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Sotagliflozin in patients with diabetes and chronic kidney disease

  • Deepak L. Bhatt*
  • , Michael Szarek
  • , Bertram Pitt
  • , Christopher P. Cannon
  • , Lawrence A. Leiter
  • , Darren K. McGuire
  • , Julia B. Lewis
  • , Matthew C. Riddle
  • , Silvio E. Inzucchi
  • , Mikhail N. Kosiborod
  • , David Z.I. Cherney
  • , Jamie P. Dwyer
  • , Benjamin M. Scirica
  • , Clifford J. Bailey
  • , Rafael Díaz
  • , Kausik K. Ray
  • , Jacob A. Udell
  • , Renato D. Lopes
  • , Pablo Lapuerta
  • , P. Gabriel Steg
  • *Corresponding author for this work
  • Harvard University
  • Colorado Prevention Center
  • State University of New York Downstate
  • University of Michigan
  • Li Ka Shing Knowledge Institute
  • University of Texas at Dallas
  • Vanderbilt University Medical Center
  • Oregon Health and Science University
  • Yale University
  • University of Missouri-Kansas City
  • University Health Network University of Toronto
  • Instituto Cardiovascular de Rosario
  • Royal Brompton Hospital
  • University Health Network
  • Duke Clinical Research Institute
  • Lexicon Pharmaceuticals
  • Institut National de la Santé et de la Recherche Médicale

Research output: Contribution to journalArticlepeer-review

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Abstract

BACKGROUND: The efficacy and safety of sodium-glucose cotransporter 2 inhibitors such as sotagliflozin in preventing cardiovascular events in patients with diabetes with chronic kidney disease with or without albuminuria have not been well studied.

METHODS: We conducted a multicenter, double-blind trial in which patients with type 2 diabetes mellitus (glycated hemoglobin level, ≥7%), chronic kidney disease (estimated glomerular filtration rate, 25 to 60 ml per minute per 1.73 m 2 of body-surface area), and risks for cardiovascular disease were randomly assigned in a 1:1 ratio to receive sotagliflozin or placebo. The primary end point was changed during the trial to the composite of the total number of deaths from cardiovascular causes, hospitalizations for heart failure, and urgent visits for heart failure. The trial ended early owing to loss of funding.

RESULTS: Of 19,188 patients screened, 10,584 were enrolled, with 5292 assigned to the sotagliflozin group and 5292 assigned to the placebo group, and followed for a median of 16 months. The rate of primary end-point events was 5.6 events per 100 patient-years in the sotagliflozin group and 7.5 events per 100 patient-years in the placebo group (hazard ratio, 0.74; 95% confidence interval [CI], 0.63 to 0.88; P<0.001). The rate of deaths from cardiovascular causes per 100 patient-years was 2.2 with sotagliflozin and 2.4 with placebo (hazard ratio, 0.90; 95% CI, 0.73 to 1.12; P = 0.35). For the original coprimary end point of the first occurrence of death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke, the hazard ratio was 0.84 (95% CI, 0.72 to 0.99); for the original coprimary end point of the first occurrence of death from cardiovascular causes or hospitalization for heart failure, the hazard ratio was 0.77 (95% CI, 0.66 to 0.91). Diarrhea, genital mycotic infections, volume depletion, and diabetic ketoacidosis were more common with sotagliflozin than with placebo.

CONCLUSIONS: In patients with diabetes and chronic kidney disease, with or without albuminuria, sotagliflozin resulted in a lower risk of the composite of deaths from cardiovascular causes, hospitalizations for heart failure, and urgent visits for heart failure than placebo but was associated with adverse events. (Funded by Sanofi and Lexicon Pharmaceuticals; SCORED ClinicalTrials.gov number, NCT03315143.).

Original languageEnglish
Pages (from-to)129-139
Number of pages11
JournalNew England Journal of Medicine
Volume384
Issue number2
Early online date16 Nov 2020
DOIs
Publication statusPublished - 14 Jan 2021

Bibliographical note

© 2020 Massachusetts Medical Society. All rights reserved.

Funding

Supported initially by Sanofi and then by Lexicon Pharmaceuticals. Dr. Ray received support from the National Institute for Health Research Imperial Biomedical Research Centre.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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