ID 64123
JaLCDOI
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Author
Zhang, Quan Department of Cardiovascular Medicine, Affiliated Hospital of Gansu Medical College
Yang, Lixia Department of Cardiovascular Medicine, Affiliated Hospital of Gansu Medical College
Wan, Guozhen Department of Cardiovascular Medicine, Affiliated Hospital of Gansu Medical College
Zhang, Xiaoqiang Department of Cardiovascular Medicine, Affiliated Hospital of Gansu Medical College
Wang, Ying Department of Cardiovascular Medicine, Affiliated Hospital of Gansu Medical College
Zhao, Guannan Department of Dermatological, Pingliang Traditional Chinese Medicine Hospital
Abstract
The diagnostic value of microRNA-377 (miR-377) in patients with acute coronary syndrome (ACS) and explored miR-377’s potential mechanisms. We performed an qRT-PCR to assess serum miR-377 levels in ACS patients and coronary artery ligation rat models. The diagnostic value of miR-377 was evaluated by determining the ROC curve. An ELISA assay was conducted to detect the model rat endothelial damage markers von Willebrand factor (vWF) and heart-type fatty acid binding protein (H-FABP), and proinflammatory cytokines TNF-α, IL-6, and IL-1β. The serum miR-377 level was elevated in the ACS patients and significantly increased in the ACS rats. MiR-377 has a high diagnostic value in ACS patients, with a 0.844 ROC, 76.47% specificity, and 87.10% sensitivity. MiR-377 was positively correlated with the expressions of vWF, H-FABP, cTnI, TNF-α, IL-6, and IL-1β. In ACS rats, reducing the expression of miR-377 significantly inhibited the increases in vWF, H-FABP, TNF-α, IL-6, and IL-1β. An elevated miR-377 level can be used as a diagnostic marker in patients with ACS. A reduction of miR-377 may alleviate ACS by improving myocardial damage such as endothelial injury and the inflammatory response.
Keywords
microRNA-377
acute coronary syndrome
diagnosis
endothelial injury
inflammatory
Amo Type
Original Article
Publication Title
Acta Medica Okayama
Published Date
2022-12
Volume
volume76
Issue
issue6
Publisher
Okayama University Medical School
Start Page
723
End Page
730
ISSN
0386-300X
NCID
AA00508441
Content Type
Journal Article
language
English
Copyright Holders
Copyright Ⓒ 2022 by Okayama University Medical School
File Version
publisher
Refereed
True
PubMed ID
Web of Science KeyUT