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Relationship of Fibroblast Growth Factor 23 With Hospitalization for Heart Failure and Cardiovascular Outcomes in Patients Undergoing Cardiac Surgery

BACKGROUND: Fibroblast growth factor 23 (FGF‐23) is crucial in regulating phosphate and vitamin D metabolism and is moreover associated with an increased cardiovascular risk. The specific objective of this study was to investigate the influence of FGF‐23 on cardiovascular outcomes, including hospita...

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Autores principales: Hofer, Felix, Hammer, Andreas, Pailer, Ulrike, Koller, Lorenz, Kazem, Niema, Steinacher, Eva, Steinlechner, Barbara, Andreas, Martin, Laufer, Günther, Wojta, Johann, Zelniker, Thomas A., Hengstenberg, Christian, Niessner, Alexander, Sulzgruber, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10111457/
https://www.ncbi.nlm.nih.gov/pubmed/36802737
http://dx.doi.org/10.1161/JAHA.122.027875
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author Hofer, Felix
Hammer, Andreas
Pailer, Ulrike
Koller, Lorenz
Kazem, Niema
Steinacher, Eva
Steinlechner, Barbara
Andreas, Martin
Laufer, Günther
Wojta, Johann
Zelniker, Thomas A.
Hengstenberg, Christian
Niessner, Alexander
Sulzgruber, Patrick
author_facet Hofer, Felix
Hammer, Andreas
Pailer, Ulrike
Koller, Lorenz
Kazem, Niema
Steinacher, Eva
Steinlechner, Barbara
Andreas, Martin
Laufer, Günther
Wojta, Johann
Zelniker, Thomas A.
Hengstenberg, Christian
Niessner, Alexander
Sulzgruber, Patrick
author_sort Hofer, Felix
collection PubMed
description BACKGROUND: Fibroblast growth factor 23 (FGF‐23) is crucial in regulating phosphate and vitamin D metabolism and is moreover associated with an increased cardiovascular risk. The specific objective of this study was to investigate the influence of FGF‐23 on cardiovascular outcomes, including hospitalization for heart failure (HHF), postoperative atrial fibrillation, and cardiovascular death, in an unselected patient population after cardiac surgery. METHODS AND RESULTS: Patients undergoing elective coronary artery bypass graft and/or cardiac valve surgery were prospectively enrolled. FGF‐23 blood plasma concentrations were assessed before surgery. A composite of cardiovascular death/HHF was chosen as primary end point. A total of 451 patients (median age 70 years; 28.8% female) were included in the present analysis and followed over a median of 3.9 years. Individuals with higher FGF‐23 quartiles showed elevated incidence rates of the composite of cardiovascular death/HHF (quartile 1, 7.1%; quartile 2, 8.6%; quartile 3, 15.1%; and quartile 4, 34.3%). After multivariable adjustment, FGF‐23 modeled as a continuous variable (adjusted hazard ratio for a 1‐unit increase in standardized log‐transformed biomarker, 1.82 [95% CI, 1.34–2.46]) as well as using predefined risk groups and quartiles remained independently associated with the risk of cardiovascular death/HHF and the secondary outcomes, including postoperative atrial fibrillation. Reclassification analysis indicated that the addition of FGF‐23 to N‐terminal pro‐B‐type natriuretic peptide provides a significant improvement in risk discrimination (net reclassification improvement at the event rate, 0.58 [95% CI, 0.34–0.81]; P<0.001; integrated discrimination increment, 0.03 [95% CI, 0.01–0.05]; P<0.001). CONCLUSIONS: FGF‐23 is an independent predictor of cardiovascular death/HHF and postoperative atrial fibrillation in individuals undergoing cardiac surgery. Considering an individualized risk assessment, routine preoperative FGF‐23 evaluation may improve detection of high‐risk patients.
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spelling pubmed-101114572023-04-19 Relationship of Fibroblast Growth Factor 23 With Hospitalization for Heart Failure and Cardiovascular Outcomes in Patients Undergoing Cardiac Surgery Hofer, Felix Hammer, Andreas Pailer, Ulrike Koller, Lorenz Kazem, Niema Steinacher, Eva Steinlechner, Barbara Andreas, Martin Laufer, Günther Wojta, Johann Zelniker, Thomas A. Hengstenberg, Christian Niessner, Alexander Sulzgruber, Patrick J Am Heart Assoc Original Research BACKGROUND: Fibroblast growth factor 23 (FGF‐23) is crucial in regulating phosphate and vitamin D metabolism and is moreover associated with an increased cardiovascular risk. The specific objective of this study was to investigate the influence of FGF‐23 on cardiovascular outcomes, including hospitalization for heart failure (HHF), postoperative atrial fibrillation, and cardiovascular death, in an unselected patient population after cardiac surgery. METHODS AND RESULTS: Patients undergoing elective coronary artery bypass graft and/or cardiac valve surgery were prospectively enrolled. FGF‐23 blood plasma concentrations were assessed before surgery. A composite of cardiovascular death/HHF was chosen as primary end point. A total of 451 patients (median age 70 years; 28.8% female) were included in the present analysis and followed over a median of 3.9 years. Individuals with higher FGF‐23 quartiles showed elevated incidence rates of the composite of cardiovascular death/HHF (quartile 1, 7.1%; quartile 2, 8.6%; quartile 3, 15.1%; and quartile 4, 34.3%). After multivariable adjustment, FGF‐23 modeled as a continuous variable (adjusted hazard ratio for a 1‐unit increase in standardized log‐transformed biomarker, 1.82 [95% CI, 1.34–2.46]) as well as using predefined risk groups and quartiles remained independently associated with the risk of cardiovascular death/HHF and the secondary outcomes, including postoperative atrial fibrillation. Reclassification analysis indicated that the addition of FGF‐23 to N‐terminal pro‐B‐type natriuretic peptide provides a significant improvement in risk discrimination (net reclassification improvement at the event rate, 0.58 [95% CI, 0.34–0.81]; P<0.001; integrated discrimination increment, 0.03 [95% CI, 0.01–0.05]; P<0.001). CONCLUSIONS: FGF‐23 is an independent predictor of cardiovascular death/HHF and postoperative atrial fibrillation in individuals undergoing cardiac surgery. Considering an individualized risk assessment, routine preoperative FGF‐23 evaluation may improve detection of high‐risk patients. John Wiley and Sons Inc. 2023-02-21 /pmc/articles/PMC10111457/ /pubmed/36802737 http://dx.doi.org/10.1161/JAHA.122.027875 Text en © 2023 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Hofer, Felix
Hammer, Andreas
Pailer, Ulrike
Koller, Lorenz
Kazem, Niema
Steinacher, Eva
Steinlechner, Barbara
Andreas, Martin
Laufer, Günther
Wojta, Johann
Zelniker, Thomas A.
Hengstenberg, Christian
Niessner, Alexander
Sulzgruber, Patrick
Relationship of Fibroblast Growth Factor 23 With Hospitalization for Heart Failure and Cardiovascular Outcomes in Patients Undergoing Cardiac Surgery
title Relationship of Fibroblast Growth Factor 23 With Hospitalization for Heart Failure and Cardiovascular Outcomes in Patients Undergoing Cardiac Surgery
title_full Relationship of Fibroblast Growth Factor 23 With Hospitalization for Heart Failure and Cardiovascular Outcomes in Patients Undergoing Cardiac Surgery
title_fullStr Relationship of Fibroblast Growth Factor 23 With Hospitalization for Heart Failure and Cardiovascular Outcomes in Patients Undergoing Cardiac Surgery
title_full_unstemmed Relationship of Fibroblast Growth Factor 23 With Hospitalization for Heart Failure and Cardiovascular Outcomes in Patients Undergoing Cardiac Surgery
title_short Relationship of Fibroblast Growth Factor 23 With Hospitalization for Heart Failure and Cardiovascular Outcomes in Patients Undergoing Cardiac Surgery
title_sort relationship of fibroblast growth factor 23 with hospitalization for heart failure and cardiovascular outcomes in patients undergoing cardiac surgery
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10111457/
https://www.ncbi.nlm.nih.gov/pubmed/36802737
http://dx.doi.org/10.1161/JAHA.122.027875
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