Effect of Canagliflozin on Renal and Cardiovascular Outcomes across Different Levels of Albuminuria: Data from the CANVAS Program

被引:104
作者
Neuen, Brendon L. [1 ]
Ohkuma, Toshiaki [1 ]
Neal, Bruce [1 ]
Matthews, David R. [2 ]
de Zeeuw, Dick [3 ]
Mahaffey, Kenneth W. [4 ]
Fulcher, Greg [5 ]
Li, Qiang [1 ]
Jardine, Meg [1 ]
Oh, Richard [6 ]
Heerspink, Hiddo L. [1 ,3 ]
Perkovic, Vlado [1 ]
机构
[1] Univ New South Wales, George Inst Global Hlth, Sydney, NSW, Australia
[2] Univ Oxford, Harris Manchester Coll, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England
[3] Univ Groningen, Univ Med Ctr Groningen, Groningen, Netherlands
[4] Stanford Univ, Dept Med, Stanford Ctr Clin Res, Sch Med, Stanford, CA 94305 USA
[5] Royal North Shore Hosp, Sydney, NSW, Australia
[6] Janssen Res & Dev LLC, Raritan, NJ USA
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2019年 / 30卷 / 11期
关键词
SGLT2; inhibitor; canagliflozin; renal; cardiovascular; albuminuria; GLOMERULAR-FILTRATION-RATE; TYPE-2; DIABETES-MELLITUS; CHRONIC KIDNEY-DISEASE; COLLABORATIVE METAANALYSIS; EMPAGLIFLOZIN; RISK; MICROALBUMINURIA; INSUFFICIENCY; INHIBITION; MORTALITY;
D O I
10.1681/ASN.2019010064
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background If SGLT2 inhibitors protect the kidneys by reducing albuminuria as hypothesized, people with type 2 diabetes mellitus (T2DM) with higher albuminuria should benefit more. Methods We conducted a post-hoc analysis of data from the CANagliflozin cardioVascular Assessment Study (CANVAS) Program, which randomized 10,142 participants with T2DM and high cardiovascular risk to canagliflozin or placebo. We assessed effects of canagliflozin on renal, cardiovascular, and safety outcomes by baseline albuminuria. The trial included 2266 participants (22.3%) with moderately increased albuminuria (urinary albumin/creatinine ratio [UACR] 30-300 mg/g) and 760 (7.5%) with severely increased albuminuria (UACR >300 mg/g) at baseline. Results Canagliflozin lowered albuminuria with greater proportional reductions in those with moderately and severely increased albuminuria (P heterogeneity<0.001). After week 13, canagliflozin slowed the annual loss of kidney function across albuminuria subgroups, with greater absolute reductions in participants with severely increased albuminuria (placebo-subtracted difference 3.01 ml/min per 1.73 m(2) per year; P heterogeneity<0.001). Heterogeneity for the renal composite outcome of 40% reduction in eGFR, ESKD, or renal-related death was driven by lesser effects in participants with moderately increased albuminuria (P heterogeneity=0.03), but no effect modification was observed when albuminuria was fitted as a continuous variable (P heterogeneity=0.94). Cardiovascular and safety outcomes were mostly consistent across albuminuria levels including increased risks for amputation across albuminuria subgroups (P heterogeneity=0.66). Greater absolute risk reductions in the renal composite outcome were observed in participants with severely increased albuminuria (P heterogeneity=0.004). Conclusions The proportional effects of canagliflozin on renal and cardiovascular outcomes are mostly consistent across patients with different levels of albuminuria, but absolute benefits are greatest among those with severely increased albuminuria.
引用
收藏
页码:2229 / 2242
页数:14
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