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Liver tests and outcomes in heart failure with reduced ejection fraction: findings from DAPA‐HF

AIMS: Reflecting both increased venous pressure and reduced cardiac output, abnormal liver tests are common in patients with severe heart failure and are associated with adverse clinical outcomes. We aimed to investigate the prognostic significance of abnormal liver tests in ambulatory patients with...

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Autores principales: Adamson, Carly, Cowan, Lorna M., de Boer, Rudolf A., Diez, Mirta, Drożdż, Jarosław, Dukát, Andre, Inzucchi, Silvio E., Køber, Lars, Kosiborod, Mikhail N., Ljungman, Charlotta E.A., Martinez, Felipe A., Ponikowski, Piotr, Sabatine, Marc S., Lindholm, Daniel, Bengtsson, Olof, Boulton, David W., Greasley, Peter J., Langkilde, Anna Maria, Sjöstrand, Mikaela, Solomon, Scott D., McMurray, John J.V., Jhund, Pardeep S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805158/
https://www.ncbi.nlm.nih.gov/pubmed/36054568
http://dx.doi.org/10.1002/ejhf.2649
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author Adamson, Carly
Cowan, Lorna M.
de Boer, Rudolf A.
Diez, Mirta
Drożdż, Jarosław
Dukát, Andre
Inzucchi, Silvio E.
Køber, Lars
Kosiborod, Mikhail N.
Ljungman, Charlotta E.A.
Martinez, Felipe A.
Ponikowski, Piotr
Sabatine, Marc S.
Lindholm, Daniel
Bengtsson, Olof
Boulton, David W.
Greasley, Peter J.
Langkilde, Anna Maria
Sjöstrand, Mikaela
Solomon, Scott D.
McMurray, John J.V.
Jhund, Pardeep S.
author_facet Adamson, Carly
Cowan, Lorna M.
de Boer, Rudolf A.
Diez, Mirta
Drożdż, Jarosław
Dukát, Andre
Inzucchi, Silvio E.
Køber, Lars
Kosiborod, Mikhail N.
Ljungman, Charlotta E.A.
Martinez, Felipe A.
Ponikowski, Piotr
Sabatine, Marc S.
Lindholm, Daniel
Bengtsson, Olof
Boulton, David W.
Greasley, Peter J.
Langkilde, Anna Maria
Sjöstrand, Mikaela
Solomon, Scott D.
McMurray, John J.V.
Jhund, Pardeep S.
author_sort Adamson, Carly
collection PubMed
description AIMS: Reflecting both increased venous pressure and reduced cardiac output, abnormal liver tests are common in patients with severe heart failure and are associated with adverse clinical outcomes. We aimed to investigate the prognostic significance of abnormal liver tests in ambulatory patients with heart failure with reduced ejection fraction (HFrEF), explore any treatment interaction between bilirubin and sodium–glucose cotransporter 2 (SGLT2) inhibitors and examine change in liver tests with SGLT2 inhibitor treatment. METHODS AND RESULTS: We explored these objectives in the Dapagliflozin And Prevention of Adverse outcomes in Heart Failure (DAPA‐HF) trial, with focus on bilirubin. We calculated the incidence of cardiovascular death or worsening heart failure by bilirubin tertile. Secondary cardiovascular outcomes were examined, along with the change in liver tests at the end‐of‐study visit. Baseline bilirubin was available in 4720 patients (99.5%). Participants in the highest bilirubin tertile (T3) have more severe HFrEF (lower left ventricular ejection fraction, higher N‐terminal pro‐B‐type natriuretic peptide [NT‐proBNP] and worse New York Heart Association class), had a greater burden of atrial fibrillation but less diabetes. Higher bilirubin (T3 vs. T1) was associated with worse outcomes even after adjustment for other predictive variables, including NT‐proBNP and troponin T (adjusted hazard ratio for the primary outcome 1.73 [95% confidence interval 1.37–2.17], p < 0.001; and 1.52 [1.12–2.07], p = 0.01 for cardiovascular death). Baseline bilirubin did not modify the benefits of dapagliflozin. During follow‐up, dapagliflozin had no effect on liver tests. CONCLUSION: Bilirubin concentration was an independent predictor of worse outcomes but did not modify the benefits of dapagliflozin in HFrEF. Dapagliflozin was not associated with change in liver tests. Clinical Trial Registration: ClinicalTrials.gov NCT03036124.
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spelling pubmed-98051582023-01-06 Liver tests and outcomes in heart failure with reduced ejection fraction: findings from DAPA‐HF Adamson, Carly Cowan, Lorna M. de Boer, Rudolf A. Diez, Mirta Drożdż, Jarosław Dukát, Andre Inzucchi, Silvio E. Køber, Lars Kosiborod, Mikhail N. Ljungman, Charlotta E.A. Martinez, Felipe A. Ponikowski, Piotr Sabatine, Marc S. Lindholm, Daniel Bengtsson, Olof Boulton, David W. Greasley, Peter J. Langkilde, Anna Maria Sjöstrand, Mikaela Solomon, Scott D. McMurray, John J.V. Jhund, Pardeep S. Eur J Heart Fail Focused Issue on Clinical Trials AIMS: Reflecting both increased venous pressure and reduced cardiac output, abnormal liver tests are common in patients with severe heart failure and are associated with adverse clinical outcomes. We aimed to investigate the prognostic significance of abnormal liver tests in ambulatory patients with heart failure with reduced ejection fraction (HFrEF), explore any treatment interaction between bilirubin and sodium–glucose cotransporter 2 (SGLT2) inhibitors and examine change in liver tests with SGLT2 inhibitor treatment. METHODS AND RESULTS: We explored these objectives in the Dapagliflozin And Prevention of Adverse outcomes in Heart Failure (DAPA‐HF) trial, with focus on bilirubin. We calculated the incidence of cardiovascular death or worsening heart failure by bilirubin tertile. Secondary cardiovascular outcomes were examined, along with the change in liver tests at the end‐of‐study visit. Baseline bilirubin was available in 4720 patients (99.5%). Participants in the highest bilirubin tertile (T3) have more severe HFrEF (lower left ventricular ejection fraction, higher N‐terminal pro‐B‐type natriuretic peptide [NT‐proBNP] and worse New York Heart Association class), had a greater burden of atrial fibrillation but less diabetes. Higher bilirubin (T3 vs. T1) was associated with worse outcomes even after adjustment for other predictive variables, including NT‐proBNP and troponin T (adjusted hazard ratio for the primary outcome 1.73 [95% confidence interval 1.37–2.17], p < 0.001; and 1.52 [1.12–2.07], p = 0.01 for cardiovascular death). Baseline bilirubin did not modify the benefits of dapagliflozin. During follow‐up, dapagliflozin had no effect on liver tests. CONCLUSION: Bilirubin concentration was an independent predictor of worse outcomes but did not modify the benefits of dapagliflozin in HFrEF. Dapagliflozin was not associated with change in liver tests. Clinical Trial Registration: ClinicalTrials.gov NCT03036124. John Wiley & Sons, Ltd. 2022-08-22 2022-10 /pmc/articles/PMC9805158/ /pubmed/36054568 http://dx.doi.org/10.1002/ejhf.2649 Text en © 2022 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Focused Issue on Clinical Trials
Adamson, Carly
Cowan, Lorna M.
de Boer, Rudolf A.
Diez, Mirta
Drożdż, Jarosław
Dukát, Andre
Inzucchi, Silvio E.
Køber, Lars
Kosiborod, Mikhail N.
Ljungman, Charlotta E.A.
Martinez, Felipe A.
Ponikowski, Piotr
Sabatine, Marc S.
Lindholm, Daniel
Bengtsson, Olof
Boulton, David W.
Greasley, Peter J.
Langkilde, Anna Maria
Sjöstrand, Mikaela
Solomon, Scott D.
McMurray, John J.V.
Jhund, Pardeep S.
Liver tests and outcomes in heart failure with reduced ejection fraction: findings from DAPA‐HF
title Liver tests and outcomes in heart failure with reduced ejection fraction: findings from DAPA‐HF
title_full Liver tests and outcomes in heart failure with reduced ejection fraction: findings from DAPA‐HF
title_fullStr Liver tests and outcomes in heart failure with reduced ejection fraction: findings from DAPA‐HF
title_full_unstemmed Liver tests and outcomes in heart failure with reduced ejection fraction: findings from DAPA‐HF
title_short Liver tests and outcomes in heart failure with reduced ejection fraction: findings from DAPA‐HF
title_sort liver tests and outcomes in heart failure with reduced ejection fraction: findings from dapa‐hf
topic Focused Issue on Clinical Trials
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805158/
https://www.ncbi.nlm.nih.gov/pubmed/36054568
http://dx.doi.org/10.1002/ejhf.2649
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