Effects of Ertugliflozin on Kidney Outcomes in Patients With Heart Failure at Baseline in the Evaluation of Ertugliflozin Efficacy and Safety Cardiovascular Outcomes (VERTIS CV) Trial

被引:1
|
作者
Cherney, David Z. I. [1 ,12 ]
Cosentino, Francesco [2 ,3 ]
McGuire, Darren K. [4 ,5 ]
Kolkailah, Ahmed A. [4 ,5 ]
Dagogo-Jack, Samuel [6 ]
Pratley, Richard E. [7 ]
Frederich, Robert [8 ]
Maldonado, Mario [9 ]
Liu, Chih-Chin [10 ]
Cannon, Christopher P. [11 ]
机构
[1] Univ Toronto, Univ Hlth Network, Div Nephrol, Toronto, ON, Canada
[2] Karolinska Inst, Unit Cardiol, Stockholm, Sweden
[3] Karolinska Univ Hosp, Stockholm, Sweden
[4] Univ Texas Southwestern Med Ctr, Div Cardiol, Dallas, TX USA
[5] Parkland Hlth & Hosp Syst, Dallas, TX USA
[6] Univ Tennessee, Hlth Sci Ctr, Memphis, TN USA
[7] AdventHlth Translat Res Inst, Orlando, FL USA
[8] Pfizer Inc, Collegeville, PA USA
[9] MSD Ltd, London, England
[10] Merck & Co Inc, Rahway, NJ USA
[11] Harvard Med Sch, Brigham & Womens Hosp, Cardiovasc Div, Boston, MA USA
[12] Univ Toronto, Univ Hlth Network, Toronto Gen Hosp, Div Nephrol, 585 Univ Ave,8N-845, Toronto, ON M5G 2N2, Canada
来源
KIDNEY INTERNATIONAL REPORTS | 2023年 / 8卷 / 04期
基金
美国国家卫生研究院;
关键词
albuminuria; diabetic kidney disease; ertugliflozin; heart failure; sodium-glucose cotransporter 2 inhibi-tor; type 2 diabetes mellitus; EMPAGLIFLOZIN; DISEASE; RISK;
D O I
10.1016/j.ekir.2023.01.011
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
Introduction: In the eValuation of ERTugliflozin effIcacy and Safety CardioVascular outcomes (VERTIS CV) trial (NCT01986881), patients with type 2 diabetes mellitus (T2DM) and atherosclerotic cardiovascular disease (ASCVD) were randomized (1:1:1) to placebo, ertugliflozin 5 mg or 15 mg (doses pooled for an-alyses as prospectively planned). In this post hoc analysis, the effects of ertugliflozin on kidney outcomes were assessed in analyses stratified by baseline heart failure (HF).Methods: Baseline HF was defined as a history of HF or prerandomization left ventricular ejection fraction =45%. Outcomes included estimated glomerular filtration rate (eGFR) over time, total 5-year eGFR slopes and time to first event of a prespecified exploratory kidney composite outcome of sustained $40% decrease from baseline eGFR, chronic kidney replacement therapy, or kidney death. All analyses were stratified by baseline HF status.Results: Compared with no-HF at baseline (n = 5807; 70.4%), patients with HF (n = 2439; 29.6%) had a notably faster rate of eGFR decline, which is unlikely to be explained by the slightly lower baseline eGFR in that group. Ertugliflozin treatment resulted in a slower rate of eGFR decline in both subgroups; total placebo-adjusted 5-year eGFR slopes (ml/min per 1.73 m(2) per year [95% confidence intervals; CI]) were 0.96 (0.67-1.24) and 0.95 (0.76-1.14) for HF and no-HF subgroups, respectively. The placebo HF (vs. pla-cebo no-HF) subgroup had a higher incidence of the composite kidney outcome (35/834 [4.20%] vs. 50/ 1913 [2.61%]). Hazard ratios (95% CI) for the effect of ertugliflozin on the composite kidney outcome did not differ significantly between HF and no-HF subgroups: 0.53 (0.33-0.84) and 0.76 (0.53-1.08), respectively (Pinteraction = 0.22).Conclusion: Although patients with HF at baseline had a faster rate of eGFR decline in VERTIS CV, the beneficial effects of ertugliflozin on kidney outcomes did not differ when stratified by baseline HF.Kidney Int Rep (2023) 8, 746-753; https://doi.org/10.1016/j.ekir.2023.01.011
引用
收藏
页码:746 / 753
页数:8
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