Early Change in Albuminuria with Canagliflozin Predicts Kidney and Cardiovascular Outcomes: A


Journal

Journal of the American Society of Nephrology : JASN
ISSN: 1533-3450
Titre abrégé: J Am Soc Nephrol
Pays: United States
ID NLM: 9013836

Informations de publication

Date de publication:
12 2020
Historique:
received: 24 05 2020
accepted: 11 08 2020
pubmed: 2 10 2020
medline: 13 3 2021
entrez: 1 10 2020
Statut: ppublish

Résumé

The association between early changes in albuminuria and kidney and cardiovascular events is primarily based on trials of renin-angiotensin system blockade. It is unclear whether this association occurs with sodium-glucose cotransporter 2 inhibition. The Canagliflozin and Renal Events in Diabetes with Established Nephropathy Clinical Evaluation (CREDENCE) trial enrolled 4401 patients with type 2 diabetes and CKD (urinary albumin-creatinine ratio [UACR] >300 mg/g). This Complete data for early change in albuminuria and other covariates were available for 3836 (87.2%) participants in the CREDENCE trial. Compared with placebo, canagliflozin lowered UACR by 31% (95% confidence interval [95% CI], 27% to 36%) at week 26, and significantly increased the likelihood of achieving a 30% reduction in UACR (odds ratio, 2.69; 95% CI, 2.35 to 3.07). Each 30% decrease in UACR over the first 26 weeks was independently associated with a lower hazard for the primary kidney outcome (hazard ratio [HR], 0.71; 95% CI, 0.67 to 0.76; In people with type 2 diabetes and CKD, use of canagliflozin results in early, sustained reductions in albuminuria, which were independently associated with long-term kidney and cardiovascular outcomes.

Sections du résumé

BACKGROUND
The association between early changes in albuminuria and kidney and cardiovascular events is primarily based on trials of renin-angiotensin system blockade. It is unclear whether this association occurs with sodium-glucose cotransporter 2 inhibition.
METHODS
The Canagliflozin and Renal Events in Diabetes with Established Nephropathy Clinical Evaluation (CREDENCE) trial enrolled 4401 patients with type 2 diabetes and CKD (urinary albumin-creatinine ratio [UACR] >300 mg/g). This
RESULTS
Complete data for early change in albuminuria and other covariates were available for 3836 (87.2%) participants in the CREDENCE trial. Compared with placebo, canagliflozin lowered UACR by 31% (95% confidence interval [95% CI], 27% to 36%) at week 26, and significantly increased the likelihood of achieving a 30% reduction in UACR (odds ratio, 2.69; 95% CI, 2.35 to 3.07). Each 30% decrease in UACR over the first 26 weeks was independently associated with a lower hazard for the primary kidney outcome (hazard ratio [HR], 0.71; 95% CI, 0.67 to 0.76;
CONCLUSIONS
In people with type 2 diabetes and CKD, use of canagliflozin results in early, sustained reductions in albuminuria, which were independently associated with long-term kidney and cardiovascular outcomes.

Identifiants

pubmed: 32998938
pii: ASN.2020050723
doi: 10.1681/ASN.2020050723
pmc: PMC7790219
doi:

Substances chimiques

Sodium-Glucose Transporter 2 Inhibitors 0
Canagliflozin 0SAC974Z85

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2925-2936

Informations de copyright

Copyright © 2020 by the American Society of Nephrology.

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Auteurs

Megumi Oshima (M)

The George Institute for Global Health, University of New South Wales Sydney, Sydney, Australia.
Department of Nephrology and Laboratory Medicine, Kanazawa University, Kanazawa, Japan.

Brendon L Neuen (BL)

The George Institute for Global Health, University of New South Wales Sydney, Sydney, Australia.

JingWei Li (J)

The George Institute for Global Health, University of New South Wales Sydney, Sydney, Australia h.j.lambers.heerspink@umcg.nl.

Vlado Perkovic (V)

The George Institute for Global Health, University of New South Wales Sydney, Sydney, Australia.

David M Charytan (DM)

Nephrology Division, School of Medicine and Langone Medical Center, New York University, New York, New York.
Baim Institute for Clinical Research, Boston, Massachusetts.

Dick de Zeeuw (D)

Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Robert Edwards (R)

Janssen Research & Development, LLC, Raritan, New Jersey.

Tom Greene (T)

Division of Biostatistics, Department of Population Health Sciences, University of Utah, Salt Lake City, Utah.

Adeera Levin (A)

Division of Nephrology, University of British Columbia, Vancouver, Canada.

Kenneth W Mahaffey (KW)

Stanford Center for Clinical Research, Department of Medicine, Stanford University School of Medicine, Stanford, California.

Luca De Nicola (L)

Department of Advanced Medical and Surgical Sciences, Nephrology and Dialysis Unit, University Vanvitelli, Naples, Italy.

Carol Pollock (C)

Kolling Institute of Medical Research, Sydney Medical School, University of Sydney, Royal North Shore Hospital, St Leonards, Australia.

Norman Rosenthal (N)

Janssen Research & Development, LLC, Raritan, New Jersey.

David C Wheeler (DC)

The George Institute for Global Health, University of New South Wales Sydney, Sydney, Australia.
Department of Renal Medicine, University College London Medical School, London, United Kingdom.

Meg J Jardine (MJ)

The George Institute for Global Health, University of New South Wales Sydney, Sydney, Australia.
Concord Repatriation General Hospital, Sydney, Australia.

Hiddo J L Heerspink (HJL)

The George Institute for Global Health, University of New South Wales Sydney, Sydney, Australia h.j.lambers.heerspink@umcg.nl.
Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

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Classifications MeSH