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Circulating microRNAs: a novel potential biomarker for diagnosing acute aortic dissection

Acute aortic dissection (AAD) is a catastrophic emergency with high mortality and misdiagnosis rate. We aimed to determine whether circulating microRNAs allow to distinguish AAD from healthy controls and chest pain patients without AAD (CP). Plasma microRNAs expression were determined in 103 partici...

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Autores principales: Dong, Jian, Bao, Junmin, Feng, Rui, Zhao, Zhiqing, Lu, Qingsheng, Wang, Guokun, Li, Haiyan, Su, Dingfeng, Zhou, Jian, Jing, Qing, Jing, Zaiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630636/
https://www.ncbi.nlm.nih.gov/pubmed/28986538
http://dx.doi.org/10.1038/s41598-017-13104-w
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author Dong, Jian
Bao, Junmin
Feng, Rui
Zhao, Zhiqing
Lu, Qingsheng
Wang, Guokun
Li, Haiyan
Su, Dingfeng
Zhou, Jian
Jing, Qing
Jing, Zaiping
author_facet Dong, Jian
Bao, Junmin
Feng, Rui
Zhao, Zhiqing
Lu, Qingsheng
Wang, Guokun
Li, Haiyan
Su, Dingfeng
Zhou, Jian
Jing, Qing
Jing, Zaiping
author_sort Dong, Jian
collection PubMed
description Acute aortic dissection (AAD) is a catastrophic emergency with high mortality and misdiagnosis rate. We aimed to determine whether circulating microRNAs allow to distinguish AAD from healthy controls and chest pain patients without AAD (CP). Plasma microRNAs expression were determined in 103 participants, including 37 AAD patients, 26 chronic aortic dissection patients, 17 healthy volunteers, 23 patients without AAD. We selected 16 microRNAs from microarray screening as candidates for further testing via qRT-PCR. The results showed that plasma miR-15a in patients with AAD (n = 37) had significantly higher expression levels than it from control group (n = 40; P = 0.008). By receiver operating characteristic curve analysis, the sensitivity was 75.7%; the specificity was 82.5%; and the AUC was 0.761 for detection of AAD. Furthermore, 37 patients with AAD had significantly higher plasma expression levels of let-7b, miR-15a, miR-23a and hcmv-miR-US33-5p compared with 14 CP patients of 40 controls (P = 0.000, 0.000, 0.026 and 0.011, respectively). The corresponding sensitivity were 79.4%, 75.7%, 91.9% and 73.5%, respectively; the specificity were 92.9%, 100%, 85.7% and 85.7%, respectively; and the AUCs of these microRNAs were 0.887, 0.855, 0.925 and 0.815, respectively. These data indicate that plasma miR-15a and miR-23a have promising clinical value in diagnosing AAD.
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spelling pubmed-56306362017-10-17 Circulating microRNAs: a novel potential biomarker for diagnosing acute aortic dissection Dong, Jian Bao, Junmin Feng, Rui Zhao, Zhiqing Lu, Qingsheng Wang, Guokun Li, Haiyan Su, Dingfeng Zhou, Jian Jing, Qing Jing, Zaiping Sci Rep Article Acute aortic dissection (AAD) is a catastrophic emergency with high mortality and misdiagnosis rate. We aimed to determine whether circulating microRNAs allow to distinguish AAD from healthy controls and chest pain patients without AAD (CP). Plasma microRNAs expression were determined in 103 participants, including 37 AAD patients, 26 chronic aortic dissection patients, 17 healthy volunteers, 23 patients without AAD. We selected 16 microRNAs from microarray screening as candidates for further testing via qRT-PCR. The results showed that plasma miR-15a in patients with AAD (n = 37) had significantly higher expression levels than it from control group (n = 40; P = 0.008). By receiver operating characteristic curve analysis, the sensitivity was 75.7%; the specificity was 82.5%; and the AUC was 0.761 for detection of AAD. Furthermore, 37 patients with AAD had significantly higher plasma expression levels of let-7b, miR-15a, miR-23a and hcmv-miR-US33-5p compared with 14 CP patients of 40 controls (P = 0.000, 0.000, 0.026 and 0.011, respectively). The corresponding sensitivity were 79.4%, 75.7%, 91.9% and 73.5%, respectively; the specificity were 92.9%, 100%, 85.7% and 85.7%, respectively; and the AUCs of these microRNAs were 0.887, 0.855, 0.925 and 0.815, respectively. These data indicate that plasma miR-15a and miR-23a have promising clinical value in diagnosing AAD. Nature Publishing Group UK 2017-10-06 /pmc/articles/PMC5630636/ /pubmed/28986538 http://dx.doi.org/10.1038/s41598-017-13104-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Dong, Jian
Bao, Junmin
Feng, Rui
Zhao, Zhiqing
Lu, Qingsheng
Wang, Guokun
Li, Haiyan
Su, Dingfeng
Zhou, Jian
Jing, Qing
Jing, Zaiping
Circulating microRNAs: a novel potential biomarker for diagnosing acute aortic dissection
title Circulating microRNAs: a novel potential biomarker for diagnosing acute aortic dissection
title_full Circulating microRNAs: a novel potential biomarker for diagnosing acute aortic dissection
title_fullStr Circulating microRNAs: a novel potential biomarker for diagnosing acute aortic dissection
title_full_unstemmed Circulating microRNAs: a novel potential biomarker for diagnosing acute aortic dissection
title_short Circulating microRNAs: a novel potential biomarker for diagnosing acute aortic dissection
title_sort circulating micrornas: a novel potential biomarker for diagnosing acute aortic dissection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630636/
https://www.ncbi.nlm.nih.gov/pubmed/28986538
http://dx.doi.org/10.1038/s41598-017-13104-w
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