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25(OH)D and 1,25(OH)D vitamin D fails to predict sepsis and mortality in a prospective cohort study

The clinical role of vitamin D in sepsis and mortality prediction is controversially discussed. Therefore, we conducted a prospective cohort study on standard care wards, including 461 patients with suspected sepsis fulfilling two or more SIRS criteria. On the first and third day after onset of SIRS...

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Autores principales: Ratzinger, Franz, Haslacher, Helmuth, Stadlberger, Markus, Schmidt, Ralf L. J., Obermüller, Markus, Schmetterer, Klaus G., Perkmann, Thomas, Makristathis, Athanasios, Marculescu, Rodrig, Burgmann, Heinz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5228346/
https://www.ncbi.nlm.nih.gov/pubmed/28079172
http://dx.doi.org/10.1038/srep40646
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author Ratzinger, Franz
Haslacher, Helmuth
Stadlberger, Markus
Schmidt, Ralf L. J.
Obermüller, Markus
Schmetterer, Klaus G.
Perkmann, Thomas
Makristathis, Athanasios
Marculescu, Rodrig
Burgmann, Heinz
author_facet Ratzinger, Franz
Haslacher, Helmuth
Stadlberger, Markus
Schmidt, Ralf L. J.
Obermüller, Markus
Schmetterer, Klaus G.
Perkmann, Thomas
Makristathis, Athanasios
Marculescu, Rodrig
Burgmann, Heinz
author_sort Ratzinger, Franz
collection PubMed
description The clinical role of vitamin D in sepsis and mortality prediction is controversially discussed. Therefore, we conducted a prospective cohort study on standard care wards, including 461 patients with suspected sepsis fulfilling two or more SIRS criteria. On the first and third day after onset of SIRS symptoms levels of 25(OH)D, 1,25(OH)D and sepsis biomarkers were analysed for their predictive capacity for identifying infection, bacteraemia and an elevated mortality risk. Additionally, several SNPs associated with vitamin D metabolism were evaluated. Bacteraemic patients (28.5%) presented with significantly lower 1,25(OH)D levels than SIRS patients without bacteraemia on the first and third day, while 25(OH)D did not show a predictive capacity. No significant differences of either 1,25(OH)D or 25(OH)D levels were found between SIRS patients with and without infections or between survivors and non-survivors. Sepsis biomarkers, including procalcitonin and CRP, showed a significantly higher discriminatory capacity for these classification tasks. The vitamin D metabolism-related SNPs analysed did not indicate any association with our outcome measures. In conclusion, 1,25(OH)D but not 25(OH)D showed a minor discriminatory value for the prediction of bacteraemia that was inferior to CRP and PCT but both failed to predict sepsis and mortality in a prospective cohort of SIRS patients.
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spelling pubmed-52283462017-01-17 25(OH)D and 1,25(OH)D vitamin D fails to predict sepsis and mortality in a prospective cohort study Ratzinger, Franz Haslacher, Helmuth Stadlberger, Markus Schmidt, Ralf L. J. Obermüller, Markus Schmetterer, Klaus G. Perkmann, Thomas Makristathis, Athanasios Marculescu, Rodrig Burgmann, Heinz Sci Rep Article The clinical role of vitamin D in sepsis and mortality prediction is controversially discussed. Therefore, we conducted a prospective cohort study on standard care wards, including 461 patients with suspected sepsis fulfilling two or more SIRS criteria. On the first and third day after onset of SIRS symptoms levels of 25(OH)D, 1,25(OH)D and sepsis biomarkers were analysed for their predictive capacity for identifying infection, bacteraemia and an elevated mortality risk. Additionally, several SNPs associated with vitamin D metabolism were evaluated. Bacteraemic patients (28.5%) presented with significantly lower 1,25(OH)D levels than SIRS patients without bacteraemia on the first and third day, while 25(OH)D did not show a predictive capacity. No significant differences of either 1,25(OH)D or 25(OH)D levels were found between SIRS patients with and without infections or between survivors and non-survivors. Sepsis biomarkers, including procalcitonin and CRP, showed a significantly higher discriminatory capacity for these classification tasks. The vitamin D metabolism-related SNPs analysed did not indicate any association with our outcome measures. In conclusion, 1,25(OH)D but not 25(OH)D showed a minor discriminatory value for the prediction of bacteraemia that was inferior to CRP and PCT but both failed to predict sepsis and mortality in a prospective cohort of SIRS patients. Nature Publishing Group 2017-01-12 /pmc/articles/PMC5228346/ /pubmed/28079172 http://dx.doi.org/10.1038/srep40646 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Ratzinger, Franz
Haslacher, Helmuth
Stadlberger, Markus
Schmidt, Ralf L. J.
Obermüller, Markus
Schmetterer, Klaus G.
Perkmann, Thomas
Makristathis, Athanasios
Marculescu, Rodrig
Burgmann, Heinz
25(OH)D and 1,25(OH)D vitamin D fails to predict sepsis and mortality in a prospective cohort study
title 25(OH)D and 1,25(OH)D vitamin D fails to predict sepsis and mortality in a prospective cohort study
title_full 25(OH)D and 1,25(OH)D vitamin D fails to predict sepsis and mortality in a prospective cohort study
title_fullStr 25(OH)D and 1,25(OH)D vitamin D fails to predict sepsis and mortality in a prospective cohort study
title_full_unstemmed 25(OH)D and 1,25(OH)D vitamin D fails to predict sepsis and mortality in a prospective cohort study
title_short 25(OH)D and 1,25(OH)D vitamin D fails to predict sepsis and mortality in a prospective cohort study
title_sort 25(oh)d and 1,25(oh)d vitamin d fails to predict sepsis and mortality in a prospective cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5228346/
https://www.ncbi.nlm.nih.gov/pubmed/28079172
http://dx.doi.org/10.1038/srep40646
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