Key result
Obesity drives coronary microvascular dysfunction via adipokine-mediated inflammation and impaired nitric oxide vasodilation.
This review synthesizes basic and clinical evidence linking obesity to coronary microvascular dysfunction via chronic adipokine-driven inflammation, endothelial impairment, and altered vasomotor regulation, highlighting current diagnostic and therapeutic challenges.
Answers are grounded in this paper and cite their sources.
Does not support immediate CMD management changes in obesity; leaves open validation of adipokine-targeted therapies in prospective trials.
Obesity related coronary microvascular disease is a medical entity which is not yet fully elucidated. The pathophysiological basis of coronary microcirculatory dysfunction consists of a heterogeneous group of disorders with individual morphologic/functional/clinical presentation and prognosis. Coronary microcirculatory changes include mechanisms connected with vascular dysfunction, as well as extravascular and vasostructural changes in responses to neural, mechanical, and metabolic factors. Cardiometabolic changes that include obesity, dyslipidemia, diabetes mellitus type II, and hypertension are associated with atherosclerosis of epicardial coronary arteries and/or microvascular coronary dysfunction, with incompletely understood underlying mechanisms. In obesity, microvascular disease is mediated via adipokines/cytokines causing chronic, subclinical inflammation with (a) reduced NO-mediated dilatation, (b) changed endothelial- and smooth muscle-dependent vasoregulating mechanisms, (c) altered vasomotor control with increased sympathetic activity, and (d) obesity related hypertension with cardiomyocytes hypertrophy and impaired cardiac vascular adaptation to metabolic needs. From a clinical point of view it can present itself in acute or chronic form with different prognosis, as a practice problem for real-life diagnosis and treatment.
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Selthofer-Relatić et al. (2016) conducted a review in Obesity-related coronary microvascular dysfunction (CMD). Obesity was evaluated. Obesity promotes coronary microvascular dysfunction via adipokine-mediated chronic inflammation, reduced nitric oxide-mediated dilation, and altered vasomotor control.
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