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Dapagliflozin reduces uric acid concentration, an independent predictor of adverse outcomes in DAPA‐HF

AIMS: Blood uric acid (UA) levels are frequently elevated in patients with heart failure and reduced ejection fraction (HFrEF), may lead to gout and are associated with worse outcomes. Reduction in UA is desirable in HFrEF and sodium–glucose cotransporter 2 inhibitors may have this effect. We aimed...

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Autores principales: McDowell, Kirsty, Welsh, Paul, Docherty, Kieran F., Morrow, David A., Jhund, Pardeep S., de Boer, Rudolf A., O'Meara, Eileen, Inzucchi, Silvio E., Køber, Lars, Kosiborod, Mikhail N., Martinez, Felipe A., Ponikowski, Piotr, Hammarstedt, Ann, Langkilde, Anna Maria, Sjöstrand, Mikaela, Lindholm, Daniel, Solomon, Scott D., Sattar, Naveed, Sabatine, Marc S., McMurray, John J.V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540869/
https://www.ncbi.nlm.nih.gov/pubmed/35064721
http://dx.doi.org/10.1002/ejhf.2433
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author McDowell, Kirsty
Welsh, Paul
Docherty, Kieran F.
Morrow, David A.
Jhund, Pardeep S.
de Boer, Rudolf A.
O'Meara, Eileen
Inzucchi, Silvio E.
Køber, Lars
Kosiborod, Mikhail N.
Martinez, Felipe A.
Ponikowski, Piotr
Hammarstedt, Ann
Langkilde, Anna Maria
Sjöstrand, Mikaela
Lindholm, Daniel
Solomon, Scott D.
Sattar, Naveed
Sabatine, Marc S.
McMurray, John J.V.
author_facet McDowell, Kirsty
Welsh, Paul
Docherty, Kieran F.
Morrow, David A.
Jhund, Pardeep S.
de Boer, Rudolf A.
O'Meara, Eileen
Inzucchi, Silvio E.
Køber, Lars
Kosiborod, Mikhail N.
Martinez, Felipe A.
Ponikowski, Piotr
Hammarstedt, Ann
Langkilde, Anna Maria
Sjöstrand, Mikaela
Lindholm, Daniel
Solomon, Scott D.
Sattar, Naveed
Sabatine, Marc S.
McMurray, John J.V.
author_sort McDowell, Kirsty
collection PubMed
description AIMS: Blood uric acid (UA) levels are frequently elevated in patients with heart failure and reduced ejection fraction (HFrEF), may lead to gout and are associated with worse outcomes. Reduction in UA is desirable in HFrEF and sodium–glucose cotransporter 2 inhibitors may have this effect. We aimed to examine the association between UA and outcomes, the effect of dapagliflozin according to baseline UA level, and the effect of dapagliflozin on UA in patients with HFrEF in the DAPA‐HF trial. METHODS AND RESULTS: The association between UA and the primary composite outcome of cardiovascular death or worsening heart failure, its components, and all‐cause mortality was examined using Cox regression analyses among 3119 patients using tertiles of UA, after adjustment for other prognostic variables. Change in UA from baseline over 12 months was also evaluated. Patients in tertile 3 (UA ≥6.8 mg/dl) versus tertile 1 (<5.4 mg/dl) were younger (66.3 ± 10.8 vs. 68 ± 10.2 years), more often male (83.1% vs. 71.5%), had lower estimated glomerular filtration rate (58.2 ± 17.4 vs. 70.6 ± 18.7 ml/min/1.73 m(2)), and more often treated with diuretics. Higher UA was associated with a greater risk of the primary outcome (adjusted hazard ratio tertile 3 vs. tertile 1: 1.32, 95% confidence interval [CI] 1.06–1.66; p = 0.01). The risk of heart failure hospitalization and cardiovascular death increased by 7% and 6%, respectively per 1 mg/dl unit increase of UA (p = 0.04 and p = 0.07). Spline analysis revealed a linear increase in risk above a cut‐off UA value of 7.09 mg/dl. Compared with placebo, dapagliflozin reduced UA by 0.84 mg/dl (95% CI −0.93 to −0.74) over 12 months (p < 0.001). Dapagliflozin improved outcomes, irrespective of baseline UA concentration. CONCLUSION: Uric acid remains an independent predictor of worse outcomes in a well‐treated contemporary HFrEF population. Compared with placebo, dapagliflozin reduced UA and improved outcomes irrespective of UA concentration.
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spelling pubmed-95408692022-10-14 Dapagliflozin reduces uric acid concentration, an independent predictor of adverse outcomes in DAPA‐HF McDowell, Kirsty Welsh, Paul Docherty, Kieran F. Morrow, David A. Jhund, Pardeep S. de Boer, Rudolf A. O'Meara, Eileen Inzucchi, Silvio E. Køber, Lars Kosiborod, Mikhail N. Martinez, Felipe A. Ponikowski, Piotr Hammarstedt, Ann Langkilde, Anna Maria Sjöstrand, Mikaela Lindholm, Daniel Solomon, Scott D. Sattar, Naveed Sabatine, Marc S. McMurray, John J.V. Eur J Heart Fail TREATMENT OF HFrEF AIMS: Blood uric acid (UA) levels are frequently elevated in patients with heart failure and reduced ejection fraction (HFrEF), may lead to gout and are associated with worse outcomes. Reduction in UA is desirable in HFrEF and sodium–glucose cotransporter 2 inhibitors may have this effect. We aimed to examine the association between UA and outcomes, the effect of dapagliflozin according to baseline UA level, and the effect of dapagliflozin on UA in patients with HFrEF in the DAPA‐HF trial. METHODS AND RESULTS: The association between UA and the primary composite outcome of cardiovascular death or worsening heart failure, its components, and all‐cause mortality was examined using Cox regression analyses among 3119 patients using tertiles of UA, after adjustment for other prognostic variables. Change in UA from baseline over 12 months was also evaluated. Patients in tertile 3 (UA ≥6.8 mg/dl) versus tertile 1 (<5.4 mg/dl) were younger (66.3 ± 10.8 vs. 68 ± 10.2 years), more often male (83.1% vs. 71.5%), had lower estimated glomerular filtration rate (58.2 ± 17.4 vs. 70.6 ± 18.7 ml/min/1.73 m(2)), and more often treated with diuretics. Higher UA was associated with a greater risk of the primary outcome (adjusted hazard ratio tertile 3 vs. tertile 1: 1.32, 95% confidence interval [CI] 1.06–1.66; p = 0.01). The risk of heart failure hospitalization and cardiovascular death increased by 7% and 6%, respectively per 1 mg/dl unit increase of UA (p = 0.04 and p = 0.07). Spline analysis revealed a linear increase in risk above a cut‐off UA value of 7.09 mg/dl. Compared with placebo, dapagliflozin reduced UA by 0.84 mg/dl (95% CI −0.93 to −0.74) over 12 months (p < 0.001). Dapagliflozin improved outcomes, irrespective of baseline UA concentration. CONCLUSION: Uric acid remains an independent predictor of worse outcomes in a well‐treated contemporary HFrEF population. Compared with placebo, dapagliflozin reduced UA and improved outcomes irrespective of UA concentration. John Wiley & Sons, Ltd. 2022-02-06 2022-06 /pmc/articles/PMC9540869/ /pubmed/35064721 http://dx.doi.org/10.1002/ejhf.2433 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-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle TREATMENT OF HFrEF
McDowell, Kirsty
Welsh, Paul
Docherty, Kieran F.
Morrow, David A.
Jhund, Pardeep S.
de Boer, Rudolf A.
O'Meara, Eileen
Inzucchi, Silvio E.
Køber, Lars
Kosiborod, Mikhail N.
Martinez, Felipe A.
Ponikowski, Piotr
Hammarstedt, Ann
Langkilde, Anna Maria
Sjöstrand, Mikaela
Lindholm, Daniel
Solomon, Scott D.
Sattar, Naveed
Sabatine, Marc S.
McMurray, John J.V.
Dapagliflozin reduces uric acid concentration, an independent predictor of adverse outcomes in DAPA‐HF
title Dapagliflozin reduces uric acid concentration, an independent predictor of adverse outcomes in DAPA‐HF
title_full Dapagliflozin reduces uric acid concentration, an independent predictor of adverse outcomes in DAPA‐HF
title_fullStr Dapagliflozin reduces uric acid concentration, an independent predictor of adverse outcomes in DAPA‐HF
title_full_unstemmed Dapagliflozin reduces uric acid concentration, an independent predictor of adverse outcomes in DAPA‐HF
title_short Dapagliflozin reduces uric acid concentration, an independent predictor of adverse outcomes in DAPA‐HF
title_sort dapagliflozin reduces uric acid concentration, an independent predictor of adverse outcomes in dapa‐hf
topic TREATMENT OF HFrEF
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540869/
https://www.ncbi.nlm.nih.gov/pubmed/35064721
http://dx.doi.org/10.1002/ejhf.2433
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