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MicroRNA 21 and microRNA 155 levels in resistant hypertension, and their relationships with aldosterone
AIM: MicroRNAs (miRNAs) are non-coding RNA molecules that serve as regulators following gene expression transcription. While studies have investigated the role of miRNAs in the pathogenesis of essential hypertension (HT), very few have considered their place in the pathogenesis of resistant hyperten...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8078961/ https://www.ncbi.nlm.nih.gov/pubmed/33888045 http://dx.doi.org/10.1080/0886022X.2021.1915800 |
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author | Kara, Sonat Pınar Ozkan, Gulsum Yılmaz, Ahsen Bayrakçı, Nergiz Güzel, Savaş Geyik, Elif |
author_facet | Kara, Sonat Pınar Ozkan, Gulsum Yılmaz, Ahsen Bayrakçı, Nergiz Güzel, Savaş Geyik, Elif |
author_sort | Kara, Sonat Pınar |
collection | PubMed |
description | AIM: MicroRNAs (miRNAs) are non-coding RNA molecules that serve as regulators following gene expression transcription. While studies have investigated the role of miRNAs in the pathogenesis of essential hypertension (HT), very few have considered their place in the pathogenesis of resistant hypertension (RH). The purpose of this study was to investigate levels of miRNA 21 and miRNA 155 in RH and their relationships with aldosterone. METHOD: Thirty-two normotensive patients, 30 newly diagnosed HT patients, and 20 RH patients were included in the study. Patients’ demographic data were recorded, and office blood pressure measurement and 24-h ambulatory blood pressure monitoring (24-h ABPM) were performed. Blood specimens were collected for miRNA 21, miRNA 155 and aldosterone measurement. MiRNA 21 and miRNA 155 levels in the control and patient groups and their relations with other demographic and biochemical parameters were then subjected to analysis. RESULTS: No difference was determined in miRNA 155 levels between the groups, but miRNA 21 and aldosterone levels were significantly higher in the RH group (p < 0.001 and <0.05, respectively). At correlation analysis, miRNA 21 exhibited positive correlation with aldosterone, age, office SBP, 24-h ABPM all-day SBP. A 9.6 copy/uL level for miRNA 21 predicted presence or absence of RH with 95% sensitivity and 71% specificity (AUC:0.823, 95% CI (0.72–0.92). CONCLUSION: The study results revealed significantly higher miRNA 21 and aldosterone in RH patients than in healthy individuals and newly diagnosed hypertensives. |
format | Online Article Text |
id | pubmed-8078961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-80789612021-05-06 MicroRNA 21 and microRNA 155 levels in resistant hypertension, and their relationships with aldosterone Kara, Sonat Pınar Ozkan, Gulsum Yılmaz, Ahsen Bayrakçı, Nergiz Güzel, Savaş Geyik, Elif Ren Fail Clinical Study AIM: MicroRNAs (miRNAs) are non-coding RNA molecules that serve as regulators following gene expression transcription. While studies have investigated the role of miRNAs in the pathogenesis of essential hypertension (HT), very few have considered their place in the pathogenesis of resistant hypertension (RH). The purpose of this study was to investigate levels of miRNA 21 and miRNA 155 in RH and their relationships with aldosterone. METHOD: Thirty-two normotensive patients, 30 newly diagnosed HT patients, and 20 RH patients were included in the study. Patients’ demographic data were recorded, and office blood pressure measurement and 24-h ambulatory blood pressure monitoring (24-h ABPM) were performed. Blood specimens were collected for miRNA 21, miRNA 155 and aldosterone measurement. MiRNA 21 and miRNA 155 levels in the control and patient groups and their relations with other demographic and biochemical parameters were then subjected to analysis. RESULTS: No difference was determined in miRNA 155 levels between the groups, but miRNA 21 and aldosterone levels were significantly higher in the RH group (p < 0.001 and <0.05, respectively). At correlation analysis, miRNA 21 exhibited positive correlation with aldosterone, age, office SBP, 24-h ABPM all-day SBP. A 9.6 copy/uL level for miRNA 21 predicted presence or absence of RH with 95% sensitivity and 71% specificity (AUC:0.823, 95% CI (0.72–0.92). CONCLUSION: The study results revealed significantly higher miRNA 21 and aldosterone in RH patients than in healthy individuals and newly diagnosed hypertensives. Taylor & Francis 2021-04-23 /pmc/articles/PMC8078961/ /pubmed/33888045 http://dx.doi.org/10.1080/0886022X.2021.1915800 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Kara, Sonat Pınar Ozkan, Gulsum Yılmaz, Ahsen Bayrakçı, Nergiz Güzel, Savaş Geyik, Elif MicroRNA 21 and microRNA 155 levels in resistant hypertension, and their relationships with aldosterone |
title | MicroRNA 21 and microRNA 155 levels in resistant hypertension, and their relationships with aldosterone |
title_full | MicroRNA 21 and microRNA 155 levels in resistant hypertension, and their relationships with aldosterone |
title_fullStr | MicroRNA 21 and microRNA 155 levels in resistant hypertension, and their relationships with aldosterone |
title_full_unstemmed | MicroRNA 21 and microRNA 155 levels in resistant hypertension, and their relationships with aldosterone |
title_short | MicroRNA 21 and microRNA 155 levels in resistant hypertension, and their relationships with aldosterone |
title_sort | microrna 21 and microrna 155 levels in resistant hypertension, and their relationships with aldosterone |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8078961/ https://www.ncbi.nlm.nih.gov/pubmed/33888045 http://dx.doi.org/10.1080/0886022X.2021.1915800 |
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