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Circulating Extracellular miRNA Analysis in Patients with Stable CAD and Acute Coronary Syndromes
Extracellular circulating microRNAs (miRNAs) are currently a focus of interest as non-invasive biomarkers of cardiovascular pathologies, including coronary artery disease (CAD) and acute coronary syndromes (ACS): myocardial infarction with and without ST-segment elevation (STEMI and NSTEMI) and unst...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301961/ https://www.ncbi.nlm.nih.gov/pubmed/34209965 http://dx.doi.org/10.3390/biom11070962 |
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author | Zhelankin, Andrey V. Stonogina, Daria A. Vasiliev, Sergey V. Babalyan, Konstantin A. Sharova, Elena I. Doludin, Yurii V. Shchekochikhin, Dmitry Y. Generozov, Eduard V. Akselrod, Anna S. |
author_facet | Zhelankin, Andrey V. Stonogina, Daria A. Vasiliev, Sergey V. Babalyan, Konstantin A. Sharova, Elena I. Doludin, Yurii V. Shchekochikhin, Dmitry Y. Generozov, Eduard V. Akselrod, Anna S. |
author_sort | Zhelankin, Andrey V. |
collection | PubMed |
description | Extracellular circulating microRNAs (miRNAs) are currently a focus of interest as non-invasive biomarkers of cardiovascular pathologies, including coronary artery disease (CAD) and acute coronary syndromes (ACS): myocardial infarction with and without ST-segment elevation (STEMI and NSTEMI) and unstable angina (UA). However, the current data for some miRNAs are controversial and inconsistent, probably due to pre-analytical and methodological variances in different studies. In this work, we fulfilled the basic pre-analytical requirements provided for circulating miRNA studies for application to stable CAD and ACS research. We used quantitative PCR to determine the relative plasma levels of eight circulating miRNAs that are potentially associated with atherosclerosis. In a cohort of 136 adult clinic CAD patients and outpatient controls, we found that the plasma levels of miR-21-5p and miR-146a-5p were significantly elevated in ACS patients, and the level of miR-17-5p was decreased in ACS and stable CAD patients compared to both healthy controls and hypertensive patients without CAD. Within the ACS patient group, no differences were found in the plasma levels of these miRNAs between patients with positive and negative troponin, nor were any differences found between STEMI and NSTEMI. Our results indicate that increased plasma levels of miR-146a-5p and miR-21-5p can be considered general ACS circulating biomarkers and that lowered miR-17-5p can be considered a general biomarker of CAD. |
format | Online Article Text |
id | pubmed-8301961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83019612021-07-24 Circulating Extracellular miRNA Analysis in Patients with Stable CAD and Acute Coronary Syndromes Zhelankin, Andrey V. Stonogina, Daria A. Vasiliev, Sergey V. Babalyan, Konstantin A. Sharova, Elena I. Doludin, Yurii V. Shchekochikhin, Dmitry Y. Generozov, Eduard V. Akselrod, Anna S. Biomolecules Article Extracellular circulating microRNAs (miRNAs) are currently a focus of interest as non-invasive biomarkers of cardiovascular pathologies, including coronary artery disease (CAD) and acute coronary syndromes (ACS): myocardial infarction with and without ST-segment elevation (STEMI and NSTEMI) and unstable angina (UA). However, the current data for some miRNAs are controversial and inconsistent, probably due to pre-analytical and methodological variances in different studies. In this work, we fulfilled the basic pre-analytical requirements provided for circulating miRNA studies for application to stable CAD and ACS research. We used quantitative PCR to determine the relative plasma levels of eight circulating miRNAs that are potentially associated with atherosclerosis. In a cohort of 136 adult clinic CAD patients and outpatient controls, we found that the plasma levels of miR-21-5p and miR-146a-5p were significantly elevated in ACS patients, and the level of miR-17-5p was decreased in ACS and stable CAD patients compared to both healthy controls and hypertensive patients without CAD. Within the ACS patient group, no differences were found in the plasma levels of these miRNAs between patients with positive and negative troponin, nor were any differences found between STEMI and NSTEMI. Our results indicate that increased plasma levels of miR-146a-5p and miR-21-5p can be considered general ACS circulating biomarkers and that lowered miR-17-5p can be considered a general biomarker of CAD. MDPI 2021-06-29 /pmc/articles/PMC8301961/ /pubmed/34209965 http://dx.doi.org/10.3390/biom11070962 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhelankin, Andrey V. Stonogina, Daria A. Vasiliev, Sergey V. Babalyan, Konstantin A. Sharova, Elena I. Doludin, Yurii V. Shchekochikhin, Dmitry Y. Generozov, Eduard V. Akselrod, Anna S. Circulating Extracellular miRNA Analysis in Patients with Stable CAD and Acute Coronary Syndromes |
title | Circulating Extracellular miRNA Analysis in Patients with Stable CAD and Acute Coronary Syndromes |
title_full | Circulating Extracellular miRNA Analysis in Patients with Stable CAD and Acute Coronary Syndromes |
title_fullStr | Circulating Extracellular miRNA Analysis in Patients with Stable CAD and Acute Coronary Syndromes |
title_full_unstemmed | Circulating Extracellular miRNA Analysis in Patients with Stable CAD and Acute Coronary Syndromes |
title_short | Circulating Extracellular miRNA Analysis in Patients with Stable CAD and Acute Coronary Syndromes |
title_sort | circulating extracellular mirna analysis in patients with stable cad and acute coronary syndromes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301961/ https://www.ncbi.nlm.nih.gov/pubmed/34209965 http://dx.doi.org/10.3390/biom11070962 |
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