Efficacy and Safety of Dapagliflozin by Baseline Glycemic Status: A Prespecified Analysis From the DAPA-CKD Trial
OBJECTIVE The Dapagliflozin and Prevention of Adverse outcomes in Chronic Kidney Disease (DAPA-CKD) study demonstrated risk reduction for kidney and cardiovascular outcomes with dapagliflozin versus placebo in participants with chronic kidney disease (CKD) with and without diabetes. We compared outc...
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Published in | Diabetes care Vol. 44; no. 8; pp. 1894 - 1897 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Alexandria
American Diabetes Association
01.08.2021
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Abstract | OBJECTIVE The Dapagliflozin and Prevention of Adverse outcomes in Chronic Kidney Disease (DAPA-CKD) study demonstrated risk reduction for kidney and cardiovascular outcomes with dapagliflozin versus placebo in participants with chronic kidney disease (CKD) with and without diabetes. We compared outcomes according to baseline glycemic status. RESEARCH DESIGN AND METHODS We enrolled participants with CKD, estimated glomerular filtration rate (eGFR) 25–75 mL/min/1.73 m2, and urinary albumin-to-creatinine ratio 200–5,000 mg/g. The primary composite end point was sustained eGFR decline ≥50%, end-stage kidney disease, or kidney or cardiovascular death. RESULTS Of 4,304 participants, 738 had normoglycemia, 660 had prediabetes, and 2,906 had type 2 diabetes. The effect of dapagliflozin on the primary outcome was consistent (P for interaction = 0.19) in normoglycemia (hazard ratio [HR] 0.62 [95% CI 0.39, 1.01]), prediabetes (HR 0.37 [0.21, 0.66]), and type 2 diabetes (HR 0.64 [0.52, 0.79]). We found no evidence for effect modification on any outcome. Adverse events were similar, with no major hypoglycemia or ketoacidosis in participants with normoglycemia or prediabetes. CONCLUSIONS Dapagliflozin safely reduced kidney and cardiovascular events independent of baseline glycemic status. |
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AbstractList | The Dapagliflozin and Prevention of Adverse outcomes in Chronic Kidney Disease (DAPA-CKD) study demonstrated risk reduction for kidney and cardiovascular outcomes with dapagliflozin versus placebo in participants with chronic kidney disease (CKD) with and without diabetes. We compared outcomes according to baseline glycemic status.OBJECTIVEThe Dapagliflozin and Prevention of Adverse outcomes in Chronic Kidney Disease (DAPA-CKD) study demonstrated risk reduction for kidney and cardiovascular outcomes with dapagliflozin versus placebo in participants with chronic kidney disease (CKD) with and without diabetes. We compared outcomes according to baseline glycemic status.We enrolled participants with CKD, estimated glomerular filtration rate (eGFR) 25-75 mL/min/1.73 m2, and urinary albumin-to-creatinine ratio 200-5,000 mg/g. The primary composite end point was sustained eGFR decline ≥50%, end-stage kidney disease, or kidney or cardiovascular death.RESEARCH DESIGN AND METHODSWe enrolled participants with CKD, estimated glomerular filtration rate (eGFR) 25-75 mL/min/1.73 m2, and urinary albumin-to-creatinine ratio 200-5,000 mg/g. The primary composite end point was sustained eGFR decline ≥50%, end-stage kidney disease, or kidney or cardiovascular death.Of 4,304 participants, 738 had normoglycemia, 660 had prediabetes, and 2,906 had type 2 diabetes. The effect of dapagliflozin on the primary outcome was consistent (P for interaction = 0.19) in normoglycemia (hazard ratio [HR] 0.62 [95% CI 0.39, 1.01]), prediabetes (HR 0.37 [0.21, 0.66]), and type 2 diabetes (HR 0.64 [0.52, 0.79]). We found no evidence for effect modification on any outcome. Adverse events were similar, with no major hypoglycemia or ketoacidosis in participants with normoglycemia or prediabetes.RESULTSOf 4,304 participants, 738 had normoglycemia, 660 had prediabetes, and 2,906 had type 2 diabetes. The effect of dapagliflozin on the primary outcome was consistent (P for interaction = 0.19) in normoglycemia (hazard ratio [HR] 0.62 [95% CI 0.39, 1.01]), prediabetes (HR 0.37 [0.21, 0.66]), and type 2 diabetes (HR 0.64 [0.52, 0.79]). We found no evidence for effect modification on any outcome. Adverse events were similar, with no major hypoglycemia or ketoacidosis in participants with normoglycemia or prediabetes.Dapagliflozin safely reduced kidney and cardiovascular events independent of baseline glycemic status.CONCLUSIONSDapagliflozin safely reduced kidney and cardiovascular events independent of baseline glycemic status. OBJECTIVE The Dapagliflozin and Prevention of Adverse outcomes in Chronic Kidney Disease (DAPA-CKD) study demonstrated risk reduction for kidney and cardiovascular outcomes with dapagliflozin versus placebo in participants with chronic kidney disease (CKD) with and without diabetes. We compared outcomes according to baseline glycemic status. RESEARCH DESIGN AND METHODS We enrolled participants with CKD, estimated glomerular filtration rate (eGFR) 25–75 mL/min/1.73 m2, and urinary albumin-to-creatinine ratio 200–5,000 mg/g. The primary composite end point was sustained eGFR decline ≥50%, end-stage kidney disease, or kidney or cardiovascular death. RESULTS Of 4,304 participants, 738 had normoglycemia, 660 had prediabetes, and 2,906 had type 2 diabetes. The effect of dapagliflozin on the primary outcome was consistent (P for interaction = 0.19) in normoglycemia (hazard ratio [HR] 0.62 [95% CI 0.39, 1.01]), prediabetes (HR 0.37 [0.21, 0.66]), and type 2 diabetes (HR 0.64 [0.52, 0.79]). We found no evidence for effect modification on any outcome. Adverse events were similar, with no major hypoglycemia or ketoacidosis in participants with normoglycemia or prediabetes. CONCLUSIONS Dapagliflozin safely reduced kidney and cardiovascular events independent of baseline glycemic status. |
Author | Langkilde, Anna Maria Correa-Rotter, Ricardo Chertow, Glenn M. Jongs, Niels Bajaj, Harpreet S. Heerspink, Hiddo J.L. McMurray, John J.V. Stefansson, Bergur V. Toto, Robert D. Hou, Fan Fan Persson, Frederik Rossing, Peter Vart, Priya Wheeler, David C. |
Author_xml | – sequence: 1 givenname: Frederik orcidid: 0000-0001-6242-6638 surname: Persson fullname: Persson, Frederik organization: Steno Diabetes Center Copenhagen, Gentofte, Denmark – sequence: 2 givenname: Peter orcidid: 0000-0002-1531-4294 surname: Rossing fullname: Rossing, Peter organization: Steno Diabetes Center Copenhagen, Gentofte, Denmark, Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark – sequence: 3 givenname: Priya surname: Vart fullname: Vart, Priya organization: Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands – sequence: 4 givenname: Glenn M. surname: Chertow fullname: Chertow, Glenn M. organization: Departments of Medicine and Epidemiology and Population Health, Stanford University School of Medicine, Stanford, CA – sequence: 5 givenname: Fan Fan surname: Hou fullname: Hou, Fan Fan organization: Division of Nephrology, Nanfang Hospital, Southern Medical University, National Clinical Research Center for Kidney Disease, Guangzhou, China – sequence: 6 givenname: Niels surname: Jongs fullname: Jongs, Niels organization: Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands – sequence: 7 givenname: John J.V. orcidid: 0000-0002-6317-3975 surname: McMurray fullname: McMurray, John J.V. organization: Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, U.K – sequence: 8 givenname: Ricardo surname: Correa-Rotter fullname: Correa-Rotter, Ricardo organization: National Medical Science and Nutrition Institute Salvador Zubirán, Mexico City, Mexico – sequence: 9 givenname: Harpreet S. orcidid: 0000-0002-1461-1465 surname: Bajaj fullname: Bajaj, Harpreet S. organization: LMC Diabetes and Endocrinology, Brampton, Ontario, Canada – sequence: 10 givenname: Bergur V. surname: Stefansson fullname: Stefansson, Bergur V. organization: Late-stage Development, Cardiovascular, Renal and Metabolism, Biopharmaceuticals Research and Development, AstraZeneca, Gothenburg, Sweden – sequence: 11 givenname: Robert D. surname: Toto fullname: Toto, Robert D. organization: Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX – sequence: 12 givenname: Anna Maria surname: Langkilde fullname: Langkilde, Anna Maria organization: Late-stage Development, Cardiovascular, Renal and Metabolism, Biopharmaceuticals Research and Development, AstraZeneca, Gothenburg, Sweden – sequence: 13 givenname: David C. surname: Wheeler fullname: Wheeler, David C. organization: Department of Renal Medicine, University College London, London, U.K., The George Institute for Global Health, Sydney, Australia – sequence: 14 givenname: Hiddo J.L. orcidid: 0000-0002-3126-3730 surname: Heerspink fullname: Heerspink, Hiddo J.L. organization: Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands, The George Institute for Global Health, Sydney, Australia |
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Cites_doi | 10.3390/jcm8060779 10.1056/NEJMoa2024816 10.1007/s00125-020-05306-1 10.1053/j.ajkd.2020.04.016 10.1161/CIRCULATIONAHA.119.044359 10.1161/CIRCULATIONAHA.120.051824 10.1056/NEJMoa1911303 10.1016/j.kint.2020.04.051 |
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References | Anker (2022031309544248500_B4) 2021; 143 Li (2022031309544248500_B6) 2020; 98 Packer (2022031309544248500_B7) 2021; 77 Eickhoff (2022031309544248500_B8) 2019; 8 Heerspink (2022031309544248500_B1) 2020; 383 McMurray (2022031309544248500_B3) 2019; 381 Færch (2022031309544248500_B5) 2021; 64 Cannon (2022031309544248500_B2) 2020; 141 |
References_xml | – volume: 8 start-page: 779 year: 2019 ident: 2022031309544248500_B8 article-title: Effects of dapagliflozin on volume status when added to renin-angiotensin system inhibitors publication-title: J Clin Med doi: 10.3390/jcm8060779 – volume: 383 start-page: 1436 year: 2020 ident: 2022031309544248500_B1 article-title: Dapagliflozin in patients with chronic kidney disease publication-title: N Engl J Med doi: 10.1056/NEJMoa2024816 – volume: 64 start-page: 42 year: 2021 ident: 2022031309544248500_B5 article-title: The effects of dapagliflozin, metformin or exercise on glycaemic variability in overweight or obese individuals with prediabetes (the PRE-D Trial): a multi-arm, randomised, controlled trial publication-title: Diabetologia doi: 10.1007/s00125-020-05306-1 – volume: 77 start-page: 280 year: 2021 ident: 2022031309544248500_B7 article-title: Mechanisms leading to differential hypoxia-inducible factor signaling in the diabetic kidney: modulation by SGLT2 inhibitors and hypoxia mimetics publication-title: Am J Kidney Dis doi: 10.1053/j.ajkd.2020.04.016 – volume: 141 start-page: 407 year: 2020 ident: 2022031309544248500_B2 article-title: Evaluating the effects of canagliflozin on cardiovascular and renal events in patients with type 2 diabetes mellitus and chronic kidney disease according to baseline HbA1c, Including those with HbA1c <7%: results from the CREDENCE Trial publication-title: Circulation doi: 10.1161/CIRCULATIONAHA.119.044359 – volume: 143 start-page: 337 year: 2021 ident: 2022031309544248500_B4 article-title: Effect of empagliflozin on cardiovascular and renal outcomes in patients with heart failure by baseline diabetes status: results from the EMPEROR-Reduced Trial publication-title: Circulation doi: 10.1161/CIRCULATIONAHA.120.051824 – volume: 381 start-page: 1995 year: 2019 ident: 2022031309544248500_B3 article-title: Dapagliflozin in patients with heart failure and reduced ejection fraction publication-title: N Engl J Med doi: 10.1056/NEJMoa1911303 – volume: 98 start-page: 769 year: 2020 ident: 2022031309544248500_B6 article-title: Mediators of the effects of canagliflozin on kidney protection in patients with type 2 diabetes publication-title: Kidney Int doi: 10.1016/j.kint.2020.04.051 |
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Snippet | OBJECTIVE The Dapagliflozin and Prevention of Adverse outcomes in Chronic Kidney Disease (DAPA-CKD) study demonstrated risk reduction for kidney and... The Dapagliflozin and Prevention of Adverse outcomes in Chronic Kidney Disease (DAPA-CKD) study demonstrated risk reduction for kidney and cardiovascular... |
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SubjectTerms | Albumins Antidiabetics Creatinine Diabetes Diabetes mellitus Diabetes mellitus (non-insulin dependent) Diabetic ketoacidosis End-stage renal disease Epidermal growth factor receptors Glomerular filtration rate Glucose Health risks Hypoglycemia Ketoacidosis Kidney diseases Kidneys Novel Communications in Diabetes Research design Risk management |
Title | Efficacy and Safety of Dapagliflozin by Baseline Glycemic Status: A Prespecified Analysis From the DAPA-CKD Trial |
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