Coronary disease & ACSCohort study

Gut microbiota-derived imidazole propionate predicts cardiometabolic risk in patients with coronary artery disease

Eur Heart JPublished

  • Prospective cohort study
  • multiple independent cohorts
  • multivariable Cox models

Authors' conclusion

Gut microbiota-derived ImP predicted MACE in patients with CAD independently of traditional risk factors

Study context

Population
Patients with coronary artery disease (CAD): Acute coronary syndrome (ACS) (Swiss ACS, Swiss CMR, German ACS cohorts) and chronic coronary syndrome (German chronic coronary syndrome (CCS) cohort)independent prospective cohorts
Exposure
Circulating imidazole propionate levels and major adverse cardiovascular events (MACE)
Outcome
MACE:
  • First occurrence of death
  • Non-fatal MI
  • Non-fatal stroke after admission

Main finding

As reported in the abstract

MACE
ImPHazard ratio (95% CI)P value
Swiss ACS cohort; per log2 increase; adjusted for established risk factors
1.22(1.10–1.35)
P < 0.001
German ACS cohort; adjusted
2.34(1.46–3.76)
P < 0.001
German CCS cohort; adjusted
1.32(1.13–1.53)
P < 0.001

Per log2 increase, as printed

Observational data: associations, not effects.

Further findings

Mortality

ComparisonHR (95% CI)P value
ImP · Swiss ACS cohort; adjusted for established risk factors1.34 (1.17–1.54)P < 0.001
ImP · German ACS cohort; adjusted for established risk factors2.38 (1.48–3.82)P < 0.001
ImP · German CCS cohort; adjusted for established risk factors1.50 (1.14–1.98)P = 0.004

Predictive value beyond trimethylamine N-oxide

ComparisonHR (95% CI)P value
Imidazole propionate · Swiss ACS cohort1.30 (1.05–1.61)P = 0.014
Imidazole propionate · German CCS cohort1.31 (1.12–1.53)P = 0.001

Original publication

Gut microbiota-derived imidazole propionate predicts cardiometabolic risk in patients with coronary artery disease. Eur Heart J. Published 30 August 2025. doi:10.1093/eurheartj/ehaf661

Summarised from the published abstract; every number is checked against it