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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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.
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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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