Back to Search Start Over

Effects of Dapagliflozin in Stage 4 Chronic Kidney Disease.

Authors :
Chertow GM
Vart P
Jongs N
Toto RD
Gorriz JL
Hou FF
McMurray JJV
Correa-Rotter R
Rossing P
Sjöström CD
Stefánsson BV
Langkilde AM
Wheeler DC
Heerspink HJL
Source :
Journal of the American Society of Nephrology : JASN [J Am Soc Nephrol] 2021 Sep; Vol. 32 (9), pp. 2352-2361. Date of Electronic Publication: 2021 Jul 16.
Publication Year :
2021

Abstract

Background: In the Dapagliflozin and Prevention of Adverse Outcomes in Chronic Kidney Disease (DAPA-CKD) randomized, placebo-controlled trial, the sodium-glucose cotransporter 2 inhibitor dapagliflozin significantly reduced risk of kidney failure and prolonged survival in patients with CKD with or without type 2 diabetes.<br />Methods: Adults with eGFR of 25-75 ml/min per 1.73 m <superscript>2</superscript> and urinary albumin-to-creatinine ratio of 200-5000 mg/g had been randomized to receive dapagliflozin 10 mg/d or placebo. Here, we conducted a prespecified analysis of dapagliflozin's effects in patients with stage 4 CKD (eGFR,30 ml/min per 1.73 m <superscript>2</superscript> ) at baseline. The primary end point was a composite of time to ≥50% sustained decline in eGFR, ESKD, or kidney or cardiovascular death. Secondary end points were a kidney composite (same as the primary end point but without cardiovascular death), a composite of cardiovascular death or heart failure hospitalization, and all-cause death.<br />Results: A total of 293 participants with stage 4 CKD received dapagliflozin and 331 received placebo. Patients with stage 4 CKD randomized to dapagliflozin experienced a 27% (95% confidence interval [95% CI]: -2 to 47%) reduction in the primary composite endpoint, and 29% (-2 to 51%), 17% (-53 to 55%), and 32% (-21 to 61%) reductions in the kidney, cardiovascular and mortality endpoints, respectively, relative to placebo. Interaction P-values were 0.22, 0.13, 0.63, and 0.95, respectively, comparing CKD stages 4 versus 2/3. The eGFR slope declined by 2.15 and 3.38 ml/min per 1.73 m <superscript>2</superscript> per year in the dapagliflozin and placebo groups, respectively ( P =0.005). Patients treated with dapagliflozin or placebo had similar rates of serious adverse events and adverse events of interest.<br />Conclusions: Among patients with stage 4 CKD and albuminuria, the effects of dapagliflozin were consistent with those observed in the DAPA-CKD trial overall, with no evidence of increased risks.<br /> (Copyright © 2021 by the American Society of Nephrology.)

Details

Language :
English
ISSN :
1533-3450
Volume :
32
Issue :
9
Database :
MEDLINE
Journal :
Journal of the American Society of Nephrology : JASN
Publication Type :
Academic Journal
Accession number :
34272327
Full Text :
https://doi.org/10.1681/ASN.2021020167