Gut microbiota and metabolic profiles in adults with unclassified diabetes: a cross-sectional study

Front Endocrinol (Lausanne). 2024 Nov 11:15:1440984. doi: 10.3389/fendo.2024.1440984. eCollection 2024.

Abstract

Aims: Our study, employing a multi-omics approach, aimed to delineate the distinct gut microbiota and metabolic characteristics in individuals under 30 with unclassified diabetes, thus shedding light on the underlying pathophysiological mechanisms.

Methods: This age- and sex-matched case-control study involved 18 patients with unclassified diabetes, 18 patients with classic type 1 diabetes, 13 patients with type 2 diabetes, and 18 healthy individuals. Metagenomics facilitated the profiling of the gut microbiota, while untargeted liquid chromatography-mass spectrometry was used to quantify the serum lipids and metabolites.

Results: Our findings revealed a unique gut microbiota composition in unclassified diabetes patients, marked by a depletion of Butyrivibrio proteoclasticus and Clostridium and an increase in Ruminococcus torques and Lachnospiraceae bacterium 8_1_57FAA. Comparative analysis identified the combined marker panel of five bacterial species, seven serum biomarkers, and three clinical parameters could differentiate patients with UDM from HCs with an AUC of 0.94 (95% CI 0.85-1). Notably, the gut microbiota structure of patients with unclassified diabetes resembled that of type 2 diabetes patients, especially regarding disrupted lipid and branched-chain amino acid metabolism.

Conclusions: Despite sharing certain metabolic features with type 2 diabetes, unclassified diabetes presents unique features. The distinct microbiota and metabolites in unclassified diabetes patients suggest a significant role in modulating glucose, lipid, and amino acid metabolism, potentially influencing disease progression. Further longitudinal studies are essential to explore therapeutic strategies targeting the gut microbiota and metabolites to modify the disease trajectory.

Keywords: correlation; diabetes mellitus; gut microbiome; metabolites analysis; metagenome.

MeSH terms

  • Adult
  • Biomarkers / blood
  • Case-Control Studies
  • Cross-Sectional Studies
  • Diabetes Mellitus, Type 1 / blood
  • Diabetes Mellitus, Type 1 / metabolism
  • Diabetes Mellitus, Type 1 / microbiology
  • Diabetes Mellitus, Type 2* / blood
  • Diabetes Mellitus, Type 2* / metabolism
  • Diabetes Mellitus, Type 2* / microbiology
  • Female
  • Gastrointestinal Microbiome* / physiology
  • Humans
  • Male
  • Metabolome*
  • Young Adult

Substances

  • Biomarkers

Grants and funding

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This study was supported by National Natural Science Foundation of China (82070864, 82470886), Shanghai Special Project “Science and Technology Innovation Action Plan” Medical Innovation Research ( 22Y11904800), and National Key R and D Program of China (2023YFC2506000, 2023YFC2506001).