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MicroRNA 486-3P as a stability marker in acute coronary syndrome

Easily accessible biomarkers are needed to diagnose cardiovascular disease precisely—particularly, to distinguish between disease subtypes that are encountered in clinical practice. Per the hypothesis that plasma miRNA is valuable for this purpose, we performed complete transcriptional profiling of...

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Detalles Bibliográficos
Autores principales: Wei, Tianling, Folkersen, Lasse, Ehrenborg, Ewa, Gabrielsen, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293558/
https://www.ncbi.nlm.nih.gov/pubmed/27190129
http://dx.doi.org/10.1042/BSR20160023
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author Wei, Tianling
Folkersen, Lasse
Ehrenborg, Ewa
Gabrielsen, Anders
author_facet Wei, Tianling
Folkersen, Lasse
Ehrenborg, Ewa
Gabrielsen, Anders
author_sort Wei, Tianling
collection PubMed
description Easily accessible biomarkers are needed to diagnose cardiovascular disease precisely—particularly, to distinguish between disease subtypes that are encountered in clinical practice. Per the hypothesis that plasma miRNA is valuable for this purpose, we performed complete transcriptional profiling of an miRNA discovery-set in 14 samples: three patients with ST-elevated acute myocardial infarction (STEMI) at baseline and after three months of follow-up, four with stable ischaemic heart disease (stable-IHD) and four healthy age-matched volunteers. Our aim was to determine whether we could distinguish patients with unstable plaques from stable patients following a STEMI event. After analysing miRNA profiles, we conducted a validation study comparing three-month STEMI (n=40) with stable-IHD (n=35), which confirmed that miR-486-3P differentiates patients with three-month STEMI from those with stable-IHD (P=0.019).
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spelling pubmed-52935582017-02-14 MicroRNA 486-3P as a stability marker in acute coronary syndrome Wei, Tianling Folkersen, Lasse Ehrenborg, Ewa Gabrielsen, Anders Biosci Rep Original Papers Easily accessible biomarkers are needed to diagnose cardiovascular disease precisely—particularly, to distinguish between disease subtypes that are encountered in clinical practice. Per the hypothesis that plasma miRNA is valuable for this purpose, we performed complete transcriptional profiling of an miRNA discovery-set in 14 samples: three patients with ST-elevated acute myocardial infarction (STEMI) at baseline and after three months of follow-up, four with stable ischaemic heart disease (stable-IHD) and four healthy age-matched volunteers. Our aim was to determine whether we could distinguish patients with unstable plaques from stable patients following a STEMI event. After analysing miRNA profiles, we conducted a validation study comparing three-month STEMI (n=40) with stable-IHD (n=35), which confirmed that miR-486-3P differentiates patients with three-month STEMI from those with stable-IHD (P=0.019). Portland Press Ltd. 2016-06-30 /pmc/articles/PMC5293558/ /pubmed/27190129 http://dx.doi.org/10.1042/BSR20160023 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution Licence 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Papers
Wei, Tianling
Folkersen, Lasse
Ehrenborg, Ewa
Gabrielsen, Anders
MicroRNA 486-3P as a stability marker in acute coronary syndrome
title MicroRNA 486-3P as a stability marker in acute coronary syndrome
title_full MicroRNA 486-3P as a stability marker in acute coronary syndrome
title_fullStr MicroRNA 486-3P as a stability marker in acute coronary syndrome
title_full_unstemmed MicroRNA 486-3P as a stability marker in acute coronary syndrome
title_short MicroRNA 486-3P as a stability marker in acute coronary syndrome
title_sort microrna 486-3p as a stability marker in acute coronary syndrome
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293558/
https://www.ncbi.nlm.nih.gov/pubmed/27190129
http://dx.doi.org/10.1042/BSR20160023
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