This study aimed to identify microbial signatures that contribute to the shared etiologies between chronic heart failure (CHF), type 2 diabetes, and chronic kidney disease. The serum levels of 151 microbial metabolites were measured in 260 individuals from the Risk Evaluation and Management of heart failure cohort, and it was found that those metabolites varied by an order of 10
5
fold. Out of 96 metabolites associated with the three cardiometabolic diseases, most were validated in two geographically independent cohorts. In all three cohorts, 16 metabolites including imidazole propionate (ImP) consistently showed significant differences. Notably, baseline ImP levels were three times higher in the Chinese compared with the Swedish cohorts and increased by 1.1–1.6 fold with each additional CHF comorbidity in the Chinese population. Cellular experiments further supported a causal link between ImP and distinct CHF relevant phenotypes. Additionally, key microbial metabolite‐based risk scores were superior in CHF prognosis than the traditional Framingham or Get with the Guidelines‐Heart Failure risk scores. Interactive visualization of these specific metabolite‐disease links is available on our omics data server (
https://omicsdata.org/Apps/REM‐HF/
).
Synopsis
Targeted metabolomics profiling and cellular experiments revealed that many microbially associated metabolites may mediate the pathogenesis of chronic heart failure (CHF), as well as its related comorbidities including type 2 diabetes and chronic kidney diseases.
Alteration of microbially associated metabolites was...

Microbial metabolites in chronic heart failure and its common comorbidities

10.15252/emmm.202216928