The evaluation of noninferiority for renal composite outcomes between sodium-glucose cotransporter inhibitors in Japan

Prim Care Diabetes. 2021 Dec;15(6):1058-1062. doi: 10.1016/j.pcd.2021.08.012. Epub 2021 Sep 4.

Abstract

Background: In Japan, six types of sodium-glucose cotransporter inhibitors (SGLT2Is) are currently in use. Here, we evaluated differences in renal composite outcomes between SGLT2Is with or without evidence of cardio vascular outcome trials (CVOTs).

Methods: We retrospectively surveyed 536 Japanese patients with type 2 diabetes mellitus with chronic kidney disease who received SGLT2Is for more than 1 year. Patients were classified as having received empagliflozin, canagliflozin, or dapagliflozin (n = 270, Evidence (+) group) or as having received ipragliflozin, tofogliflozin, or luseogliflozin (n = 266, Evidence (-) group). The propensity score matching method was performed.

Result: On matched cohort model including 205 cases in each group, there were no significant differences in the incidence of renal composite outcomes (n = 28 [14%] in the Evidence (+) group, n = 21 [10%] in the Evidence (-) group for the matched model; p = 0.29) between groups. Cox hazard analyses in the matched cohort model showed that the risk ratio for renal composite outcomes in the Evidence (-) group was 0.73 (95% confidence interval: 0.40-1.32), which was greater than the noninferiority margin of 1.22.

Conclusion: Three SGLT2Is with no CVOT's evidence did not show noninferiority compared with other SGLT2Is with evidences.

Keywords: Diabetic nephropathy; Non-inferiority; Renal composite outcome; SGLT2 inhibitor.

MeSH terms

  • Diabetes Mellitus, Type 2* / diagnosis
  • Diabetes Mellitus, Type 2* / drug therapy
  • Diabetes Mellitus, Type 2* / epidemiology
  • Glucose
  • Humans
  • Hypoglycemic Agents / adverse effects
  • Japan / epidemiology
  • Retrospective Studies
  • Sodium
  • Sodium-Glucose Transporter 2 Inhibitors* / adverse effects

Substances

  • Hypoglycemic Agents
  • Sodium-Glucose Transporter 2 Inhibitors
  • Sodium
  • Glucose