Myostatin signaling is up-regulated in female patients with advanced heart failure

Int J Cardiol. 2017 Jul 1:238:37-42. doi: 10.1016/j.ijcard.2017.03.153. Epub 2017 Apr 4.

Abstract

Background: Myostatin, a negative regulator of skeletal muscle mass, is up-regulated in the myocardium of heart failure (HF) and increased myostatin is associated with weight loss in animal models with HF. Although there are disparities in pathophysiology and epidemiology between male and female patients with HF, it remains unclear whether there is gender difference in myostatin expression and whether it is associated with weight loss in HF patients.

Methods: Heart tissue samples were collected from patients with advanced heart failure (n=31, female n=5) as well as healthy control donors (n=14, female n=6). Expression levels of myostatin and its related proteins in the heart were evaluated by western blotting analysis.

Results: Body mass index was significantly lower in female HF patients than in male counterparts (20.0±4.2 in female vs 25.2±3.8 in male, p=0.04). In female HF patients, both mature myostatin and pSmad2 were significantly up-regulated by 1.9 fold (p=0.05) and 2.5 fold (p<0.01) respectively compared to female donors, while expression of pSmad2 was increased by 2.8 times in male HF patients compared to male healthy subjects, but that of myostatin was not. There was no significant difference in protein expression related to myostatin signaling between male and female patients.

Conclusion: In this study, myostatin and pSmad2 were significantly up-regulated in the failing heart of female patients, but not male patients, and female patients displayed lower body mass index. Enhanced myostatin signaling in female failing heart may causally contribute to pathogenesis of HF and cardiac cachexia.

Keywords: Chronic heart failure; Gender difference; Myocardium; Myostatin signaling.

MeSH terms

  • Adult
  • Aged
  • Female
  • Heart Failure / metabolism*
  • Heart Failure / pathology
  • Humans
  • Male
  • Middle Aged
  • Myostatin / biosynthesis*
  • Signal Transduction / physiology*
  • Smad2 Protein / biosynthesis*
  • Up-Regulation / physiology*

Substances

  • MSTN protein, human
  • Myostatin
  • SMAD2 protein, human
  • Smad2 Protein