Sex and gender differences in myocarditis and dilated cardiomyopathy

Curr Probl Cardiol. 2013 Jan;38(1):7-46. doi: 10.1016/j.cpcardiol.2012.07.003.

Abstract

Heart failure due to nonischemic dilated cardiomyopathy (DCM) contributes significantly to the global burden of cardiovascular disease. Myocarditis is, in turn, a major cause of acute DCM in both men and women. However, recent clinical and experimental evidence suggests that the pathogenesis and prognosis of DCM differ between the sexes. This seminar provides a contemporary perspective on the immune mediators of myocarditis, including interdependent elements of the innate and adaptive immune response. The heart's acute response to injury is influenced by sex hormones that appear to determine the subsequent risk of chronic DCM. Preliminary data suggest additional genetic variations may account for some of the differences in epidemiology, left ventricular recovery, and survival between men and women. We highlight the gaps in our knowledge regarding the management of women with acute DCM and discuss emerging therapies, including bromocriptine for the treatment of peripartum cardiomyopathy.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Cardiomyopathy, Dilated* / genetics
  • Cardiomyopathy, Dilated* / immunology
  • Cardiomyopathy, Dilated* / metabolism
  • Cardiomyopathy, Dilated* / mortality
  • Cardiomyopathy, Dilated* / pathology
  • Cardiomyopathy, Dilated* / physiopathology
  • Cardiomyopathy, Dilated* / therapy
  • Female
  • Genetic Predisposition to Disease
  • Gonadal Steroid Hormones / metabolism
  • Health Status Disparities
  • Healthcare Disparities
  • Humans
  • Inflammation Mediators / metabolism
  • Male
  • Myocarditis* / genetics
  • Myocarditis* / immunology
  • Myocarditis* / metabolism
  • Myocarditis* / mortality
  • Myocarditis* / pathology
  • Myocarditis* / physiopathology
  • Myocarditis* / therapy
  • Myocardium* / immunology
  • Myocardium* / metabolism
  • Myocardium* / pathology
  • Recovery of Function
  • Risk Factors
  • Sex Factors
  • Treatment Outcome
  • Ventricular Function, Left

Substances

  • Gonadal Steroid Hormones
  • Inflammation Mediators