# Sepsis-induced cardiomyopathy: mechanisms, epidemiology, diagnosis, and treatments

**Authors:** Fei Cao, Tao Yan, Chaoyue Liang, Ao Liu, Junyan Wang

PMC · DOI: 10.3389/fimmu.2026.1785463 · Frontiers in Immunology · 2026-03-11

## TL;DR

This paper reviews sepsis-induced cardiomyopathy, a dangerous heart condition caused by sepsis, covering its causes, how it's diagnosed, and treatment options.

## Contribution

The paper provides a comprehensive synthesis of mechanisms, epidemiology, diagnosis, and treatment of sepsis-induced cardiomyopathy.

## Key findings

- Sepsis-induced cardiomyopathy involves inflammation, oxidative stress, and mitochondrial dysfunction.
- Younger age, male sex, and pre-existing heart failure are key risk factors for SICM.
- Pharmacological and mechanical treatments are used, with emerging therapies targeting ferroptosis and mitochondria.

## Abstract

Sepsis-induced cardiomyopathy (SICM) is a life-threatening complication of sepsis characterized by reversible myocardial dysfunction. Its pathophysiology involves a complex interplay of inflammatory pathways, oxidative stress, mitochondrial dysfunction, and genetic factors, leading to impaired cardiac contractility, ventricular dilatation, and increased mortality. Epidemiologically, SICM exhibits demographic variations, with younger age, male sex, and pre-existing heart failure identified as key risk factors. Diagnostic approaches rely on a combination of biomarkers (e.g., troponins, NT-proBNP), advanced imaging techniques (e.g., speckle-tracking echocardiography), and clinical criteria, though standardized definitions remain elusive. Treatment strategies include pharmacological interventions (e.g., levosimendan, melatonin), mechanical circulatory support (e.g., VA-ECMO, Impella), and emerging therapies targeting ferroptosis or mitochondrial function. Historical perspectives highlight the evolution from recognizing SICM as a rare complication to its current status as a major contributor to sepsis mortality, while future directions emphasize personalized medicine, multi-omics integration, and targeted therapeutics. This review synthesizes current knowledge of SICM, identifies critical gaps, and proposes actionable research priorities to improve patient outcomes.

## Linked entities

- **Chemicals:** levosimendan (PubChem CID 3033825), melatonin (PubChem CID 896)
- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Diseases:** inflammatory (MESH:D007249), heart failure (MESH:D006333), sepsis (MESH:D018805), ventricular dilatation (MESH:C566255), mitochondrial dysfunction (MESH:D028361), SICM (MESH:D009202), impaired cardiac contractility (MESH:D006331)
- **Chemicals:** melatonin (MESH:D008550), levosimendan (MESH:D000077464)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13012987/full.md

## References

72 references — full list in the complete paper: https://tomesphere.com/paper/PMC13012987/full.md

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Source: https://tomesphere.com/paper/PMC13012987