Expanding landscape of coronary microvascular disease in co-morbid conditions: Metabolic disease and beyond

Patricia E McCallinhart1, Alejandro R Chade2, Shawn B Bender3

  • 1Center for Cardiovascular Research, The Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, United States of America.

Insights

Coronary microvascular disease (CMD) impairs blood flow early in heart failure, predicting cardiac events in metabolic disease. This review covers CMD mechanisms in metabolic and other conditions using animal models and clinical data.

Area of Science:

  • Cardiovascular Science
  • Pathophysiology
  • Translational Medicine

Background:

  • Coronary microvascular disease (CMD) and impaired coronary blood flow control are early defects in heart failure pathogenesis within cardiometabolic conditions.
  • CMD precedes atherosclerosis and is an independent predictor of cardiac morbidity and mortality in patients with obesity and metabolic disease.
  • CMD involves functional, structural, and mechanical impairments reducing coronary blood flow in metabolic disease and other conditions like transplant, autoimmune disorders, cardiotoxicity, and remote injury.

Purpose of the Study:

  • To review the current understanding of CMD in metabolic and comorbid conditions.
  • To synthesize mechanistic data from preclinical animal models with available clinical evidence.
  • To identify knowledge gaps and future research opportunities in CMD.

Main Methods:

  • Review of contemporary literature on Coronary Microvascular Disease (CMD).
  • Focus on mechanistic data from preclinical small- and large-animal models.
  • Integration of available clinical evidence, acknowledging limitations in human studies.

Main Results:

  • CMD is a significant early defect in heart failure associated with cardiometabolic conditions.
  • CMD predicts cardiac events and is linked to obesity and metabolic disease.
  • Mechanisms of CMD are explored across metabolic, transplant, autoimmune, cardiotoxicity, and remote injury contexts.

Conclusions:

  • CMD is a critical factor in heart failure development across various conditions.
  • Preclinical models provide valuable mechanistic insights into CMD.
  • Further research is needed to bridge the gap between animal models and human clinical applications for CMD.

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