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Paricalcitol reduces oxidative stress and inflammation in hemodialysis patients

BACKGROUND: Treatment with selective vitamin D receptor activators such as paricalcitol have been shown to exert an anti-inflammatory effect in patients on hemodialysis, in addition to their action on mineral metabolism and independently of parathyroid hormone (PTH) levels. The objective of this stu...

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Autores principales: Izquierdo, María Jesús, Cavia, Mónica, Muñiz, Pilar, de Francisco, Angel LM, Arias, Manuel, Santos, Javier, Abaigar, Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520723/
https://www.ncbi.nlm.nih.gov/pubmed/23186077
http://dx.doi.org/10.1186/1471-2369-13-159
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author Izquierdo, María Jesús
Cavia, Mónica
Muñiz, Pilar
de Francisco, Angel LM
Arias, Manuel
Santos, Javier
Abaigar, Pedro
author_facet Izquierdo, María Jesús
Cavia, Mónica
Muñiz, Pilar
de Francisco, Angel LM
Arias, Manuel
Santos, Javier
Abaigar, Pedro
author_sort Izquierdo, María Jesús
collection PubMed
description BACKGROUND: Treatment with selective vitamin D receptor activators such as paricalcitol have been shown to exert an anti-inflammatory effect in patients on hemodialysis, in addition to their action on mineral metabolism and independently of parathyroid hormone (PTH) levels. The objective of this study was to evaluate the additional antioxidant capacity of paricalcitol in a clinical setting. METHODS: The study included 19 patients with renal disease on hemodialysis, of whom peripheral blood was obtained for analysis at baseline and three months after starting intravenous paricalcitol treatment. The following oxidizing and inflammatory markers were quantified: malondialdehyde (MDA), nitrites and carbonyl groups, indoleamine 2,3-dioxygenase (IDO), tumor necrosis factor alfa (TNF-α), interleukin-6 (IL-6), interleukin-18 (IL-18) and C-reactive protein (CRP). Of the antioxidants and anti-inflammatory markers, superoxide dismutase (SOD), catalase, reduced glutathione (GSH), thioredoxin, and interleukin-10 (IL-10) levels were obtained. RESULTS: Baseline levels of oxidation markers MDA, nitric oxide and protein carbonyl groups significantly decreased after three months on paricalcitol treatment, while levels of GSH, thioredoxin, catalase and SOD activity significantly increased. After paricalcitol treatment, levels of the inflammatory markers CRP, TNF-α, IL-6 and IL-18 were significantly reduced in serum and the level of anti-inflammatory cytokine IL-10 was increased. CONCLUSIONS: In renal patients undergoing hemodialysis, paricalcitol treatment significantly reduces oxidative stress and inflammation, two well known factors leading to cardiovascular damage.
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spelling pubmed-35207232012-12-13 Paricalcitol reduces oxidative stress and inflammation in hemodialysis patients Izquierdo, María Jesús Cavia, Mónica Muñiz, Pilar de Francisco, Angel LM Arias, Manuel Santos, Javier Abaigar, Pedro BMC Nephrol Research Article BACKGROUND: Treatment with selective vitamin D receptor activators such as paricalcitol have been shown to exert an anti-inflammatory effect in patients on hemodialysis, in addition to their action on mineral metabolism and independently of parathyroid hormone (PTH) levels. The objective of this study was to evaluate the additional antioxidant capacity of paricalcitol in a clinical setting. METHODS: The study included 19 patients with renal disease on hemodialysis, of whom peripheral blood was obtained for analysis at baseline and three months after starting intravenous paricalcitol treatment. The following oxidizing and inflammatory markers were quantified: malondialdehyde (MDA), nitrites and carbonyl groups, indoleamine 2,3-dioxygenase (IDO), tumor necrosis factor alfa (TNF-α), interleukin-6 (IL-6), interleukin-18 (IL-18) and C-reactive protein (CRP). Of the antioxidants and anti-inflammatory markers, superoxide dismutase (SOD), catalase, reduced glutathione (GSH), thioredoxin, and interleukin-10 (IL-10) levels were obtained. RESULTS: Baseline levels of oxidation markers MDA, nitric oxide and protein carbonyl groups significantly decreased after three months on paricalcitol treatment, while levels of GSH, thioredoxin, catalase and SOD activity significantly increased. After paricalcitol treatment, levels of the inflammatory markers CRP, TNF-α, IL-6 and IL-18 were significantly reduced in serum and the level of anti-inflammatory cytokine IL-10 was increased. CONCLUSIONS: In renal patients undergoing hemodialysis, paricalcitol treatment significantly reduces oxidative stress and inflammation, two well known factors leading to cardiovascular damage. BioMed Central 2012-11-27 /pmc/articles/PMC3520723/ /pubmed/23186077 http://dx.doi.org/10.1186/1471-2369-13-159 Text en Copyright ©2012 Izquierdo et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Izquierdo, María Jesús
Cavia, Mónica
Muñiz, Pilar
de Francisco, Angel LM
Arias, Manuel
Santos, Javier
Abaigar, Pedro
Paricalcitol reduces oxidative stress and inflammation in hemodialysis patients
title Paricalcitol reduces oxidative stress and inflammation in hemodialysis patients
title_full Paricalcitol reduces oxidative stress and inflammation in hemodialysis patients
title_fullStr Paricalcitol reduces oxidative stress and inflammation in hemodialysis patients
title_full_unstemmed Paricalcitol reduces oxidative stress and inflammation in hemodialysis patients
title_short Paricalcitol reduces oxidative stress and inflammation in hemodialysis patients
title_sort paricalcitol reduces oxidative stress and inflammation in hemodialysis patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520723/
https://www.ncbi.nlm.nih.gov/pubmed/23186077
http://dx.doi.org/10.1186/1471-2369-13-159
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