New Biomarkers in the Diagnosis and Prognosis of Dilated Cardiomyopathy: Pro-Resolving Lipids and miRNAs

Rafael I Jaén1,2, Sergio Sánchez-García1,2, María Fernández-Velasco2,3

  • 1Department of Metabolism and Cell Signaling, Biomedical Research Institute "Sols-Morreale" CSIC-UAM, 28029 Madrid, Spain.

Cells
|December 10, 2025
PubMed

Insights

New biomarkers, including specific lipid mediators and circulating microRNAs, show promise for improving the diagnosis and prognosis of dilated cardiomyopathy (DCM). These findings could lead to better patient stratification and personalized treatments for heart failure.

Area of Science:

  • Cardiovascular Research
  • Biomarker Discovery
  • Molecular Medicine

Background:

  • Dilated cardiomyopathy (DCM) is a leading cause of heart failure with challenging diagnosis and prognosis due to non-specific biomarkers.
  • Inflammation is a key factor in DCM pathogenesis, necessitating the identification of novel inflammatory markers.

Purpose of the Study:

  • To investigate the potential of specific pro-resolving lipid mediators (SPMs) and circulating microRNAs (miRNAs) as novel biomarkers for DCM.
  • To assess the utility of these biomarkers, individually and in combination, for improving patient stratification and prognosis.

Main Methods:

  • Systemic inflammatory markers, SPMs (Lipoxin A4, Resolvin D1), and miRNA expression profiling were analyzed in a cohort of DCM patients and controls.
  • High-throughput array platform was used for comprehensive miRNA expression profiling.
  • ROC analysis and LASSO regression models were employed to evaluate biomarker performance.

Main Results:

  • Lipoxin A4 levels were significantly increased, while Resolvin D1 levels were decreased in DCM patients compared to controls.
  • Specific miRNAs (miR378-3p, miR486-5p, miR142-3p, miR328-3p) showed differential expression in DCM patients and were associated with inflammatory pathways.
  • A combination of miR142-3p and miR328-3p demonstrated promising prognostic value, though no correlation was found between miRNAs and SPMs.

Conclusions:

  • SPMs and specific circulating miRNAs represent novel potential biomarkers for DCM progression and prognosis.
  • Integrating inflammatory profiles with miRNA expression patterns offers a promising strategy for DCM patient stratification and personalized treatment.
  • A multi-parameter biomarker panel for DCM could enhance early diagnosis, improve prognosis, and guide clinical practice.

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