagenomic shotgun sequencing) and short-chain fatty acid (SCFA) differences in lean (n = 27) and obese (n = 21) T1D youth in a pilot study. The mean ± SD age was 15.3 ± 2.2 years, glycated hemoglobin A1c 7.8 ± 1.3%, diabetes duration 5.1 ± 4.4 years, 42.0% female, and 94.0% were White. Results Bacterial community composition showed between sample diversity differences (β-diversity) by BMI group (P = .013). There was a higher ratio of Prevotella to Bacteroides in the obese group (P = .0058). There was a differential distribution of significantly abundant taxa in either the lean or obese groups, including increased relative abundance of Prevotella copri, among other taxa in the obese group. Functional profiling showed an upregulation of branched-chain amino acid (BCAA) biosynthesis in the obese group and upregulation of BCAA degradation, tyrosine metabolism, and secondary bile acid biosynthesis in the lean group. Stool SCFAs were higher in the obese vs the lean group (P < .05 for all). Conclusion Our findings identify a gut microbiome and microbial metabolite signature associated with obesity in T1D. These findings could help identify gut microbiome–targeted therapies to manage obesity in T1D.

Funder

National Institutes of Health

National Center for Advancing Translational Sciences

Indiana University Health Values Fund

Indiana Clinical and Translational Sciences Institute

Clinical and Translational Sciences Award

Pilot and Feasibility Grant

Indiana Center for Diabetes and Metabolic Diseases

National Institute of Diabetes and Digestive and Kidney Diseases

Doris Duke Charitable Foundation

Retain Clinical Scientists Collaborative Grant Program

The John Templeton Foundation

Publisher

The Endocrine Society

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