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Circulating microRNAs and vascular calcification in hemodialysis patients

OBJECTIVE: Vascular calcification is common in chronic dialysis patients and is associated with increased morbidity and mortality. However, the role of circulating microRNAs (miRs) in vascular calcification has rarely been investigated. We aimed to determine circulating levels of miRs in hemodialysi...

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Autores principales: Lee, Chien-Te, Lee, Yueh-Ting, Tain, You-Lin, Ng, Hwee-Yeong, Kuo, Wei-Hung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6683928/
https://www.ncbi.nlm.nih.gov/pubmed/31144545
http://dx.doi.org/10.1177/0300060519848949
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author Lee, Chien-Te
Lee, Yueh-Ting
Tain, You-Lin
Ng, Hwee-Yeong
Kuo, Wei-Hung
author_facet Lee, Chien-Te
Lee, Yueh-Ting
Tain, You-Lin
Ng, Hwee-Yeong
Kuo, Wei-Hung
author_sort Lee, Chien-Te
collection PubMed
description OBJECTIVE: Vascular calcification is common in chronic dialysis patients and is associated with increased morbidity and mortality. However, the role of circulating microRNAs (miRs) in vascular calcification has rarely been investigated. We aimed to determine circulating levels of miRs in hemodialysis patients, and analyzed their relationship with vascular calcification. METHODS: Sixty-one stable hemodialysis patients were enrolled, including 31 with vascular calcification and 30 without. Demographic and biochemical data were collected and reviewed. The presence and severity of vascular calcification were determined by lumber spine X-ray. Blood levels of miR29a/b, miR223, miR9, and miR21 were determined. RESULTS: Patients with vascular calcification were older (65.6 ± 9.0 vs. 59.1 ± 7.1 years) with a higher proportion of vascular disease (55% vs. 23%) than those without vascular calcification. Additionally, high-sensitivity C-reactive protein (3.90 vs 2.09 mg/dL) and fibroblast growth factor 23 (17311 vs. 6306 pg/mL) were significantly higher. Patients with vascular calcification also had higher levels of miR29a/b and miR223. Regression analysis indicated that age and miR29a were significant associates of the calcification score. CONCLUSIONS: Hemodialysis patients with vascular calcification had higher levels of miR 29a/b and miR223 than those without vascular calcification, and circulating miR29a was associated with calcification severity.
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spelling pubmed-66839282019-08-19 Circulating microRNAs and vascular calcification in hemodialysis patients Lee, Chien-Te Lee, Yueh-Ting Tain, You-Lin Ng, Hwee-Yeong Kuo, Wei-Hung J Int Med Res Clinical Research Reports OBJECTIVE: Vascular calcification is common in chronic dialysis patients and is associated with increased morbidity and mortality. However, the role of circulating microRNAs (miRs) in vascular calcification has rarely been investigated. We aimed to determine circulating levels of miRs in hemodialysis patients, and analyzed their relationship with vascular calcification. METHODS: Sixty-one stable hemodialysis patients were enrolled, including 31 with vascular calcification and 30 without. Demographic and biochemical data were collected and reviewed. The presence and severity of vascular calcification were determined by lumber spine X-ray. Blood levels of miR29a/b, miR223, miR9, and miR21 were determined. RESULTS: Patients with vascular calcification were older (65.6 ± 9.0 vs. 59.1 ± 7.1 years) with a higher proportion of vascular disease (55% vs. 23%) than those without vascular calcification. Additionally, high-sensitivity C-reactive protein (3.90 vs 2.09 mg/dL) and fibroblast growth factor 23 (17311 vs. 6306 pg/mL) were significantly higher. Patients with vascular calcification also had higher levels of miR29a/b and miR223. Regression analysis indicated that age and miR29a were significant associates of the calcification score. CONCLUSIONS: Hemodialysis patients with vascular calcification had higher levels of miR 29a/b and miR223 than those without vascular calcification, and circulating miR29a was associated with calcification severity. SAGE Publications 2019-05-30 2019-07 /pmc/articles/PMC6683928/ /pubmed/31144545 http://dx.doi.org/10.1177/0300060519848949 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.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 pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Clinical Research Reports
Lee, Chien-Te
Lee, Yueh-Ting
Tain, You-Lin
Ng, Hwee-Yeong
Kuo, Wei-Hung
Circulating microRNAs and vascular calcification in hemodialysis patients
title Circulating microRNAs and vascular calcification in hemodialysis patients
title_full Circulating microRNAs and vascular calcification in hemodialysis patients
title_fullStr Circulating microRNAs and vascular calcification in hemodialysis patients
title_full_unstemmed Circulating microRNAs and vascular calcification in hemodialysis patients
title_short Circulating microRNAs and vascular calcification in hemodialysis patients
title_sort circulating micrornas and vascular calcification in hemodialysis patients
topic Clinical Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6683928/
https://www.ncbi.nlm.nih.gov/pubmed/31144545
http://dx.doi.org/10.1177/0300060519848949
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