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Circulating microparticle concentrations across acute and chronic cardiovascular disease conditions

Concentrations of different circulating microparticles (MPs) may have clinical and physiological relevance to cardiovascular disease pathologies. PURPOSE: To quantify plasma concentrations of CD31+/CD42b−, CD62E+, and CD34+ MPs across healthy individuals and those with coronary artery disease (CAD)...

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Autores principales: Landers‐Ramos, Rian Q., Addison, Odessa A., Beamer, Brock, Katzel, Leslie I., Blumenthal, Jacob B., Robinson, Shawn, Hagberg, James M., Prior, Steven J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399362/
https://www.ncbi.nlm.nih.gov/pubmed/32748505
http://dx.doi.org/10.14814/phy2.14534
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author Landers‐Ramos, Rian Q.
Addison, Odessa A.
Beamer, Brock
Katzel, Leslie I.
Blumenthal, Jacob B.
Robinson, Shawn
Hagberg, James M.
Prior, Steven J.
author_facet Landers‐Ramos, Rian Q.
Addison, Odessa A.
Beamer, Brock
Katzel, Leslie I.
Blumenthal, Jacob B.
Robinson, Shawn
Hagberg, James M.
Prior, Steven J.
author_sort Landers‐Ramos, Rian Q.
collection PubMed
description Concentrations of different circulating microparticles (MPs) may have clinical and physiological relevance to cardiovascular disease pathologies. PURPOSE: To quantify plasma concentrations of CD31+/CD42b−, CD62E+, and CD34+ MPs across healthy individuals and those with coronary artery disease (CAD) or acute cardiovascular events (non‐ST elevation myocardial infarction (NSTEMI)). Fasted blood was obtained from CAD patients (n = 10), NSTEMI patients (n = 13), and healthy older men (n = 15) 60–75 years old. METHODS: CD31+/CD42b−, CD62E+, and CD34+ MPs were isolated from plasma and quantified using flow cytometry. Relationships between MP subtypes, fasting blood lipids, blood glucose, blood pressure, body mass index, and total number of medications were assessed. RESULTS: Concentrations of CD31+/CD42b− MPs were significantly lower in CAD and NSTEMI subjects compared with healthy individuals (p = .02 and .003, respectively). No differences between groups were found for CD62E+ or CD34+ MPs (p > .05 for both). Surprisingly, among all variables assessed, only CD62E+ MP concentrations were positively correlated with triglyceride levels (p = .012) and inversely correlated with SBP (p = .03). CONCLUSIONS: Our findings provide support for the use of different MP subtypes, specifically CD31+/CD42b− MPs, as a potential biomarker of cardiovascular disease. Importantly, results from this study should be looked at in adjunct to previous MP work in CVD conditions as a way of highlighting the complex interactions of variables such as comorbid conditions and medications on MP concentrations.
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spelling pubmed-73993622020-08-06 Circulating microparticle concentrations across acute and chronic cardiovascular disease conditions Landers‐Ramos, Rian Q. Addison, Odessa A. Beamer, Brock Katzel, Leslie I. Blumenthal, Jacob B. Robinson, Shawn Hagberg, James M. Prior, Steven J. Physiol Rep Original Research Concentrations of different circulating microparticles (MPs) may have clinical and physiological relevance to cardiovascular disease pathologies. PURPOSE: To quantify plasma concentrations of CD31+/CD42b−, CD62E+, and CD34+ MPs across healthy individuals and those with coronary artery disease (CAD) or acute cardiovascular events (non‐ST elevation myocardial infarction (NSTEMI)). Fasted blood was obtained from CAD patients (n = 10), NSTEMI patients (n = 13), and healthy older men (n = 15) 60–75 years old. METHODS: CD31+/CD42b−, CD62E+, and CD34+ MPs were isolated from plasma and quantified using flow cytometry. Relationships between MP subtypes, fasting blood lipids, blood glucose, blood pressure, body mass index, and total number of medications were assessed. RESULTS: Concentrations of CD31+/CD42b− MPs were significantly lower in CAD and NSTEMI subjects compared with healthy individuals (p = .02 and .003, respectively). No differences between groups were found for CD62E+ or CD34+ MPs (p > .05 for both). Surprisingly, among all variables assessed, only CD62E+ MP concentrations were positively correlated with triglyceride levels (p = .012) and inversely correlated with SBP (p = .03). CONCLUSIONS: Our findings provide support for the use of different MP subtypes, specifically CD31+/CD42b− MPs, as a potential biomarker of cardiovascular disease. Importantly, results from this study should be looked at in adjunct to previous MP work in CVD conditions as a way of highlighting the complex interactions of variables such as comorbid conditions and medications on MP concentrations. John Wiley and Sons Inc. 2020-08-03 /pmc/articles/PMC7399362/ /pubmed/32748505 http://dx.doi.org/10.14814/phy2.14534 Text en © 2020 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Landers‐Ramos, Rian Q.
Addison, Odessa A.
Beamer, Brock
Katzel, Leslie I.
Blumenthal, Jacob B.
Robinson, Shawn
Hagberg, James M.
Prior, Steven J.
Circulating microparticle concentrations across acute and chronic cardiovascular disease conditions
title Circulating microparticle concentrations across acute and chronic cardiovascular disease conditions
title_full Circulating microparticle concentrations across acute and chronic cardiovascular disease conditions
title_fullStr Circulating microparticle concentrations across acute and chronic cardiovascular disease conditions
title_full_unstemmed Circulating microparticle concentrations across acute and chronic cardiovascular disease conditions
title_short Circulating microparticle concentrations across acute and chronic cardiovascular disease conditions
title_sort circulating microparticle concentrations across acute and chronic cardiovascular disease conditions
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399362/
https://www.ncbi.nlm.nih.gov/pubmed/32748505
http://dx.doi.org/10.14814/phy2.14534
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