Type 2 & other diabetes

Estimated lifetime benefit of novel pharmacological therapies in patients with type 2 diabetes and chronic kidney disease: A joint analysis of randomized controlled clinical trials

Diabetes Obes MetabPublished Joint analysis of randomised controlled trials

Primary result · Primary composite outcomeResult — go to the resultHazard ratio 0.50 95% CI 0.44–0.57

Authors' conclusion

Combined disease-modifying treatment with an SGLT2 inhibitor and MRA in patients with type 2 diabetes and CKD may substantially increase the number of years free from kidney failure and mortality.

Study context

Population
Patients with T2D and chronic kidney disease (CKD); effect estimates from CREDENCE and FIDELIO, applied to DAPA-CKD control group with T2DCREDENCE 4,401 · FIDELIO 5,734
Comparison
SGLT2i + mineralocorticoid-receptor antagonists (MRA) combination vs ACE inhibitors/angiotensin receptor blockers
Primary endpoint
Composite of:
  • Doubling of serum creatinine
  • End-stage kidney disease
  • Death because of kidney failure
Methodological detailstrial-level estimates from CREDENCE and FIDELIO applied to DAPA-CKD control group, repeated in an observational study
  • Trial-level estimates from CREDENCE and FIDELIO applied to DAPA-CKD control group
  • Repeated in an observational study

Primary result

Primary composite outcome

Hazard ratio

0.50

95% CI 0.44–0.57

Combination treatmentvs ACE inhibitors/ARBs
HR 0.50 (95% CI 0.44–0.57)

As reported in the abstract

Further findings

OutcomeCombination treatmentIncremental gain (years) (95% CI)
Estimated event-free survival from primary outcome · at age 50 yearsCombination treatment vs ACE inhibitors/ARBs16.7 (CI 18.1–21.0) years6.7 (5.5–7.9)
  • Estimated event-free survival from primary outcome: ACE inhibitors/ARBs 10.0 (CI 6.8–12.3) years

Gain in event-free survival from primary outcome, observational study

Estimated gain in event-free survival
6.3 years (95% CI: 5.2, 7.3)

Gain in event-free survival from primary outcome, conservative scenario

Gain in event-free survival
2.5 years (95% CI: 2.0, 2.9)
  • Low adherence (70% of the observed adherence) and less pronounced efficacy (70% of the observed efficacy with 2% yearly decline)

Original publication

Estimated lifetime benefit of novel pharmacological therapies in patients with type 2 diabetes and chronic kidney disease: A joint analysis of randomized controlled clinical trials. Diabetes Obes Metab. Published 14 August 2023. doi:10.1111/dom.15232

Composed by AI from the published abstract and checked against it. How Briefs are made →

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