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Serum osteoprotegerin level is positively associated with peripheral artery disease in patients with peritoneal dialysis
Osteoprotegerin (OPG) is a potential biomarker of cardiovascular disease complications and severity. Peripheral arterial disease (PAD) is associated with an increased risk of death in patients on peritoneal dialysis (PD). Therefore, this study aimed to evaluate the relationship between serum OPG lev...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006676/ https://www.ncbi.nlm.nih.gov/pubmed/31950864 http://dx.doi.org/10.1080/0886022X.2020.1714654 |
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author | Lin, Wei-Chen Tsai, Jen-Pi Lai, Yu-Hsien Lin, Yu-Li Kuo, Chiu-Huang Wang, Chih-Hsien Hsu, Bang-Gee |
author_facet | Lin, Wei-Chen Tsai, Jen-Pi Lai, Yu-Hsien Lin, Yu-Li Kuo, Chiu-Huang Wang, Chih-Hsien Hsu, Bang-Gee |
author_sort | Lin, Wei-Chen |
collection | PubMed |
description | Osteoprotegerin (OPG) is a potential biomarker of cardiovascular disease complications and severity. Peripheral arterial disease (PAD) is associated with an increased risk of death in patients on peritoneal dialysis (PD). Therefore, this study aimed to evaluate the relationship between serum OPG levels and PAD by measuring the ankle-brachial index (ABI) of patients on PD. A commercial enzyme-linked immunosorbent assay kit was used to measure OPG values. Left or right ABI values of <0.9 were categorized as the low ABI group. Among 70 patients on PD, 13 (18.6%) were categorized in the low ABI group. Patients in the low ABI group had higher prevalence of diabetes mellitus (p = .044) and higher serum C-reactive protein (CRP) (p < .001) and OPG levels (p < .001) but lower creatinine (p = .013) and peritoneal Kt/V (p = .048) levels than those in the normal ABI group. Results of multivariable logistic regression analysis revealed that OPG [adjusted odds ratio (aOR) 1.027, 95% confidence interval (CI) 1.010–1.045, p = .002] and CRP (aOR 1.102, 95% CI 1.006–1.207, p = .037) levels were independent predictors of PAD in patients on PD. OPG can also be used to predict PAD development with the area under the receiver operating characteristic curve of 0.823 (95% CI: 0.714–0.904, p < .001) in patients on PD. Therefore, serum OPG and CRP levels can be considered as risk factors for PAD development in patients on PD. |
format | Online Article Text |
id | pubmed-7006676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-70066762020-02-20 Serum osteoprotegerin level is positively associated with peripheral artery disease in patients with peritoneal dialysis Lin, Wei-Chen Tsai, Jen-Pi Lai, Yu-Hsien Lin, Yu-Li Kuo, Chiu-Huang Wang, Chih-Hsien Hsu, Bang-Gee Ren Fail Clinical Study Osteoprotegerin (OPG) is a potential biomarker of cardiovascular disease complications and severity. Peripheral arterial disease (PAD) is associated with an increased risk of death in patients on peritoneal dialysis (PD). Therefore, this study aimed to evaluate the relationship between serum OPG levels and PAD by measuring the ankle-brachial index (ABI) of patients on PD. A commercial enzyme-linked immunosorbent assay kit was used to measure OPG values. Left or right ABI values of <0.9 were categorized as the low ABI group. Among 70 patients on PD, 13 (18.6%) were categorized in the low ABI group. Patients in the low ABI group had higher prevalence of diabetes mellitus (p = .044) and higher serum C-reactive protein (CRP) (p < .001) and OPG levels (p < .001) but lower creatinine (p = .013) and peritoneal Kt/V (p = .048) levels than those in the normal ABI group. Results of multivariable logistic regression analysis revealed that OPG [adjusted odds ratio (aOR) 1.027, 95% confidence interval (CI) 1.010–1.045, p = .002] and CRP (aOR 1.102, 95% CI 1.006–1.207, p = .037) levels were independent predictors of PAD in patients on PD. OPG can also be used to predict PAD development with the area under the receiver operating characteristic curve of 0.823 (95% CI: 0.714–0.904, p < .001) in patients on PD. Therefore, serum OPG and CRP levels can be considered as risk factors for PAD development in patients on PD. Taylor & Francis 2020-01-17 /pmc/articles/PMC7006676/ /pubmed/31950864 http://dx.doi.org/10.1080/0886022X.2020.1714654 Text en © 2020 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 Lin, Wei-Chen Tsai, Jen-Pi Lai, Yu-Hsien Lin, Yu-Li Kuo, Chiu-Huang Wang, Chih-Hsien Hsu, Bang-Gee Serum osteoprotegerin level is positively associated with peripheral artery disease in patients with peritoneal dialysis |
title | Serum osteoprotegerin level is positively associated with peripheral artery disease in patients with peritoneal dialysis |
title_full | Serum osteoprotegerin level is positively associated with peripheral artery disease in patients with peritoneal dialysis |
title_fullStr | Serum osteoprotegerin level is positively associated with peripheral artery disease in patients with peritoneal dialysis |
title_full_unstemmed | Serum osteoprotegerin level is positively associated with peripheral artery disease in patients with peritoneal dialysis |
title_short | Serum osteoprotegerin level is positively associated with peripheral artery disease in patients with peritoneal dialysis |
title_sort | serum osteoprotegerin level is positively associated with peripheral artery disease in patients with peritoneal dialysis |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006676/ https://www.ncbi.nlm.nih.gov/pubmed/31950864 http://dx.doi.org/10.1080/0886022X.2020.1714654 |
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