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Circulating miR-27b as a Biomarker of the Development and Progression of Carotid Artery Stenosis
OBJECTIVE: A close relationship of microRNAs (miRNAs) with various human diseases has been widely reported, including cardiovascular disease. The current study attempted to examine the abnormal expression of miR-27b in asymptomatic carotid artery stenosis (ACAS), its diagnostic value and predictive...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649086/ https://www.ncbi.nlm.nih.gov/pubmed/34806417 http://dx.doi.org/10.1177/10760296211057903 |
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author | Lu, Tingting Li, Xin Long, Chunxi Ji, Wenyuan Jiang, Linjun Tian, Jianquan |
author_facet | Lu, Tingting Li, Xin Long, Chunxi Ji, Wenyuan Jiang, Linjun Tian, Jianquan |
author_sort | Lu, Tingting |
collection | PubMed |
description | OBJECTIVE: A close relationship of microRNAs (miRNAs) with various human diseases has been widely reported, including cardiovascular disease. The current study attempted to examine the abnormal expression of miR-27b in asymptomatic carotid artery stenosis (ACAS), its diagnostic value and predictive value for the development of ACAS were also assessed. METHODS: Clinical serum samples were collected from both ACAS patients and healthy individuals, and levels of miR-27b in the clinical samples were detected using Real-time quantitative PCR. Cerebral ischemia events (CIEs) of patients during the 5-year follow-up were collected. The diagnostic and predictive values of serum miR-27b was assessed via plotting Receiver operating characteristic (ROC) and Kaplan-Meier curves. Multivariate cox regression analysis was performed for clinical independent index analysis. RESULTS: ACAS patients had higher levels of miR-27b than the healthy subjects. There were close association of serum miR-27b levels with total cholesterol (TC) level, absence of hypertension and degree of carotid stenosis. High levels of miR-27b could differentiate ACAS cases from healthy subjects, and predicted the high incidence of CIEs. MiR-27b could be used as an independent predictor of cerebrovascular events via multiple Cox regression analysis (P = .031). CONCLUSION: The high level of miR-27b can predict the occurrence of ACAS, and is closely related to the subsequent occurrence of CIEs. The present results provide evidence for circulating miR-27b as a diagnostic and prognostic marker in patients with ACAS. |
format | Online Article Text |
id | pubmed-8649086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-86490862021-12-08 Circulating miR-27b as a Biomarker of the Development and Progression of Carotid Artery Stenosis Lu, Tingting Li, Xin Long, Chunxi Ji, Wenyuan Jiang, Linjun Tian, Jianquan Clin Appl Thromb Hemost Original Manuscript OBJECTIVE: A close relationship of microRNAs (miRNAs) with various human diseases has been widely reported, including cardiovascular disease. The current study attempted to examine the abnormal expression of miR-27b in asymptomatic carotid artery stenosis (ACAS), its diagnostic value and predictive value for the development of ACAS were also assessed. METHODS: Clinical serum samples were collected from both ACAS patients and healthy individuals, and levels of miR-27b in the clinical samples were detected using Real-time quantitative PCR. Cerebral ischemia events (CIEs) of patients during the 5-year follow-up were collected. The diagnostic and predictive values of serum miR-27b was assessed via plotting Receiver operating characteristic (ROC) and Kaplan-Meier curves. Multivariate cox regression analysis was performed for clinical independent index analysis. RESULTS: ACAS patients had higher levels of miR-27b than the healthy subjects. There were close association of serum miR-27b levels with total cholesterol (TC) level, absence of hypertension and degree of carotid stenosis. High levels of miR-27b could differentiate ACAS cases from healthy subjects, and predicted the high incidence of CIEs. MiR-27b could be used as an independent predictor of cerebrovascular events via multiple Cox regression analysis (P = .031). CONCLUSION: The high level of miR-27b can predict the occurrence of ACAS, and is closely related to the subsequent occurrence of CIEs. The present results provide evidence for circulating miR-27b as a diagnostic and prognostic marker in patients with ACAS. SAGE Publications 2021-11-22 /pmc/articles/PMC8649086/ /pubmed/34806417 http://dx.doi.org/10.1177/10760296211057903 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Manuscript Lu, Tingting Li, Xin Long, Chunxi Ji, Wenyuan Jiang, Linjun Tian, Jianquan Circulating miR-27b as a Biomarker of the Development and Progression of Carotid Artery Stenosis |
title | Circulating miR-27b as a Biomarker of the Development and Progression of Carotid Artery Stenosis |
title_full | Circulating miR-27b as a Biomarker of the Development and Progression of Carotid Artery Stenosis |
title_fullStr | Circulating miR-27b as a Biomarker of the Development and Progression of Carotid Artery Stenosis |
title_full_unstemmed | Circulating miR-27b as a Biomarker of the Development and Progression of Carotid Artery Stenosis |
title_short | Circulating miR-27b as a Biomarker of the Development and Progression of Carotid Artery Stenosis |
title_sort | circulating mir-27b as a biomarker of the development and progression of carotid artery stenosis |
topic | Original Manuscript |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649086/ https://www.ncbi.nlm.nih.gov/pubmed/34806417 http://dx.doi.org/10.1177/10760296211057903 |
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