Gut microbiota dysbiosis in stable coronary artery disease combined with type 2 diabetes mellitus influences cardiovascular prognosis

Nutr Metab Cardiovasc Dis. 2021 May 6;31(5):1454-1466. doi: 10.1016/j.numecd.2021.01.007. Epub 2021 Jan 21.

Abstract

Background and aims: Host-microbiota interactions involving metabolic pathways have been linked to the pathogenesis of atherosclerotic disease and type 2 diabetes. As stable coronary artery disease (SCAD) patients combined with type 2 diabetes have significantly increased risk for cardiac event, we focused on elucidating the role of microbiota affecting cardiometabolic disease development.

Methods and results: We used multi-omics analyses (metagenomics and metabolomics) of fecal and serum samples from a prospective cohort including stable coronary artery disease combined with diabetes mellitus (SCAD + T2DM, n = 38), SCAD (n = 71), and healthy control (HC, n = 55). We linked microbiome features to disease severity in a three-pronged association analysis and identified prognostic bacterial biomarkers. We identified that bacterial and metabolic signatures varied significantly between SCAD and SCAD + T2DM groups. SCAD + T2DM individuals were characterized by increased levels of aromatic amino acids and carbohydrates, which correlate with a gut microbiome with enriched biosynthetic potential. Our study also addressed how metformin may confound gut dysbiosis and increase the potential for nitrogen metabolism. In addition, we found that specific bacterial taxa Ruminococcus torques [HR: 2.363 (08-4.56), P = 0.03] was predictive of cardiac survival outcomes.

Conclusion: Overall, our study identified relationships between features of the gut microbiota (GM) and circulating metabolites, providing a new direction for future studies aiming to understand the host-GM interplay in atherosclerotic cardiovascular pathogenesis.

Keywords: Cardiovascular prognosis; Metabolomics; Metagenomics; Multi-omics analysis; Stable coronary artery disease; Type 2 diabetes mellitus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Bacteria / drug effects
  • Bacteria / growth & development
  • Bacteria / metabolism*
  • Biomarkers / blood
  • Case-Control Studies
  • Clostridiales / growth & development
  • Clostridiales / metabolism
  • Coronary Artery Disease / blood
  • Coronary Artery Disease / diagnosis
  • Coronary Artery Disease / microbiology*
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / diagnosis
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diabetes Mellitus, Type 2 / microbiology*
  • Dysbiosis
  • Female
  • Gastrointestinal Microbiome* / drug effects
  • Host-Pathogen Interactions
  • Humans
  • Hypoglycemic Agents / therapeutic use
  • Intestines / microbiology*
  • Male
  • Metabolomics
  • Metagenomics
  • Metformin / therapeutic use
  • Middle Aged
  • Prognosis
  • Prospective Studies

Substances

  • Biomarkers
  • Hypoglycemic Agents
  • Metformin

Supplementary concepts

  • Ruminococcus torques