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 inDiabetes care Vol. 44; no. 8; pp. 1894 - 1897
Main Authors Persson, Frederik, Rossing, Peter, Vart, Priya, Chertow, Glenn M., Hou, Fan Fan, Jongs, Niels, McMurray, John J.V., Correa-Rotter, Ricardo, Bajaj, Harpreet S., Stefansson, Bergur V., Toto, Robert D., Langkilde, Anna Maria, Wheeler, David C., Heerspink, Hiddo J.L.
Format Journal Article
LanguageEnglish
Published 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.
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.
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  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
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  surname: Vart
  fullname: Vart, Priya
  organization: Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands
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  givenname: Glenn M.
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  fullname: Chertow, Glenn M.
  organization: Departments of Medicine and Epidemiology and Population Health, Stanford University School of Medicine, Stanford, CA
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  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
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  givenname: Niels
  surname: Jongs
  fullname: Jongs, Niels
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  orcidid: 0000-0002-6317-3975
  surname: McMurray
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  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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2021 by the American Diabetes Association.
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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...
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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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