Diabetic Cardiomyopathy: An Update of Mechanisms Contributing to This Clinical Entity

Guanghong Jia1, Michael A Hill1, James R Sowers2

  • 1From the Diabetes and Cardiovascular Research Center (G.J., J.R.S.) and Department of Medical Pharmacology and Physiology (M.A.H., J.R.S.), University of Missouri School of Medicine, Columbia; Dalton Cardiovascular Research Center, University of Missouri, Columbia (M.A.H., J.R.S.); and Research Service, Truman Memorial Veterans Hospital, Columbia, MO (G.J., J.R.S.).

Circulation Research
|February 17, 2018
PubMed

Insights

Diabetic cardiomyopathy, a growing concern linked to diabetes mellitus, causes heart dysfunction through fibrosis and remodeling. Understanding its molecular causes is key to developing new treatments.

Area of Science:

  • Cardiology
  • Endocrinology
  • Molecular Medicine

Background:

  • Heart failure is rising, particularly in patients with diabetes mellitus, who face worse outcomes.
  • Diabetic cardiomyopathy is characterized by myocardial dysfunction independent of traditional cardiovascular risk factors.
  • Its prevalence parallels the increasing rates of diabetes mellitus.

Purpose of the Study:

  • To review the instigators of diabetic cardiomyopathy.
  • To provide a contemporary view of its development and progression.
  • To discuss mechanistically based prevention and treatment strategies.

Main Methods:

  • Review of current literature on diabetic cardiomyopathy.
  • Analysis of molecular and cellular mechanisms.
  • Synthesis of pathophysiological pathways.

Main Results:

  • Diabetic cardiomyopathy involves myocardial fibrosis, diastolic and systolic dysfunction.
  • Key implicated mechanisms include impaired insulin signaling, mitochondrial dysfunction, oxidative stress, and inflammation.
  • Molecular pathways affected include AMP-activated protein kinase, peroxisome proliferator-activated receptors, and O-linked N-acetylglucosamine.

Conclusions:

  • Diabetic cardiomyopathy is a complex condition with multifactorial origins.
  • Targeting specific molecular and metabolic pathways offers potential for therapeutic intervention.
  • Further research is needed to translate mechanistic insights into effective clinical strategies.

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