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Serum sclerostin is an independent predictor of mortality in hemodialysis patients
BACKGROUND: Sclerostin (Scl) has recently emerged as a novel marker of bone remodeling and vascular calcification. However, whether high circulating Scl is also a risk factor for death is not well established. The purpose of this study was to test whether serum Scl would be associated with mortality...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265422/ https://www.ncbi.nlm.nih.gov/pubmed/25465028 http://dx.doi.org/10.1186/1471-2369-15-190 |
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author | Gonçalves, Flávia Letícia Carvalho Elias, Rosilene M dos Reis, Luciene M Graciolli, Fabiana G Zampieri, Fernando Godinho Oliveira, Rodrigo B Jorgetti, Vanda Moysés, Rosa MA |
author_facet | Gonçalves, Flávia Letícia Carvalho Elias, Rosilene M dos Reis, Luciene M Graciolli, Fabiana G Zampieri, Fernando Godinho Oliveira, Rodrigo B Jorgetti, Vanda Moysés, Rosa MA |
author_sort | Gonçalves, Flávia Letícia Carvalho |
collection | PubMed |
description | BACKGROUND: Sclerostin (Scl) has recently emerged as a novel marker of bone remodeling and vascular calcification. However, whether high circulating Scl is also a risk factor for death is not well established. The purpose of this study was to test whether serum Scl would be associated with mortality. METHODS: we measured serum Scl in a hemodialysis patients’ cohort, which was followed during a ten-year period. Competing risk regression models were applied, as during the follow-up, patients were exposed to both events kidney transplant and death. RESULTS: Ninety-one patients aged 42.3 ± 18.8 years (55% of male gender, 15% of diabetes) were included. During the follow-up, 32 patients underwent kidney transplant and 26 patients died. Non-survivals presented higher FGF23, higher Scl and lower creatinine. There was an association between all-cause mortality and higher Scl (HR = 2.2), higher age (HR = 1.04) and presence of diabetes (HR = 2.27), by competing risk analyses. Even including potential markers of mortality, as creatinine, FGF 23, and gender, Scl, age and diabetes remained significantly related to higher mortality. CONCLUSION: Serum Scl is an independent predictor of mortality in dialysis patients. However, whether clinical interventions to modulate Scl would be able to improve these patients survival needs to be determined. |
format | Online Article Text |
id | pubmed-4265422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42654222014-12-15 Serum sclerostin is an independent predictor of mortality in hemodialysis patients Gonçalves, Flávia Letícia Carvalho Elias, Rosilene M dos Reis, Luciene M Graciolli, Fabiana G Zampieri, Fernando Godinho Oliveira, Rodrigo B Jorgetti, Vanda Moysés, Rosa MA BMC Nephrol Research Article BACKGROUND: Sclerostin (Scl) has recently emerged as a novel marker of bone remodeling and vascular calcification. However, whether high circulating Scl is also a risk factor for death is not well established. The purpose of this study was to test whether serum Scl would be associated with mortality. METHODS: we measured serum Scl in a hemodialysis patients’ cohort, which was followed during a ten-year period. Competing risk regression models were applied, as during the follow-up, patients were exposed to both events kidney transplant and death. RESULTS: Ninety-one patients aged 42.3 ± 18.8 years (55% of male gender, 15% of diabetes) were included. During the follow-up, 32 patients underwent kidney transplant and 26 patients died. Non-survivals presented higher FGF23, higher Scl and lower creatinine. There was an association between all-cause mortality and higher Scl (HR = 2.2), higher age (HR = 1.04) and presence of diabetes (HR = 2.27), by competing risk analyses. Even including potential markers of mortality, as creatinine, FGF 23, and gender, Scl, age and diabetes remained significantly related to higher mortality. CONCLUSION: Serum Scl is an independent predictor of mortality in dialysis patients. However, whether clinical interventions to modulate Scl would be able to improve these patients survival needs to be determined. BioMed Central 2014-12-02 /pmc/articles/PMC4265422/ /pubmed/25465028 http://dx.doi.org/10.1186/1471-2369-15-190 Text en © Gonçalves et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Gonçalves, Flávia Letícia Carvalho Elias, Rosilene M dos Reis, Luciene M Graciolli, Fabiana G Zampieri, Fernando Godinho Oliveira, Rodrigo B Jorgetti, Vanda Moysés, Rosa MA Serum sclerostin is an independent predictor of mortality in hemodialysis patients |
title | Serum sclerostin is an independent predictor of mortality in hemodialysis patients |
title_full | Serum sclerostin is an independent predictor of mortality in hemodialysis patients |
title_fullStr | Serum sclerostin is an independent predictor of mortality in hemodialysis patients |
title_full_unstemmed | Serum sclerostin is an independent predictor of mortality in hemodialysis patients |
title_short | Serum sclerostin is an independent predictor of mortality in hemodialysis patients |
title_sort | serum sclerostin is an independent predictor of mortality in hemodialysis patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265422/ https://www.ncbi.nlm.nih.gov/pubmed/25465028 http://dx.doi.org/10.1186/1471-2369-15-190 |
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