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Association between uric acid levels and cardio‐renal outcomes and death in patients with type 2 diabetes: A subanalysis of EMPA‐REG OUTCOME

In the EMPA‐REG OUTCOME trial, we explored the association between pre‐randomization uric acid level tertile (<309.30 μmol/L; 309.30 to <387.21 μmol/L; ≥387.21 μmol/L) and cardiovascular (CV) death, hospitalization for heart failure (HHF), HHF or CV death, all‐cause mortality, three‐point majo...

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Autores principales: Verma, Subodh, Ji, Qiuhe, Bhatt, Deepak L., Mazer, C. David, Al‐Omran, Mohammed, Inzucchi, Silvio E., Wanner, Christoph, Ofstad, Anne Pernille, Zwiener, Isabella, George, Jyothis T., Zinman, Bernard, Fitchett, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317186/
https://www.ncbi.nlm.nih.gov/pubmed/32030863
http://dx.doi.org/10.1111/dom.13991
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author Verma, Subodh
Ji, Qiuhe
Bhatt, Deepak L.
Mazer, C. David
Al‐Omran, Mohammed
Inzucchi, Silvio E.
Wanner, Christoph
Ofstad, Anne Pernille
Zwiener, Isabella
George, Jyothis T.
Zinman, Bernard
Fitchett, David
author_facet Verma, Subodh
Ji, Qiuhe
Bhatt, Deepak L.
Mazer, C. David
Al‐Omran, Mohammed
Inzucchi, Silvio E.
Wanner, Christoph
Ofstad, Anne Pernille
Zwiener, Isabella
George, Jyothis T.
Zinman, Bernard
Fitchett, David
author_sort Verma, Subodh
collection PubMed
description In the EMPA‐REG OUTCOME trial, we explored the association between pre‐randomization uric acid level tertile (<309.30 μmol/L; 309.30 to <387.21 μmol/L; ≥387.21 μmol/L) and cardiovascular (CV) death, hospitalization for heart failure (HHF), HHF or CV death, all‐cause mortality, three‐point major adverse CV events (MACE), and incident or worsening nephropathy. Patients with type 2 diabetes and CV disease received empagliflozin or placebo. The median baseline plasma uric acid level was 344.98 μmol/L, and patients’ baseline characteristics were mainly balanced across tertiles. Baseline uric acid levels were associated with cardio‐renal outcomes: in the placebo group, for the highest versus lowest tertile, the multivariable hazard ratios for three‐point MACE, HHF or CV death, and incident or worsening nephropathy were 1.22 (95% confidence interval [CI] 0.89–1.67; P = 0.2088), 1.51 (95% CI 1.02–2.23; P = 0.0396) and 1.77 (95% CI 1.33–2.34; P < 0.0001), respectively. When tested as a continuous variable, baseline uric acid was associated with all outcomes in the placebo group. Empagliflozin improved all cardio‐renal outcomes across tertiles, with all interaction P values >0.05. Further investigation of these relationships is required.
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spelling pubmed-73171862020-06-30 Association between uric acid levels and cardio‐renal outcomes and death in patients with type 2 diabetes: A subanalysis of EMPA‐REG OUTCOME Verma, Subodh Ji, Qiuhe Bhatt, Deepak L. Mazer, C. David Al‐Omran, Mohammed Inzucchi, Silvio E. Wanner, Christoph Ofstad, Anne Pernille Zwiener, Isabella George, Jyothis T. Zinman, Bernard Fitchett, David Diabetes Obes Metab Brief Reports In the EMPA‐REG OUTCOME trial, we explored the association between pre‐randomization uric acid level tertile (<309.30 μmol/L; 309.30 to <387.21 μmol/L; ≥387.21 μmol/L) and cardiovascular (CV) death, hospitalization for heart failure (HHF), HHF or CV death, all‐cause mortality, three‐point major adverse CV events (MACE), and incident or worsening nephropathy. Patients with type 2 diabetes and CV disease received empagliflozin or placebo. The median baseline plasma uric acid level was 344.98 μmol/L, and patients’ baseline characteristics were mainly balanced across tertiles. Baseline uric acid levels were associated with cardio‐renal outcomes: in the placebo group, for the highest versus lowest tertile, the multivariable hazard ratios for three‐point MACE, HHF or CV death, and incident or worsening nephropathy were 1.22 (95% confidence interval [CI] 0.89–1.67; P = 0.2088), 1.51 (95% CI 1.02–2.23; P = 0.0396) and 1.77 (95% CI 1.33–2.34; P < 0.0001), respectively. When tested as a continuous variable, baseline uric acid was associated with all outcomes in the placebo group. Empagliflozin improved all cardio‐renal outcomes across tertiles, with all interaction P values >0.05. Further investigation of these relationships is required. Blackwell Publishing Ltd 2020-03-28 2020-07 /pmc/articles/PMC7317186/ /pubmed/32030863 http://dx.doi.org/10.1111/dom.13991 Text en © 2020 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://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 Brief Reports
Verma, Subodh
Ji, Qiuhe
Bhatt, Deepak L.
Mazer, C. David
Al‐Omran, Mohammed
Inzucchi, Silvio E.
Wanner, Christoph
Ofstad, Anne Pernille
Zwiener, Isabella
George, Jyothis T.
Zinman, Bernard
Fitchett, David
Association between uric acid levels and cardio‐renal outcomes and death in patients with type 2 diabetes: A subanalysis of EMPA‐REG OUTCOME
title Association between uric acid levels and cardio‐renal outcomes and death in patients with type 2 diabetes: A subanalysis of EMPA‐REG OUTCOME
title_full Association between uric acid levels and cardio‐renal outcomes and death in patients with type 2 diabetes: A subanalysis of EMPA‐REG OUTCOME
title_fullStr Association between uric acid levels and cardio‐renal outcomes and death in patients with type 2 diabetes: A subanalysis of EMPA‐REG OUTCOME
title_full_unstemmed Association between uric acid levels and cardio‐renal outcomes and death in patients with type 2 diabetes: A subanalysis of EMPA‐REG OUTCOME
title_short Association between uric acid levels and cardio‐renal outcomes and death in patients with type 2 diabetes: A subanalysis of EMPA‐REG OUTCOME
title_sort association between uric acid levels and cardio‐renal outcomes and death in patients with type 2 diabetes: a subanalysis of empa‐reg outcome
topic Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317186/
https://www.ncbi.nlm.nih.gov/pubmed/32030863
http://dx.doi.org/10.1111/dom.13991
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