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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.
Cherney, David Z I; Cosentino, Francesco; McGuire, Darren K; Kolkailah, Ahmed A; Dagogo-Jack, Samuel; Pratley, Richard E; Frederich, Robert; Maldonado, Mario; Liu, Chih-Chin; Cannon, Christopher P.
Affiliation
  • Cherney DZI; Division of Nephrology, University Health Network, University of Toronto, Toronto, Ontario, Canada.
  • Cosentino F; Unit of Cardiology, Karolinska Institute and Karolinska University Hospital, Stockholm, Sweden.
  • McGuire DK; Division of Cardiology, University of Texas Southwestern Medical Center, and Parkland Health and Hospital System, Dallas, Texas, USA.
  • Kolkailah AA; Division of Cardiology, University of Texas Southwestern Medical Center, and Parkland Health and Hospital System, Dallas, Texas, USA.
  • Dagogo-Jack S; University of Tennessee Health Science Center, Memphis, Tennessee, USA.
  • Pratley RE; AdventHealth Translational Research Institute, Orlando, Florida, USA.
  • Frederich R; Pfizer Inc., Collegeville, Pennsylvania, USA.
  • Maldonado M; MSD Limited, London, UK.
  • Liu CC; Merck & Co., Inc., Rahway, New Jersey, USA.
  • Cannon CP; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Kidney Int Rep ; 8(4): 746-753, 2023 Apr.
Article in En | MEDLINE | ID: mdl-37069970
ABSTRACT

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 (111) to placebo, ertugliflozin 5 mg or 15 mg (doses pooled for analyses 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 m2 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. placebo 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 (P interaction  = 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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: Kidney Int Rep Year: 2023 Document type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: Kidney Int Rep Year: 2023 Document type: Article Affiliation country: Canada
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