Pro-inflammatory cytokines as emerging molecular determinants in cardiolaminopathies

Andrea Gerbino1, Cinzia Forleo2, Serena Milano1

  • 1Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari, Bari, Italy.

Insights

Mutations in the Lamin A/C gene (LMNA) trigger cardiac inflammation, evidenced by elevated granulocyte colony-stimulating factor (G-CSF) and interleukin-6 (IL-6). This finding offers new diagnostic and therapeutic avenues for LMNA-related cardiomyopathies.

Area of Science:

  • Cardiovascular Medicine
  • Genetics
  • Immunology

Background:

  • Mutations in the Lamin A/C gene (LMNA) are linked to cardiolaminopathies, causing heart dysfunction.
  • The precise role of cardiac inflammation in LMNA mutation-related heart remodeling remains unclear.

Purpose of the Study:

  • To investigate serum cytokine and chemokine profiles in patients with LMNA mutations.
  • To correlate specific inflammatory markers with the severity of cardiac phenotypes.

Main Methods:

  • Serum samples from 19 patients with pathogenic LMNA mutations and 11 healthy controls were analyzed.
  • Cytokine/chemokine levels were profiled using multiplex assays.
  • Expression of heat shock protein 70 (Hsp70) in serum exosomes was assessed.

Main Results:

  • All patients with LMNA mutations exhibited elevated granulocyte colony-stimulating factor (G-CSF) and interleukin-6 (IL-6).
  • Increased levels of IL-1Ra, IL-1β, IL-4, IL-5, IL-8, and GM-CSF were observed in patients with more severe disease.
  • Elevated Hsp70 expression in serum exosomes correlated with the most severe phenotypes.

Conclusions:

  • Specific inflammatory profiles are associated with LMNA cardiomyopathies.
  • Identifying these inflammatory signatures may provide novel diagnostic and prognostic tools.
  • Targeting myocardial inflammation could be a therapeutic strategy for LMNA-related heart disease.

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