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Circulating microRNA-1 in the diagnosis and predicting prognosis of patients with chest pain: a prospective cohort study

BACKGROUND: To investigate the early diagnostic and prognostic value of microRNA-1 in patients with acute chest pain. METHODS: This study enrolled 341 patients attacked by chest pain within 3 h, and another 100 volunteers as control group. Circulating microRNA-1 was collected and determined by real-...

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Autores principales: Su, Tong, Shao, Xiaonan, Zhang, Xiaopu, Han, Zhijun, Yang, Chengjian, Li, Xun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321730/
https://www.ncbi.nlm.nih.gov/pubmed/30611212
http://dx.doi.org/10.1186/s12872-018-0987-x
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author Su, Tong
Shao, Xiaonan
Zhang, Xiaopu
Han, Zhijun
Yang, Chengjian
Li, Xun
author_facet Su, Tong
Shao, Xiaonan
Zhang, Xiaopu
Han, Zhijun
Yang, Chengjian
Li, Xun
author_sort Su, Tong
collection PubMed
description BACKGROUND: To investigate the early diagnostic and prognostic value of microRNA-1 in patients with acute chest pain. METHODS: This study enrolled 341 patients attacked by chest pain within 3 h, and another 100 volunteers as control group. Circulating microRNA-1 was collected and determined by real-time quantitative reverse transcription-polymerase chain reaction. The clinical follow-up period was 720 days. RESULTS: There were 174 patients in acute myocardial infarction (AMI) group, 167 in non-AMI group. The relative expression of microRNA-1 was significantly increased within 3 h in AMI group, and it continued rising within 12 h, lower at 24 h than that 12 h in AMI group without reperfusion therapy. Otherwise, microRNA-1 concentration was markedly low at 12 h after primary percutaneous coronary intervention in AMI group. The 95% reference range of circulating microRNA-1 was 0.171–0.653. It was significantly available for microRNA-1 to early diagnose AMI with an optimal cutoff value of 2.215 and diagnostic accuracy could be improved when combined with cardiac troponin I. It was not statistically significant for microRNA-1 to forecast future AMI but might prognose mortality of 720 days in chest pain patients. In patients with chest pain, microRNA-1 concentration was high with major adverse cardiac events within 30 days, low with high overall survival within 720 days. CONCLUSIONS: Circulating microRNA-1 might diagnose early AMI and predict the prognosis of patients with chest pain.
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spelling pubmed-63217302019-01-09 Circulating microRNA-1 in the diagnosis and predicting prognosis of patients with chest pain: a prospective cohort study Su, Tong Shao, Xiaonan Zhang, Xiaopu Han, Zhijun Yang, Chengjian Li, Xun BMC Cardiovasc Disord Research Article BACKGROUND: To investigate the early diagnostic and prognostic value of microRNA-1 in patients with acute chest pain. METHODS: This study enrolled 341 patients attacked by chest pain within 3 h, and another 100 volunteers as control group. Circulating microRNA-1 was collected and determined by real-time quantitative reverse transcription-polymerase chain reaction. The clinical follow-up period was 720 days. RESULTS: There were 174 patients in acute myocardial infarction (AMI) group, 167 in non-AMI group. The relative expression of microRNA-1 was significantly increased within 3 h in AMI group, and it continued rising within 12 h, lower at 24 h than that 12 h in AMI group without reperfusion therapy. Otherwise, microRNA-1 concentration was markedly low at 12 h after primary percutaneous coronary intervention in AMI group. The 95% reference range of circulating microRNA-1 was 0.171–0.653. It was significantly available for microRNA-1 to early diagnose AMI with an optimal cutoff value of 2.215 and diagnostic accuracy could be improved when combined with cardiac troponin I. It was not statistically significant for microRNA-1 to forecast future AMI but might prognose mortality of 720 days in chest pain patients. In patients with chest pain, microRNA-1 concentration was high with major adverse cardiac events within 30 days, low with high overall survival within 720 days. CONCLUSIONS: Circulating microRNA-1 might diagnose early AMI and predict the prognosis of patients with chest pain. BioMed Central 2019-01-05 /pmc/articles/PMC6321730/ /pubmed/30611212 http://dx.doi.org/10.1186/s12872-018-0987-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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 Article
Su, Tong
Shao, Xiaonan
Zhang, Xiaopu
Han, Zhijun
Yang, Chengjian
Li, Xun
Circulating microRNA-1 in the diagnosis and predicting prognosis of patients with chest pain: a prospective cohort study
title Circulating microRNA-1 in the diagnosis and predicting prognosis of patients with chest pain: a prospective cohort study
title_full Circulating microRNA-1 in the diagnosis and predicting prognosis of patients with chest pain: a prospective cohort study
title_fullStr Circulating microRNA-1 in the diagnosis and predicting prognosis of patients with chest pain: a prospective cohort study
title_full_unstemmed Circulating microRNA-1 in the diagnosis and predicting prognosis of patients with chest pain: a prospective cohort study
title_short Circulating microRNA-1 in the diagnosis and predicting prognosis of patients with chest pain: a prospective cohort study
title_sort circulating microrna-1 in the diagnosis and predicting prognosis of patients with chest pain: a prospective cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321730/
https://www.ncbi.nlm.nih.gov/pubmed/30611212
http://dx.doi.org/10.1186/s12872-018-0987-x
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