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Ceruloplasmin as Redox Marker Related to Heart Failure Severity

This study examined ceruloplasmin levels in patients with HFrEF, depending on cardiopulmonary exercise testing (CPET) parameters; a correlation was found between ceruloplasmin (CER) and iron and hepatic status, inflammatory and redox biomarkers. A group of 552 patients was divided according to Weber...

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Autores principales: Lazar-Poloczek, Elżbieta, Romuk, Ewa, Rozentryt, Piotr, Duda, Sylwia, Gąsior, Mariusz, Wojciechowska, Celina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467566/
https://www.ncbi.nlm.nih.gov/pubmed/34576235
http://dx.doi.org/10.3390/ijms221810074
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author Lazar-Poloczek, Elżbieta
Romuk, Ewa
Rozentryt, Piotr
Duda, Sylwia
Gąsior, Mariusz
Wojciechowska, Celina
author_facet Lazar-Poloczek, Elżbieta
Romuk, Ewa
Rozentryt, Piotr
Duda, Sylwia
Gąsior, Mariusz
Wojciechowska, Celina
author_sort Lazar-Poloczek, Elżbieta
collection PubMed
description This study examined ceruloplasmin levels in patients with HFrEF, depending on cardiopulmonary exercise testing (CPET) parameters; a correlation was found between ceruloplasmin (CER) and iron and hepatic status, inflammatory and redox biomarkers. A group of 552 patients was divided according to Weber’s classification: there were 72 (13%) patients in class A (peak VO(2) > 20 mL/kg/min), 116 (21%) patients in class B (peak VO(2) 16–20 mL/kg/min), 276 (50%) patients in class C (peak VO(2) 10–15.9 mL/kg/min) and 88 (16%) patients in class D (peak VO(2) < 10 mL/kg/min). A higher concentration of CER was found in patients with peak VO(2) < 16 mL/kg/min and VE/CO(2) slope > 45 compared to patients with VE/CO(2) slope < 45 (escectively CER 30.6 mg/dL and 27.5 mg/dL). A significantly positive correlation was found between ceruloplasmin and NYHA class, RV diameter, NT-proBNP, uric acid, total protein, fibrinogen and hepatic enzymes. CER was positively correlated with both total oxidant status (TOS), total antioxidant capacity (TAC) and malondialdehyde. A model constructed to predict CER concentration indicated that TOS, malondialdehyde and alkaline phosphatase were independent predictive variables (R(2) 0.14, p < 0.001). CER as a continuous variable was an independent predictor of pVO(2) ≤ 12 mL/kg/min after adjustment for sex, age and BMI. These results provide the basis of a new classification to encourage the determination of CER as a useful biomarker in HFrEF.
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spelling pubmed-84675662021-09-27 Ceruloplasmin as Redox Marker Related to Heart Failure Severity Lazar-Poloczek, Elżbieta Romuk, Ewa Rozentryt, Piotr Duda, Sylwia Gąsior, Mariusz Wojciechowska, Celina Int J Mol Sci Article This study examined ceruloplasmin levels in patients with HFrEF, depending on cardiopulmonary exercise testing (CPET) parameters; a correlation was found between ceruloplasmin (CER) and iron and hepatic status, inflammatory and redox biomarkers. A group of 552 patients was divided according to Weber’s classification: there were 72 (13%) patients in class A (peak VO(2) > 20 mL/kg/min), 116 (21%) patients in class B (peak VO(2) 16–20 mL/kg/min), 276 (50%) patients in class C (peak VO(2) 10–15.9 mL/kg/min) and 88 (16%) patients in class D (peak VO(2) < 10 mL/kg/min). A higher concentration of CER was found in patients with peak VO(2) < 16 mL/kg/min and VE/CO(2) slope > 45 compared to patients with VE/CO(2) slope < 45 (escectively CER 30.6 mg/dL and 27.5 mg/dL). A significantly positive correlation was found between ceruloplasmin and NYHA class, RV diameter, NT-proBNP, uric acid, total protein, fibrinogen and hepatic enzymes. CER was positively correlated with both total oxidant status (TOS), total antioxidant capacity (TAC) and malondialdehyde. A model constructed to predict CER concentration indicated that TOS, malondialdehyde and alkaline phosphatase were independent predictive variables (R(2) 0.14, p < 0.001). CER as a continuous variable was an independent predictor of pVO(2) ≤ 12 mL/kg/min after adjustment for sex, age and BMI. These results provide the basis of a new classification to encourage the determination of CER as a useful biomarker in HFrEF. MDPI 2021-09-17 /pmc/articles/PMC8467566/ /pubmed/34576235 http://dx.doi.org/10.3390/ijms221810074 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lazar-Poloczek, Elżbieta
Romuk, Ewa
Rozentryt, Piotr
Duda, Sylwia
Gąsior, Mariusz
Wojciechowska, Celina
Ceruloplasmin as Redox Marker Related to Heart Failure Severity
title Ceruloplasmin as Redox Marker Related to Heart Failure Severity
title_full Ceruloplasmin as Redox Marker Related to Heart Failure Severity
title_fullStr Ceruloplasmin as Redox Marker Related to Heart Failure Severity
title_full_unstemmed Ceruloplasmin as Redox Marker Related to Heart Failure Severity
title_short Ceruloplasmin as Redox Marker Related to Heart Failure Severity
title_sort ceruloplasmin as redox marker related to heart failure severity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467566/
https://www.ncbi.nlm.nih.gov/pubmed/34576235
http://dx.doi.org/10.3390/ijms221810074
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