Association of type III collagen turnover with cardiovascular outcomes and impact with canagliflozin in the CANVAS Program: A post hoc analysis.

Yunyun Luo, Daniel G K Rasmussen, Federica Genovese, Peder Frederiksen, Michael K Hansen, Morten A Karsdal, Bruce Neal, Martin Pehrsson

Journal: Diabetes, obesity & metabolism 2024;26(9):4060-4068

PMID: 39014523

Abstract

AIM

To investigate type III collagen (COL III) turnover in participants from the CANVAS Program biomarker substudy.

METHODS

Biomarkers of COL III formation (PRO-C3) and COL III degradation fragments (C3M and CTX-III) were assessed in baseline and year 3 plasma from patients enrolled in CANVAS, investigating the effect of canagliflozin in participants with type 2 diabetes. The clinical outcomes investigated in this study were hospitalization for heart failure, cardiovascular death and all-cause mortality.

RESULTS

Higher levels of PRO-C3 and C3M at baseline were associated with an increased incidence of all investigated outcomes, whereas levels of CTX-III at baseline were not associated with any of the investigated outcomes. Levels of PRO-C3 decreased and levels of CTX-III increased following canagliflozin treatment. An increase from baseline to year 3 in PRO-C3 in the placebo arm was associated with an increased incidence of cardiovascular outcomes, and in all participants was associated with an increased risk of all-cause mortality.

CONCLUSIONS

The changes in PRO-C3 and CTX-III reflect a shift in the dynamics of COL3 turnover following treatment with canagliflozin. These biomarkers are promising pharmacodynamic tools that can be used to monitor the impact of canagliflozin treatment and possibly other sodium-glucose co-transporter-2 inhibitors on tissue remodelling in future interventional trials.

© 2024 John Wiley & Sons Ltd.

Address: Nordic Bioscience, Herlev, Denmark.; Janssen Research & Development, LLC, Spring House, Pennsylvania, USA.; The George Institute for Global Health, UNSW Sydney, Sydney, New South Wales, Australia.; The Charles Perkins Centre, University of Sydney, Sydney, New South Wales, Australia.; Imperial College London, London, UK.
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