Prognosis value of galectin-3 in patients with dilated cardiomyopathy: a meta-analysis

PeerJ. 2024 Apr 23:12:e17201. doi: 10.7717/peerj.17201. eCollection 2024.

Abstract

Background: Accurate prediction and assessment of myocardial fibrosis (MF) and adverse cardiovascular events (MACEs) are crucial in patients with dilated cardiomyopathy (DCM). Several studies indicate that galectin-3 (gal-3) as a promising prognostic predictor in patients with DCM.

Methods: A comprehensive search was conducted in PubMed, EMBASE, the Cochrane Library, and Web of Science for relevant studies up to August 2023. The hazard ratios (HRs) of gal-3 for MACEs in DCM patients, and for MACEs in LGE(+) versus LGE(-) groups, were evaluated. Statistical analysis was performed using STATA SE 14.0 software.

Results: Seven studies, encompassing 945 patients, met the eligibility criteria. In DCM patients, abnormally elevated gal-3 levels were indicative of an increased MACEs risk (HR = 1.10, 95% CI [1.00-1.21], I2 = 65.7%, p = 0.008). Compared with the LGE(-) group, the level of gal-3 in LGE(+) group was higher (HR = 1.12, 95% CI [1.05-1.19], I2 = 31.4%, p = 0.233), and the combination of gal-3 and LGE significantly improved the prediction of MACEs. Sensitivity analysis confirmed the robustness of all results.

Conclusions: This study's findings suggest that elevated gal-3 levels significantly correlate with increased MACE risk in DCM, highlighting its potential as a biomarker. However, significant heterogeneity among studies necessitates further research to ascertain gal-3's predictive and diagnostic value in DCM prognosis, particularly in conjunction with LGE.

Prospero id: CRD42023471199.

Keywords: Cardiology; Galectin-3, dilated cardiomyopathies, MACEs, meta-analysis; Genetics.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers* / blood
  • Blood Proteins / analysis
  • Cardiomyopathy, Dilated* / blood
  • Cardiomyopathy, Dilated* / diagnosis
  • Cardiomyopathy, Dilated* / mortality
  • Fibrosis
  • Galectin 3* / blood
  • Galectins* / blood
  • Humans
  • Myocardium / metabolism
  • Myocardium / pathology
  • Prognosis

Substances

  • Galectin 3
  • Biomarkers
  • LGALS3 protein, human
  • Galectins
  • Blood Proteins

Grants and funding

The authors received no funding for this work.