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A Whole Blood Molecular Signature for Acute Myocardial Infarction
Chest pain is a leading reason patients seek medical evaluation. While assays to detect myocyte death are used to diagnose a heart attack (acute myocardial infarction, AMI), there is no biomarker to indicate an impending cardiac event. Transcriptional patterns present in circulating endothelial cell...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612952/ https://www.ncbi.nlm.nih.gov/pubmed/28947747 http://dx.doi.org/10.1038/s41598-017-12166-0 |
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author | Muse, Evan D. Kramer, Eric R. Wang, Haiying Barrett, Paddy Parviz, Fereshteh Novotny, Mark A. Lasken, Roger S. Jatkoe, Timothy A. Oliveira, Glenn Peng, Hongfan Lu, Jerry Connelly, Mark C. Schilling, Kurt Rao, Chandra Torkamani, Ali Topol, Eric J. |
author_facet | Muse, Evan D. Kramer, Eric R. Wang, Haiying Barrett, Paddy Parviz, Fereshteh Novotny, Mark A. Lasken, Roger S. Jatkoe, Timothy A. Oliveira, Glenn Peng, Hongfan Lu, Jerry Connelly, Mark C. Schilling, Kurt Rao, Chandra Torkamani, Ali Topol, Eric J. |
author_sort | Muse, Evan D. |
collection | PubMed |
description | Chest pain is a leading reason patients seek medical evaluation. While assays to detect myocyte death are used to diagnose a heart attack (acute myocardial infarction, AMI), there is no biomarker to indicate an impending cardiac event. Transcriptional patterns present in circulating endothelial cells (CEC) may provide a window into the plaque rupture process and identify a proximal biomarker for AMI. Thus, we aimed to identify a transcriptomic signature of AMI present in whole blood, but derived from CECs. Candidate genes indicative of AMI were nominated from microarray of enriched CEC samples, and then verified for detectability and predictive potential via qPCR in whole blood. This signature was validated in an independent cohort. Our findings suggest that a whole blood CEC-derived molecular signature identifies patients with AMI and sets the framework to potentially identify the earlier stages of an impending cardiac event when used in concert with clinical history and other diagnostics where conventional biomarkers indicative of myonecrosis remain undetected. |
format | Online Article Text |
id | pubmed-5612952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56129522017-10-11 A Whole Blood Molecular Signature for Acute Myocardial Infarction Muse, Evan D. Kramer, Eric R. Wang, Haiying Barrett, Paddy Parviz, Fereshteh Novotny, Mark A. Lasken, Roger S. Jatkoe, Timothy A. Oliveira, Glenn Peng, Hongfan Lu, Jerry Connelly, Mark C. Schilling, Kurt Rao, Chandra Torkamani, Ali Topol, Eric J. Sci Rep Article Chest pain is a leading reason patients seek medical evaluation. While assays to detect myocyte death are used to diagnose a heart attack (acute myocardial infarction, AMI), there is no biomarker to indicate an impending cardiac event. Transcriptional patterns present in circulating endothelial cells (CEC) may provide a window into the plaque rupture process and identify a proximal biomarker for AMI. Thus, we aimed to identify a transcriptomic signature of AMI present in whole blood, but derived from CECs. Candidate genes indicative of AMI were nominated from microarray of enriched CEC samples, and then verified for detectability and predictive potential via qPCR in whole blood. This signature was validated in an independent cohort. Our findings suggest that a whole blood CEC-derived molecular signature identifies patients with AMI and sets the framework to potentially identify the earlier stages of an impending cardiac event when used in concert with clinical history and other diagnostics where conventional biomarkers indicative of myonecrosis remain undetected. Nature Publishing Group UK 2017-09-25 /pmc/articles/PMC5612952/ /pubmed/28947747 http://dx.doi.org/10.1038/s41598-017-12166-0 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 Muse, Evan D. Kramer, Eric R. Wang, Haiying Barrett, Paddy Parviz, Fereshteh Novotny, Mark A. Lasken, Roger S. Jatkoe, Timothy A. Oliveira, Glenn Peng, Hongfan Lu, Jerry Connelly, Mark C. Schilling, Kurt Rao, Chandra Torkamani, Ali Topol, Eric J. A Whole Blood Molecular Signature for Acute Myocardial Infarction |
title | A Whole Blood Molecular Signature for Acute Myocardial Infarction |
title_full | A Whole Blood Molecular Signature for Acute Myocardial Infarction |
title_fullStr | A Whole Blood Molecular Signature for Acute Myocardial Infarction |
title_full_unstemmed | A Whole Blood Molecular Signature for Acute Myocardial Infarction |
title_short | A Whole Blood Molecular Signature for Acute Myocardial Infarction |
title_sort | whole blood molecular signature for acute myocardial infarction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612952/ https://www.ncbi.nlm.nih.gov/pubmed/28947747 http://dx.doi.org/10.1038/s41598-017-12166-0 |
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