Diabetic Cardiomyopathy: From Mechanism to Management in a Nutshell

Endocr Metab Immune Disord Drug Targets. 2021;21(2):268-281. doi: 10.2174/1871530320666200731174724.

Abstract

Diabetic cardiomyopathy (DCM) is a significant complication of diabetes mellitus characterized by gradually failing heart with detrimental cardiac remodelings, such as fibrosis and diastolic and systolic dysfunction, which is not directly attributable to coronary artery disease. Insulin resistance and resulting hyperglycemia is the main trigger involved in the initiation of diabetic cardiomyopathy. There is a constellation of many pathophysiological events, such as lipotoxicity, oxidative stress, inflammation, inappropriate activation of the renin-angiotensin-aldosterone system, dysfunctional immune modulation promoting increased rate of cardiac cell injury, apoptosis, and necrosis, which ultimately culminates into interstitial fibrosis, cardiac stiffness, diastolic dysfunction, initially, and later systolic dysfunction too. These events finally lead to clinical heart failure of DCM. Herein, The pathophysiology of DCM is briefly discussed. Furthermore, potential therapeutic strategies currently used for DCM are also briefly mentioned.

Keywords: Diabetic cardiomyopathy; diabetes mellitus; heart failure; hyperglycemia; insulin resistance; pathophysiology.

Publication types

  • Review

MeSH terms

  • Animals
  • Diabetes Mellitus / drug therapy
  • Diabetes Mellitus / epidemiology
  • Diabetes Mellitus / metabolism*
  • Diabetic Cardiomyopathies / drug therapy
  • Diabetic Cardiomyopathies / epidemiology
  • Diabetic Cardiomyopathies / metabolism*
  • Disease Management*
  • Heart Failure / drug therapy
  • Heart Failure / epidemiology
  • Heart Failure / metabolism
  • Humans
  • Hyperglycemia / drug therapy
  • Hyperglycemia / epidemiology
  • Hyperglycemia / metabolism
  • Hypoglycemic Agents / pharmacology
  • Hypoglycemic Agents / therapeutic use
  • Insulin Resistance / physiology*
  • Myocardium / metabolism*
  • Oxidative Stress / drug effects
  • Oxidative Stress / physiology
  • Renin-Angiotensin System / drug effects
  • Renin-Angiotensin System / physiology

Substances

  • Hypoglycemic Agents