Cherney David Z I, Dagogo-Jack Samuel, Cosentino Francesco, Pratley Richard E, Frederich Robert, Maldonado Mario, Liu Chih-Chin, Cannon Christopher P
Division of Nephrology, University of Toronto, Toronto, Ontario, Canada.
Division of Endocrinology, Diabetes & Metabolism & Director, Clinical Research Center, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Kidney Int Rep. 2022 May 13;7(8):1782-1792. doi: 10.1016/j.ekir.2022.05.007. eCollection 2022 Aug.
Using data from the VERTIS CV trial (NCT01986881), the impact of ertugliflozin in patients with nonalbuminuric diabetic kidney disease (DKD-non-Alb) was assessed.
Patients with type 2 diabetes mellitus (T2DM) and atherosclerotic cardiovascular disease (ASCVD) were randomized to ertugliflozin or placebo. Subgroups were defined by estimated glomerular filtration rate (eGFR) (ml/min per 1.73 m) and urinary albumin-to-creatinine ratios (UACRs) (mg/g): DKD-Non-Alb (eGFR < 60 + UACR < 30, 867); Alb DKD stage 3 (DKD stage 3 Alb, eGFR < 60 + UACR ≥ 30, 891); Alb DKD stages 1 + 2 (DKD stages 1-2 Alb, eGFR ≥ 60 + UACR ≥ 30, 2356); and no DKD (non-DKD, eGFR ≥ 60 + UACR < 30, 3916). eGFR slopes, eGFR and UACR over time, time to first event of a prespecified exploratory kidney composite outcome, albuminuria progression, and hospitalization for heart failure (HHF) were assessed.
Total eGFR slopes (ml/min per 1.73 m per year; weeks 0-260) with placebo were -0.23, -1.27, -2.29, and -1.19 for the DKD-Non-Alb, DKD stage 3 Alb, DKD stages 1 to 2 Alb, and non-DKD subgroups, respectively ( < 0.0001). Similar trends were found with ertugliflozin but with reduced rates of decline. Ertugliflozin treatment resulted in a significant reduction in the risk for albuminuria progression across subgroups, with Alb subgroups having the largest relative risk reduction ( = 0.04). The hazard ratios (HRs) for ertugliflozin revealing reduction in the risk of the exploratory kidney composite outcome versus placebo was consistent across subgroups ( = 0.34). Alb and the DKD-non-Alb subgroups had a larger relative risk reduction in the HHF outcome compared with other subgroups ( = 0.046).
Among the subgroups, participants with DKD-non-Alb had the slowest rate of eGFR decline. Ertugliflozin treatment resulted in reductions in albuminuria and slower decline in eGFR across subgroups. The effect of ertugliflozin on the HHF outcome was larger in those with more advanced kidney disease.
利用VERTIS CV试验(NCT01986881)的数据,评估了依鲁格列净对非白蛋白尿性糖尿病肾病(DKD-非Alb)患者的影响。
将2型糖尿病(T2DM)和动脉粥样硬化性心血管疾病(ASCVD)患者随机分为依鲁格列净组或安慰剂组。根据估计肾小球滤过率(eGFR)(ml/min per 1.73 m)和尿白蛋白与肌酐比值(UACR)(mg/g)定义亚组:DKD-非Alb(eGFR < 60 + UACR < 30,867例);白蛋白尿性DKD 3期(DKD 3期Alb,eGFR < 60 + UACR≥30,891例);白蛋白尿性DKD 1 + 2期(DKD 1-2期Alb,eGFR≥60 + UACR≥30,2356例);以及无DKD(非DKD,eGFR≥60 + UACR < 30,3916例)。评估了eGFR斜率、随时间变化的eGFR和UACR、达到预先指定的探索性肾脏复合结局的首次事件时间、蛋白尿进展情况以及因心力衰竭住院(HHF)情况。
安慰剂组DKD-非Alb、DKD 3期Alb、DKD 1至2期Alb和非DKD亚组的总eGFR斜率(ml/min per 1.73 m每年;第0至260周)分别为-0.23、-1.27、-2.29和-1.19(P < 0.0001)。依鲁格列净组也发现了类似趋势,但下降速率降低。依鲁格列净治疗导致各亚组蛋白尿进展风险显著降低,白蛋白尿亚组的相对风险降低幅度最大(P = 0.04)。依鲁格列净与安慰剂相比,降低探索性肾脏复合结局风险的风险比(HRs)在各亚组中一致(P = 0.34)。与其他亚组相比,白蛋白尿亚组和DKD-非Alb亚组在HHF结局方面的相对风险降低幅度更大(P = 0.046)。
在各亚组中,DKD-非Alb参与者的eGFR下降速率最慢。依鲁格列净治疗导致各亚组蛋白尿减少且eGFR下降减缓。依鲁格列净对HHF结局的影响在肾病更严重的患者中更大。