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Low 25-Hydroxyvitamin D Levels Are Associated with Infections and Mortality in Patients with Cirrhosis

BACKGROUND & AIMS: Vitamin D, best known to regulate bone mineralization, has numerous additional roles including regulation inflammatory pathways. Recently, an increased incidence of 25-hydroxyvitamin D3 (25(OH)D(3)) deficiency has been found in subjects suffering from liver diseases. We here i...

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Autores principales: Finkelmeier, Fabian, Kronenberger, Bernd, Zeuzem, Stefan, Piiper, Albrecht, Waidmann, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487892/
https://www.ncbi.nlm.nih.gov/pubmed/26121590
http://dx.doi.org/10.1371/journal.pone.0132119
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author Finkelmeier, Fabian
Kronenberger, Bernd
Zeuzem, Stefan
Piiper, Albrecht
Waidmann, Oliver
author_facet Finkelmeier, Fabian
Kronenberger, Bernd
Zeuzem, Stefan
Piiper, Albrecht
Waidmann, Oliver
author_sort Finkelmeier, Fabian
collection PubMed
description BACKGROUND & AIMS: Vitamin D, best known to regulate bone mineralization, has numerous additional roles including regulation inflammatory pathways. Recently, an increased incidence of 25-hydroxyvitamin D3 (25(OH)D(3)) deficiency has been found in subjects suffering from liver diseases. We here investigated if low vitamin D levels might be associated with prognosis, inflammation and infectious complications in patients with cirrhosis. METHODS: We performed a prospective cohort study investigating the relation between 25(OH)D(3) levels and stages of cirrhosis, mortality and complications of cirrhosis, including infections. RESULTS: 251 patients with cirrhosis were enrolled into the present prospective cohort study. 25(OH)D(3) levels were quantified by radioimmunoassay from serum samples obtained at study inclusion. The mean follow-up time was 411 ± 397 days with a range of 1-1382 days. 30 (12.0%) patients underwent liver transplantation and 85 (33.8%) individuals died within the study. The mean serum 25(OH)D(3) concentration was 8.93 ± 7.1 ng/ml with a range of 1.0 to 46.0 ng/ml. 25(OH)D(3) levels differed significantly between Child Pugh scores and showed a negative correlation with the model of end stage liver disease (MELD) score. Patients with decompensated cirrhosis and infectious complications, had significantly lower 25(OH)D(3) levels compared to subjects without complications. Low 25(OH)D(3) was associated with mortality in uni- as well as multivariate Cox regression models. CONCLUSIONS: 25(OH)D(3) deficiency is associated with advanced liver disease and low 25(OH)D(3) levels are an indicator for a poor outcome and are associated with infectious complications.
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spelling pubmed-44878922015-07-02 Low 25-Hydroxyvitamin D Levels Are Associated with Infections and Mortality in Patients with Cirrhosis Finkelmeier, Fabian Kronenberger, Bernd Zeuzem, Stefan Piiper, Albrecht Waidmann, Oliver PLoS One Research Article BACKGROUND & AIMS: Vitamin D, best known to regulate bone mineralization, has numerous additional roles including regulation inflammatory pathways. Recently, an increased incidence of 25-hydroxyvitamin D3 (25(OH)D(3)) deficiency has been found in subjects suffering from liver diseases. We here investigated if low vitamin D levels might be associated with prognosis, inflammation and infectious complications in patients with cirrhosis. METHODS: We performed a prospective cohort study investigating the relation between 25(OH)D(3) levels and stages of cirrhosis, mortality and complications of cirrhosis, including infections. RESULTS: 251 patients with cirrhosis were enrolled into the present prospective cohort study. 25(OH)D(3) levels were quantified by radioimmunoassay from serum samples obtained at study inclusion. The mean follow-up time was 411 ± 397 days with a range of 1-1382 days. 30 (12.0%) patients underwent liver transplantation and 85 (33.8%) individuals died within the study. The mean serum 25(OH)D(3) concentration was 8.93 ± 7.1 ng/ml with a range of 1.0 to 46.0 ng/ml. 25(OH)D(3) levels differed significantly between Child Pugh scores and showed a negative correlation with the model of end stage liver disease (MELD) score. Patients with decompensated cirrhosis and infectious complications, had significantly lower 25(OH)D(3) levels compared to subjects without complications. Low 25(OH)D(3) was associated with mortality in uni- as well as multivariate Cox regression models. CONCLUSIONS: 25(OH)D(3) deficiency is associated with advanced liver disease and low 25(OH)D(3) levels are an indicator for a poor outcome and are associated with infectious complications. Public Library of Science 2015-06-29 /pmc/articles/PMC4487892/ /pubmed/26121590 http://dx.doi.org/10.1371/journal.pone.0132119 Text en © 2015 Finkelmeier et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Finkelmeier, Fabian
Kronenberger, Bernd
Zeuzem, Stefan
Piiper, Albrecht
Waidmann, Oliver
Low 25-Hydroxyvitamin D Levels Are Associated with Infections and Mortality in Patients with Cirrhosis
title Low 25-Hydroxyvitamin D Levels Are Associated with Infections and Mortality in Patients with Cirrhosis
title_full Low 25-Hydroxyvitamin D Levels Are Associated with Infections and Mortality in Patients with Cirrhosis
title_fullStr Low 25-Hydroxyvitamin D Levels Are Associated with Infections and Mortality in Patients with Cirrhosis
title_full_unstemmed Low 25-Hydroxyvitamin D Levels Are Associated with Infections and Mortality in Patients with Cirrhosis
title_short Low 25-Hydroxyvitamin D Levels Are Associated with Infections and Mortality in Patients with Cirrhosis
title_sort low 25-hydroxyvitamin d levels are associated with infections and mortality in patients with cirrhosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487892/
https://www.ncbi.nlm.nih.gov/pubmed/26121590
http://dx.doi.org/10.1371/journal.pone.0132119
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