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Oxidative Stress as Estimated by Gamma-Glutamyl Transferase Levels Amplifies the Alkaline Phosphatase-Dependent Risk for Mortality in ESKD Patients on Dialysis

Alkaline phosphatase (Alk-Phos) is a powerful predictor of death in patients with end-stage kidney disease (ESKD) and oxidative stress is a strong inducer of Alk-Phos in various tissues. We tested the hypothesis that oxidative stress, as estimated by a robust marker of systemic oxidative stress like...

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Autores principales: Torino, Claudia, Mattace-Raso, Francesco, van Saase, Jan L. C. M., Postorino, Maurizio, Tripepi, Giovanni Luigi, Mallamaci, Francesca, Zoccali, Carmine, PROGREDIRE Study Group
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976170/
https://www.ncbi.nlm.nih.gov/pubmed/27525053
http://dx.doi.org/10.1155/2016/8490643
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author Torino, Claudia
Mattace-Raso, Francesco
van Saase, Jan L. C. M.
Postorino, Maurizio
Tripepi, Giovanni Luigi
Mallamaci, Francesca
Zoccali, Carmine
PROGREDIRE Study Group,
author_facet Torino, Claudia
Mattace-Raso, Francesco
van Saase, Jan L. C. M.
Postorino, Maurizio
Tripepi, Giovanni Luigi
Mallamaci, Francesca
Zoccali, Carmine
PROGREDIRE Study Group,
author_sort Torino, Claudia
collection PubMed
description Alkaline phosphatase (Alk-Phos) is a powerful predictor of death in patients with end-stage kidney disease (ESKD) and oxidative stress is a strong inducer of Alk-Phos in various tissues. We tested the hypothesis that oxidative stress, as estimated by a robust marker of systemic oxidative stress like γ-Glutamyl-Transpeptidase (GGT) levels, may interact with Alk-Phos in the high risk of death in a cohort of 993 ESKD patients maintained on chronic dialysis. In fully adjusted analyses the HR for mortality associated with Alk-Phos (50 IU/L increase) was progressively higher across GGT quintiles, being minimal in patients in the first quintile (HR: 0.89, 95% CI: 0.77–1.03) and highest in the GGT fifth quintile (HR: 1.13, 95% CI: 1.03–1.2) (P for the effect modification = 0.02). These findings were fully confirmed in sensitivity analyses excluding patients with preexisting liver disease, excessive alcohol intake, or altered liver disease biomarkers. GGT amplifies the risk of death associated with high Alk-Phos levels in ESKD patients. This observation is compatible with the hypothesis that oxidative stress is a strong modifier of the adverse biological effects of high Alk-Phos in this population.
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spelling pubmed-49761702016-08-14 Oxidative Stress as Estimated by Gamma-Glutamyl Transferase Levels Amplifies the Alkaline Phosphatase-Dependent Risk for Mortality in ESKD Patients on Dialysis Torino, Claudia Mattace-Raso, Francesco van Saase, Jan L. C. M. Postorino, Maurizio Tripepi, Giovanni Luigi Mallamaci, Francesca Zoccali, Carmine PROGREDIRE Study Group, Oxid Med Cell Longev Research Article Alkaline phosphatase (Alk-Phos) is a powerful predictor of death in patients with end-stage kidney disease (ESKD) and oxidative stress is a strong inducer of Alk-Phos in various tissues. We tested the hypothesis that oxidative stress, as estimated by a robust marker of systemic oxidative stress like γ-Glutamyl-Transpeptidase (GGT) levels, may interact with Alk-Phos in the high risk of death in a cohort of 993 ESKD patients maintained on chronic dialysis. In fully adjusted analyses the HR for mortality associated with Alk-Phos (50 IU/L increase) was progressively higher across GGT quintiles, being minimal in patients in the first quintile (HR: 0.89, 95% CI: 0.77–1.03) and highest in the GGT fifth quintile (HR: 1.13, 95% CI: 1.03–1.2) (P for the effect modification = 0.02). These findings were fully confirmed in sensitivity analyses excluding patients with preexisting liver disease, excessive alcohol intake, or altered liver disease biomarkers. GGT amplifies the risk of death associated with high Alk-Phos levels in ESKD patients. This observation is compatible with the hypothesis that oxidative stress is a strong modifier of the adverse biological effects of high Alk-Phos in this population. Hindawi Publishing Corporation 2016 2016-07-25 /pmc/articles/PMC4976170/ /pubmed/27525053 http://dx.doi.org/10.1155/2016/8490643 Text en Copyright © 2016 Claudia Torino et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Torino, Claudia
Mattace-Raso, Francesco
van Saase, Jan L. C. M.
Postorino, Maurizio
Tripepi, Giovanni Luigi
Mallamaci, Francesca
Zoccali, Carmine
PROGREDIRE Study Group,
Oxidative Stress as Estimated by Gamma-Glutamyl Transferase Levels Amplifies the Alkaline Phosphatase-Dependent Risk for Mortality in ESKD Patients on Dialysis
title Oxidative Stress as Estimated by Gamma-Glutamyl Transferase Levels Amplifies the Alkaline Phosphatase-Dependent Risk for Mortality in ESKD Patients on Dialysis
title_full Oxidative Stress as Estimated by Gamma-Glutamyl Transferase Levels Amplifies the Alkaline Phosphatase-Dependent Risk for Mortality in ESKD Patients on Dialysis
title_fullStr Oxidative Stress as Estimated by Gamma-Glutamyl Transferase Levels Amplifies the Alkaline Phosphatase-Dependent Risk for Mortality in ESKD Patients on Dialysis
title_full_unstemmed Oxidative Stress as Estimated by Gamma-Glutamyl Transferase Levels Amplifies the Alkaline Phosphatase-Dependent Risk for Mortality in ESKD Patients on Dialysis
title_short Oxidative Stress as Estimated by Gamma-Glutamyl Transferase Levels Amplifies the Alkaline Phosphatase-Dependent Risk for Mortality in ESKD Patients on Dialysis
title_sort oxidative stress as estimated by gamma-glutamyl transferase levels amplifies the alkaline phosphatase-dependent risk for mortality in eskd patients on dialysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976170/
https://www.ncbi.nlm.nih.gov/pubmed/27525053
http://dx.doi.org/10.1155/2016/8490643
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