Type 2 & other diabetes

Geographic and racial variability in kidney, cardiovascular and safety outcomes with canagliflozin: A secondary analysis of the CREDENCE randomized trial

Diabetes Obes MetabPublished Secondary analysis of the CREDENCE randomised trial

Authors' conclusion

Canagliflozin reduces the risk of kidney and cardiovascular events similarly across geographic regions and racial groups.

Study context

Population
Individuals with T2D and CKD, across six geographic regions (North America 1182, Central and South America 941, Eastern Europe 947, Western Europe 421, Asia 749, Other 161) and four racial groups (White 2931, Black or African American 224, Asian 877, Other 369)
Participants
4,401 individuals
Comparison
Canagliflozin vs placebo
Primary endpoint
Composite of:
  • End-stage kidney disease (ESKD)
  • Doubling of serum creatinine (SCr)
  • Death from kidney or cardiovascular causes
Methodological detailssubgroup analysis by geographic region and racial group, stratified Cox proportional hazards model
  • Subgroup analysis by geographic region and racial group
  • Stratified Cox proportional hazards model

Primary result

As reported in the abstract

Canagliflozin consistently reduced the primary composite endpoint across geographic regions without evidence of heterogeneity
interaction P=0.39
Canagliflozin consistently reduced the primary composite endpoint across racial groups without evidence of heterogeneity
interaction P=0.91

Secondary outcomes

Primary composite outcome, overall trial

HR (95% CI)P value
CanagliflozinRelative risk reduced by 30%0.70 (0.59–0.82)P = 0.00001

Safety

No significant safety outcome differences across geographic regions and racial groups

Original publication

Geographic and racial variability in kidney, cardiovascular and safety outcomes with canagliflozin: A secondary analysis of the CREDENCE randomized trial. Diabetes Obes Metab. Published 19 June 2024. doi:10.1111/dom.15685

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

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