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
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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.
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Keywords | microRNA-377
acute coronary syndrome
diagnosis
endothelial injury
inflammatory
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Amo Type | Original Article
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Publication Title |
Acta Medica Okayama
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Published Date | 2022-12
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Volume | volume76
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Issue | issue6
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Publisher | Okayama University Medical School
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Start Page | 723
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End Page | 730
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ISSN | 0386-300X
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NCID | AA00508441
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Content Type |
Journal Article
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language |
English
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Copyright Holders | Copyright Ⓒ 2022 by Okayama University Medical School
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File Version | publisher
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Refereed |
True
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PubMed ID | |
Web of Science KeyUT |