Gut microbiome shifts in chronic systolic heart failure are associated with disease severity and clinical improvement

Abstract The contribution of the gut microbiome to chronic heart failure (HF) remains poorly defined. We performed integrated microbiome and host multi-omic profiling of adults with chronic systolic HF due to nonischemic cardiomyopathy ( n = 59) and healthy participants ( n = 50), including longitudinal sampling in some cases. Here we show that patients with HF have depletion of anti-inflammatory Bifidobacterium and reduced short-chain fatty acid biosynthetic potential, alongside altered microbiome–immune system interactions. Longitudinal analysis revealed that higher Bifidobacterium abundance was associated with clinical improvement. Multi-omic integration prioritized indole-3-propionic acid (IPA), a gut metabolite with cardioprotective properties, as a candidate mechanistic link. We confirmed that Bifidobacterium species can produce IPA in vitro and circulating IPA levels were associated with milder HF severity. Together, these findings define gut microbiome alterations in chronic systolic HF, identify candidate microbiome biomarkers of disease severity and trajectory, and suggest microbiome-derived metabolites as potential therapeutic targets.

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Publication Details

Journal
Nature Cardiovascular Research
Published
2026-09-24
DOI
https://doi.org/10.1038/s44161-026-00854-y
Primary Topic
Gut microbiota and health
Type
article
Field-Weighted Citation Impact
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article

Gut microbiome shifts in chronic systolic heart failure are associated with disease severity and clinical improvement

Kiran K. Khush, Sophia Miryam Schüssler‐Fiorenza Rose, Michael Snyder, Paul A. Heidenreich et al.
Nature Cardiovascular Research
Gut microbiota and health
article

Gut microbiome shifts in chronic systolic heart failure are associated with disease severity and clinical improvement

Kiran K. Khush, Sophia Miryam Schüssler‐Fiorenza Rose, Michael Snyder, Paul A. Heidenreich, Nasim Bararpour, W.H. Wilson Tang, Wenyu Zhou, Kerwyn Casey Huang, Heyjun Park, Monika Avina, Kévin Contrepois, Handuo Shi, Petra Mamic, Justin L. Sonnenburg, Masakazu Kotaka, Karim Sallam, Michael B. Fowler, Andrew W. Brooks
article en

Abstract

Abstract The contribution of the gut microbiome to chronic heart failure (HF) remains poorly defined. We performed integrated microbiome and host multi-omic profiling of adults with chronic systolic HF due to nonischemic cardiomyopathy ( n = 59) and healthy participants ( n = 50), including longitudinal sampling in some cases. Here we show that patients with HF have depletion of anti-inflammatory Bifidobacterium and reduced short-chain fatty acid biosynthetic potential, alongside altered microbiome–immune system interactions. Longitudinal analysis revealed that higher Bifidobacterium abundance was associated with clinical improvement. Multi-omic integration prioritized indole-3-propionic acid (IPA), a gut metabolite with cardioprotective properties, as a candidate mechanistic link. We confirmed that Bifidobacterium species can produce IPA in vitro and circulating IPA levels were associated with milder HF severity. Together, these findings define gut microbiome alterations in chronic systolic HF, identify candidate microbiome biomarkers of disease severity and trajectory, and suggest microbiome-derived metabolites as potential therapeutic targets.

Nature Cardiovascular Research
Cleveland Clinic (US), Johns Hopkins University (US), Cardiovascular Institute of the South (US), Cleveland Clinic Lerner College of Medicine (US), Chan Zuckerberg Initiative (United States) (US), Stanford Medicine (US), New Mexico VA Health Care System (US), Stanford Cardiovascular Institute (US), Stanford University (US)
Good health and well-being
Openalex Percentile: Top 19%
Gut microbiota and health
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