MicroRNAs and Sepsis-Induced Cardiac Dysfunction: A Systematic Review

Alice Chiara Manetti1, Aniello Maiese1,2, Marco Di Paolo1

  • 1Department of Surgical Pathology, Medical, Molecular and Critical Area, Institute of Legal Medicine, University of Pisa, 56126 Pisa (PI), Italy.

Insights

MicroRNAs (miRNAs) play a key role in sepsis-induced heart dysfunction. This review highlights 77 miRNAs involved, suggesting their potential as early biomarkers and therapeutic targets for cardiac damage.

Area of Science:

  • Biomedical Science
  • Molecular Biology
  • Cardiology

Background:

  • Sepsis triggers systemic inflammation, frequently leading to heart dysfunction and failure, a major cause of mortality.
  • MicroRNAs (miRNAs) are epigenetic regulators of gene expression, with distinct expression patterns in various conditions.
  • Altered miRNA expression in sepsis suggests their potential as diagnostic biomarkers for cardiac involvement.

Purpose of the Study:

  • To review and summarize the current knowledge on the role of miRNAs in sepsis-induced cardiac dysfunction.
  • To identify specific miRNAs implicated in the inflammatory and functional changes of the heart during sepsis.
  • To explore the potential of miRNAs as early diagnostic biomarkers and therapeutic targets for sepsis-related heart injury.

Main Methods:

  • A narrative literature review was conducted.
  • Relevant studies on miRNAs, sepsis, and cardiac dysfunction were systematically searched and analyzed.
  • Findings were synthesized to provide a comprehensive overview of the current understanding.

Main Results:

  • At least 77 different miRNAs have been identified as being involved in cardiac inflammation and dysfunction during sepsis.
  • miRNA expression profiles differ significantly in sepsis, indicating their condition-specific regulatory roles.
  • The identified miRNAs are implicated in various biological pathways affecting cardiac function.

Conclusions:

  • MicroRNAs show significant promise as potential early diagnostic biomarkers for sepsis-induced cardiac dysfunction.
  • Targeting specific miRNAs could offer novel therapeutic strategies for preventing and treating myocardial injury in sepsis.
  • Further research is essential to elucidate the complex roles of miRNAs in sepsis pathophysiology and their clinical applications.