Primary and Secondary Cardiovascular and Kidney Prevention With Canagliflozin: Insights From the CANVAS Program and CREDENCE Trial

Author:

Sharma Abhinav123ORCID,Razaghizad Amir123ORCID,Joury Abdulaziz1234,Levin Adeera5ORCID,Bajaj Harpreet S.6ORCID,Mancini G. B. John7ORCID,Wong Norman C.8,Slee April9ORCID,Ang Fernando G.10ORCID,Rapattoni Wally10ORCID,Neuen Brendon L.1112ORCID,Arnott Clare11131415ORCID,Perkovic Vlado111213ORCID,Mahaffey Kenneth W.16ORCID

Affiliation:

1. Centre for Outcomes Research and Evaluation Research Institute of the McGill University Health Centre Montreal QC Canada

2. Division of Cardiology McGill University Health Centre, McGill University Montreal QC Canada

3. DREAM‐CV Laboratory McGill University Health Centre, McGill University Montreal QC Canada

4. King Salman Heart Center, King Fahad Medical City Riyadh Saudi Arabia

5. Division of Nephrology University of British Columbia Vancouver BC Canada

6. LMC Healthcare Brampton ON Canada

7. Centre for Cardiovascular Innovation University of British Columbia Vancouver BC Canada

8. University of Calgary AB Canada

9. New Arch Consulting Seattle WA

10. Janssen, Inc. Toronto ON Canada

11. The George Institute for Global Health, UNSW Sydney Sydney Australia

12. Royal North Shore Hospital Sydney Australia

13. Faculty of Medicine, UNSW Sydney Sydney Australia

14. Department of Cardiology Royal Prince Alfred Hospital Sydney Australia

15. Sydney Medical School University of Sydney Australia

16. Stanford Center for Clinical Research, Department of Medicine Stanford University School of Medicine Stanford CA

Abstract

Background This study evaluated the effects of canagliflozin in patients with type 2 diabetes with and without prevalent cardiovascular disease (secondary and primary prevention). Methods and Results This was a pooled participant‐level analysis of the CANVAS (Canagliflozin Cardiovascular Assessment Study) Program and CREDENCE (Canagliflozin and Renal Events in Diabetes With Established Nephropathy Clinical Evaluation) trial. The CANVAS Program included participants with type 2 diabetes at elevated cardiovascular risk, whereas the CREDENCE trial included participants with type 2 diabetes and albuminuric chronic kidney disease. Hazard ratios (HRs) with interaction terms were obtained from Cox regression models to estimate relative risk reduction with canagliflozin versus placebo across the primary and secondary prevention groups. We analyzed 5616 (38.9%) and 8804 (61.1%) individuals in the primary and secondary prevention subgroups, respectively. Primary versus secondary prevention participants were on average younger (62.2 versus 63.8 years of age) and more often women (42% versus 31%). Canagliflozin reduced the risk of major adverse cardiovascular events (HR, 0.84 [95% CI, 0.76–0.94]) consistently across primary and secondary prevention subgroups ( P interaction =0.86). Similarly, no treatment effect heterogeneity was observed with canagliflozin for hospitalization for heart failure, cardiovascular death, end‐stage kidney disease, or all‐cause mortality (all P interaction >0.5). Conclusions Canagliflozin reduced cardiovascular and kidney outcomes with no statistical evidence of heterogeneity for the treatment effect across the primary and secondary prevention subgroups in the CANVAS Program and CREDENCE trial. Although studies on the optimal implementation of canagliflozin within these populations are warranted, these results reinforce canagliflozin's role in cardiorenal prevention and treatment in individuals with type 2 diabetes. Registration URL: https://www.clinicaltrials.gov ; Unique identifiers: NCT01032629, NCT01989754, NCT02065791.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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