Safety of sodium‐glucose co‐transporter‐2 inhibitors on amputation across categories of baseline cardiovascular disease and diuretics use in patients with type 2 diabetes

Author:

Park Sohee12,Jeong Han Eol13,Bea Sungho1,Yu Oriana H. Y.45,Cho Young Min6789ORCID,You Seng Chan10,Man Kenneth K. C.21112,Shin Ju‐Young1313ORCID

Affiliation:

1. School of Pharmacy Sungkyunkwan University Suwon Republic of Korea

2. Research Department of Practice and Policy UCL School of Pharmacy London UK

3. Department of Biohealth Regulatory Science Sungkyunkwan University Suwon Republic of Korea

4. Centre for Clinical Epidemiology Lady Davis Institute, Jewish General Hospital Montreal Quebec Canada

5. Division of Endocrinology and Metabolism Jewish General Hospital, McGill University Montreal Quebec Canada

6. Department of Internal Medicine Seoul National University College of Medicine Seoul South Korea

7. Department of Translational Medicine Seoul National University College of Medicine Seoul South Korea

8. Department of Internal Medicine Seoul National University Hospital Seoul South Korea

9. Institute on Aging Seoul National University Seoul South Korea

10. Department of Biomedical Systems Informatics Yonsei University College of Medicine Seoul Republic of Korea

11. Centre for Medicines Optimisation Research and Education University College London Hospitals NHS Foundation Trust London UK

12. Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy LKS Faculty of Medicine, University of Hong Kong Hong Kong Hong Kong

13. Department of Clinical Research Design & Evaluation, Samsung Advanced Institute for Health Sciences & Technology Sungkyunkwan University Seoul Republic of Korea

Abstract

AbstractAimTo assess the risk of amputation associated with sodium‐glucose co‐transporter‐2 inhibitors (SGLT2is) among patients with type 2 diabetes, across categories of baseline cardiovascular disease (CVD) and diuretic use (DU).Materials and MethodsWe conducted an active comparator, new‐user cohort study using Korea's nationwide claims data (2015‐2020). The study cohort consisted of patients with type 2 diabetes who initiated SGLT2is or dipeptidyl peptidase‐4 inhibitors (DPP4is). Cohort entry was defined by first prescription date. We then classified patients into four discrete subcohorts based on their baseline status of CVD and DU as (1) CVD+/DU+, (2) CVD+/DU‐, (3) CVD‐/DU+ and (4) CVD‐/DU‐. We performed 1:1 propensity score (PS) matching within each cohort and estimated hazard ratios (HRs) with 95% confidence intervals (CIs) for the risk of amputation with SGLT2is versus DPP4is using Cox models.ResultsWe identified 219 900 PS‐matched pairs of SGLT2is and DPP4is (CVD+/DU+, n = 11 719; CVD+/DU‐, n = 26 092; CVD‐/DU+, n = 26 894; and CVD‐/DU‐, n = 155 195), with well‐balanced baseline covariates across all cohorts. Significantly lower risks of amputation with SGLT2is versus DPP4is were found in CVD+/DU+ (HR 0.36, 95% CI 0.14‐0.90), CVD+/DU‐ (0.45, 0.21‐0.99) and CVD‐/DU‐ (0.48, 0.33‐0.70), but not in CVD‐/DU+ (0.54, 0.26‐1.12). Consistent trends in estimates were found across various sensitivity analyses.ConclusionsInitiating SGLT2is against DPP4is did not increase the risk of amputation across patient populations of varying vulnerability. These findings based on routine practice will reassure clinicians of the safety of SGLT2is with regard to amputation risk in selected high‐risk patients with type 2 diabetes.

Funder

Ministry of Food and Drug Safety

National Research Foundation of Korea

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

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