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Plasma Levels of microRNA-145 Are Associated with Severity of Coronary Artery Disease

BACKGROUND AND OBJECTIVE: MicroRNAs (miRNAs) have been shown to be associated with various physiological and pathological conditions, including inflammation and cardiovascular disease, but little is known about their relationship with the presence of coronary artery disease (CAD) and disease severit...

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Autores principales: Gao, Hai, Guddeti, Raviteja Reddy, Matsuzawa, Yasushi, Liu, Li-Ping, Su, Li-Xiao, Guo, Duo, Nie, Shao-Ping, Du, Jie, Zhang, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4418743/
https://www.ncbi.nlm.nih.gov/pubmed/25938589
http://dx.doi.org/10.1371/journal.pone.0123477
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author Gao, Hai
Guddeti, Raviteja Reddy
Matsuzawa, Yasushi
Liu, Li-Ping
Su, Li-Xiao
Guo, Duo
Nie, Shao-Ping
Du, Jie
Zhang, Ming
author_facet Gao, Hai
Guddeti, Raviteja Reddy
Matsuzawa, Yasushi
Liu, Li-Ping
Su, Li-Xiao
Guo, Duo
Nie, Shao-Ping
Du, Jie
Zhang, Ming
author_sort Gao, Hai
collection PubMed
description BACKGROUND AND OBJECTIVE: MicroRNAs (miRNAs) have been shown to be associated with various physiological and pathological conditions, including inflammation and cardiovascular disease, but little is known about their relationship with the presence of coronary artery disease (CAD) and disease severity. METHODS: A total of 195 consecutive subjects who underwent coronary angiography for chest pain evaluation were enrolled in this study. In CAD patients severity of coronary lesions was assessed by the number of diseased vessels and the Synergy between PCI with Taxus and Cardiac surgery score (SYNTAX score). Plasma levels of miRNA-145 were quantified by real-time quantitative polymerase chain reaction test, and logarithmic transformation of miRNA-145 levels (Ln_miRNA-145) was used for analyses due to its skewed distribution. RESULTS: Of the 195 total subjects 167 patients were diagnosed as having CAD. Ln_miRNA-145 was significantly lower in CAD patients compared with the non-CAD group (-6.11±0.92 vs. -5.06±1.25; p <0.001). In multivariable linear regression analyses CAD was significantly associated with lower Ln_miRNA-145 (Estimate, -0.50; standard error (SE), 0.11; p <0.0001). Furthermore, among CAD patients, three-vessel disease, higher SYNTAX scores and STEMI were significantly associated with lower Ln_miRNA-145 ([Estimate, -0.40; SE, 0.07; p <0.0001]; [Estimate, -0.02, SE, 0.10; p = 0.005] and [Estimate, -0.35, SE, 0.10; p <0.001] respectively). CONCLUSIONS: Lower plasma levels of miRNA-145 were significantly associated with the presence as well as severity of CAD. As a potential biomarker for CAD, plasma miRNA-145 may be useful in predicting CAD and its severity in patients presenting with chest pain.
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spelling pubmed-44187432015-05-12 Plasma Levels of microRNA-145 Are Associated with Severity of Coronary Artery Disease Gao, Hai Guddeti, Raviteja Reddy Matsuzawa, Yasushi Liu, Li-Ping Su, Li-Xiao Guo, Duo Nie, Shao-Ping Du, Jie Zhang, Ming PLoS One Research Article BACKGROUND AND OBJECTIVE: MicroRNAs (miRNAs) have been shown to be associated with various physiological and pathological conditions, including inflammation and cardiovascular disease, but little is known about their relationship with the presence of coronary artery disease (CAD) and disease severity. METHODS: A total of 195 consecutive subjects who underwent coronary angiography for chest pain evaluation were enrolled in this study. In CAD patients severity of coronary lesions was assessed by the number of diseased vessels and the Synergy between PCI with Taxus and Cardiac surgery score (SYNTAX score). Plasma levels of miRNA-145 were quantified by real-time quantitative polymerase chain reaction test, and logarithmic transformation of miRNA-145 levels (Ln_miRNA-145) was used for analyses due to its skewed distribution. RESULTS: Of the 195 total subjects 167 patients were diagnosed as having CAD. Ln_miRNA-145 was significantly lower in CAD patients compared with the non-CAD group (-6.11±0.92 vs. -5.06±1.25; p <0.001). In multivariable linear regression analyses CAD was significantly associated with lower Ln_miRNA-145 (Estimate, -0.50; standard error (SE), 0.11; p <0.0001). Furthermore, among CAD patients, three-vessel disease, higher SYNTAX scores and STEMI were significantly associated with lower Ln_miRNA-145 ([Estimate, -0.40; SE, 0.07; p <0.0001]; [Estimate, -0.02, SE, 0.10; p = 0.005] and [Estimate, -0.35, SE, 0.10; p <0.001] respectively). CONCLUSIONS: Lower plasma levels of miRNA-145 were significantly associated with the presence as well as severity of CAD. As a potential biomarker for CAD, plasma miRNA-145 may be useful in predicting CAD and its severity in patients presenting with chest pain. Public Library of Science 2015-05-04 /pmc/articles/PMC4418743/ /pubmed/25938589 http://dx.doi.org/10.1371/journal.pone.0123477 Text en © 2015 Gao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gao, Hai
Guddeti, Raviteja Reddy
Matsuzawa, Yasushi
Liu, Li-Ping
Su, Li-Xiao
Guo, Duo
Nie, Shao-Ping
Du, Jie
Zhang, Ming
Plasma Levels of microRNA-145 Are Associated with Severity of Coronary Artery Disease
title Plasma Levels of microRNA-145 Are Associated with Severity of Coronary Artery Disease
title_full Plasma Levels of microRNA-145 Are Associated with Severity of Coronary Artery Disease
title_fullStr Plasma Levels of microRNA-145 Are Associated with Severity of Coronary Artery Disease
title_full_unstemmed Plasma Levels of microRNA-145 Are Associated with Severity of Coronary Artery Disease
title_short Plasma Levels of microRNA-145 Are Associated with Severity of Coronary Artery Disease
title_sort plasma levels of microrna-145 are associated with severity of coronary artery disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4418743/
https://www.ncbi.nlm.nih.gov/pubmed/25938589
http://dx.doi.org/10.1371/journal.pone.0123477
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