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Cardiovasc Diabetol ; 23(1): 268, 2024 Jul 22.
Artigo em Inglês | MEDLINE | ID: mdl-39039512

RESUMO

Ischemia with non-obstructive coronary artery (INOCA) is a common cause of hospital admissions, leading to negative outcomes and reduced quality of life. Central to its pathophysiology is endothelial dysfunction, which contributes to myocardial ischemia despite the absence of significant coronary artery blockage. Addressing endothelial dysfunction is essential in managing INOCA to alleviate symptoms and prevent cardiovascular events. Recent studies have identified diabetes mellitus (DM) as a significant factor exacerbating INOCA complications by promoting endothelial impairment and coronary microvascular dysfunction. MicroRNAs (miRNAs) have emerged as potential biomarkers and therapeutic targets in various biological processes, including endothelial dysfunction and cardiovascular diseases. However, research on miRNA biomarkers in INOCA patients is sparse. In this study, we examined a panel of circulating miRNAs involved in the regulation of endothelial function in INOCA patients with and without DM. We analyzed miRNA expression using RT-qPCR in a cohort of consecutive INOCA patients undergoing percutaneous coronary intervention. We detected a significant dysregulation of miR-363-5p and miR-92a-3p in INOCA patients with DM compared to those without DM, indicating their role as biomarkers for predicting and monitoring endothelial dysfunction in INOCA patients with DM.


Assuntos
MicroRNA Circulante , Doença da Artéria Coronariana , MicroRNAs , Humanos , Masculino , MicroRNAs/genética , MicroRNAs/sangue , MicroRNAs/metabolismo , Feminino , Pessoa de Meia-Idade , Idoso , Doença da Artéria Coronariana/genética , Doença da Artéria Coronariana/sangue , MicroRNA Circulante/sangue , MicroRNA Circulante/genética , Diabetes Mellitus/genética , Diabetes Mellitus/diagnóstico , Diabetes Mellitus/sangue , Intervenção Coronária Percutânea/efeitos adversos , Endotélio Vascular/metabolismo , Endotélio Vascular/fisiopatologia , Marcadores Genéticos , Células Endoteliais/metabolismo , Estudos de Casos e Controles
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