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Clinical impact of circulating miR-133, miR-1291 and miR-663b in plasma of patients with acute myocardial infarction

BACKGROUND: Acute myocardial infarction (AMI) is one of the leading causes for death in both developed and developing countries and it is the single largest cause of death in the United States, responsible for 1 out of every 6 deaths. The objective of this study was to determine microRNA (miRNA) exp...

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Autores principales: Peng, Liu, Chun-guang, Qiu, Bei-fang, Li, Xue-zhi, Ding, Zi-hao, Wang, Yun-fu, Li, Yan-ping, Dang, Yang-gui, Liu, Wei-guo, Li, Tian-yong, Hu, Zhen-wen, Huang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4082297/
https://www.ncbi.nlm.nih.gov/pubmed/24885383
http://dx.doi.org/10.1186/1746-1596-9-89
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author Peng, Liu
Chun-guang, Qiu
Bei-fang, Li
Xue-zhi, Ding
Zi-hao, Wang
Yun-fu, Li
Yan-ping, Dang
Yang-gui, Liu
Wei-guo, Li
Tian-yong, Hu
Zhen-wen, Huang
author_facet Peng, Liu
Chun-guang, Qiu
Bei-fang, Li
Xue-zhi, Ding
Zi-hao, Wang
Yun-fu, Li
Yan-ping, Dang
Yang-gui, Liu
Wei-guo, Li
Tian-yong, Hu
Zhen-wen, Huang
author_sort Peng, Liu
collection PubMed
description BACKGROUND: Acute myocardial infarction (AMI) is one of the leading causes for death in both developed and developing countries and it is the single largest cause of death in the United States, responsible for 1 out of every 6 deaths. The objective of this study was to determine microRNA (miRNA) expression in AMI and determine whether miR-133, miR-1291 and miR-663b could be measured in plasma as a biomarker for recurrence. METHODS: Patients with AMI and those without AMI were retrospectively recruited for a comparison of their plasma miR-133, miR-1291 and miR-663b expression. RESULTS: miR-133, miR-1291 and miR-663b levels were significantly overexpressed in AMI compared with Non-AMI. MiR-133 showed an AUC of 0.912, with a sensitivity of 81.1% and a specificity of 91.2%. The AUC for miR-1291 was 0.695, with a sensitivity of 78.4% and a specificity of 89.5%. The AUC for miR-663b was 0.611, with a sensitivity of 72.4% and a specificity of 76.5%. CONCLUSIONS: This study demonstrated that the levels of miR-133, miR-1291 and miR-663b are associated with AMI. The potential of these miRNAs as biomarkers to improve patient stratification according to the risk of AMI and as circulating biomarkers for the AMI progonos warrants further study. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/8183629061241474
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spelling pubmed-40822972014-07-05 Clinical impact of circulating miR-133, miR-1291 and miR-663b in plasma of patients with acute myocardial infarction Peng, Liu Chun-guang, Qiu Bei-fang, Li Xue-zhi, Ding Zi-hao, Wang Yun-fu, Li Yan-ping, Dang Yang-gui, Liu Wei-guo, Li Tian-yong, Hu Zhen-wen, Huang Diagn Pathol Research BACKGROUND: Acute myocardial infarction (AMI) is one of the leading causes for death in both developed and developing countries and it is the single largest cause of death in the United States, responsible for 1 out of every 6 deaths. The objective of this study was to determine microRNA (miRNA) expression in AMI and determine whether miR-133, miR-1291 and miR-663b could be measured in plasma as a biomarker for recurrence. METHODS: Patients with AMI and those without AMI were retrospectively recruited for a comparison of their plasma miR-133, miR-1291 and miR-663b expression. RESULTS: miR-133, miR-1291 and miR-663b levels were significantly overexpressed in AMI compared with Non-AMI. MiR-133 showed an AUC of 0.912, with a sensitivity of 81.1% and a specificity of 91.2%. The AUC for miR-1291 was 0.695, with a sensitivity of 78.4% and a specificity of 89.5%. The AUC for miR-663b was 0.611, with a sensitivity of 72.4% and a specificity of 76.5%. CONCLUSIONS: This study demonstrated that the levels of miR-133, miR-1291 and miR-663b are associated with AMI. The potential of these miRNAs as biomarkers to improve patient stratification according to the risk of AMI and as circulating biomarkers for the AMI progonos warrants further study. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/8183629061241474 BioMed Central 2014-05-01 /pmc/articles/PMC4082297/ /pubmed/24885383 http://dx.doi.org/10.1186/1746-1596-9-89 Text en Copyright © 2014 Peng et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Peng, Liu
Chun-guang, Qiu
Bei-fang, Li
Xue-zhi, Ding
Zi-hao, Wang
Yun-fu, Li
Yan-ping, Dang
Yang-gui, Liu
Wei-guo, Li
Tian-yong, Hu
Zhen-wen, Huang
Clinical impact of circulating miR-133, miR-1291 and miR-663b in plasma of patients with acute myocardial infarction
title Clinical impact of circulating miR-133, miR-1291 and miR-663b in plasma of patients with acute myocardial infarction
title_full Clinical impact of circulating miR-133, miR-1291 and miR-663b in plasma of patients with acute myocardial infarction
title_fullStr Clinical impact of circulating miR-133, miR-1291 and miR-663b in plasma of patients with acute myocardial infarction
title_full_unstemmed Clinical impact of circulating miR-133, miR-1291 and miR-663b in plasma of patients with acute myocardial infarction
title_short Clinical impact of circulating miR-133, miR-1291 and miR-663b in plasma of patients with acute myocardial infarction
title_sort clinical impact of circulating mir-133, mir-1291 and mir-663b in plasma of patients with acute myocardial infarction
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4082297/
https://www.ncbi.nlm.nih.gov/pubmed/24885383
http://dx.doi.org/10.1186/1746-1596-9-89
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