The impact of sodium‐glucose co‐transporter‐2 inhibitors on dementia and cardiovascular events in diabetic patients with atrial fibrillation

Author:

Chen Yun‐Yu123,Chang Hao‐Chih45,Lin Yenn‐Jiang24,Chien Kuo‐Liong6,Hsieh Yu‐Cheng17ORCID,Chung Fa‐Po24,Lin Ching‐Heng1,Lip Gregory Y. H.89,Chen Shih‐Ann147

Affiliation:

1. Department of Medical Research Taichung Veterans General Hospital Taichung Taiwan

2. Heart Rhythm Center Division of Cardiology Department of Medicine Taipei Veterans General Hospital Taipei Taiwan

3. Department of Post‐Baccalaureate Medicine and College of Life Sciences National Chung Hsing University Taichung Taiwan

4. Faculty of Medicine National Yang Ming Chiao Tung University Taipei Taiwan

5. Department of Medicine Taipei Veterans General Hospital Taoyuan Branch Taoyuan Taiwan

6. Institute of Epidemiology and Preventive Medicine College of Public Health National Taiwan University Taipei Taiwan

7. Cardiovascular Center Taichung Veterans General Hospital Taichung Taiwan

8. Liverpool Centre for Cardiovascular Science at University of Liverpool Liverpool John Moores University and Liverpool Heart & Chest Hospital Liverpool UK

9. Danish Center for Clinical Health Services Research Department of Clinical Medicine Aalborg University Aalborg Denmark

Abstract

AbstractAimsThe effectiveness of sodium‐glucose co‐transporter‐2 inhibitors (SGLT2i) on incident dementia in patients with diabetes and atrial fibrillation (AF) remains unknown. This study aimed to investigate the association between SGLT2i and the risk of incident dementia in diabetic patients with AF, and to explore the interactions with oral anticoagulants or dipeptidyl peptidase‐4 inhibitors (DPP4i).Materials and MethodsWe conducted a cohort study using Taiwan's National Health Insurance Research Database. Patients with diabetes and AFwithout a prior history of established cardiovascular diseases, were identified. Using propensity score matching, 810 patients receiving SGLT2i were matched with 1620 patients not receiving SGLT2i. The primary outcome was incident dementia, and secondary outcomes included composite cardiovascular events and mortality.ResultsAfter up to 5 years of follow‐up, SGLT2i use was associated with a significantly lower risk of incident dementia (hazard: 0.71, 95% confidence interval: 0.51–0.98), particularly vascular dementia (HR: 0.44, 95% CI: 0.24–0.82). SGLT2i was related to reduced risks of AF‐related hospitalisation (HR: 0.72, 95% CI: 0.56–0.93), stroke (HR: 0.75, 95% CI: 0.60–0.94), and all‐cause death (HR: 0.33, 95% CI: 0.24–0.44). The protective effects were consistent irrespective of the concurrent use of non‐vitamin K antagonist oral anticoagulants (NOACs) or DPP4i.ConclusionsIn diabetic patients with AF, SGLT2i was associated with reduced risks of incident dementia, AF‐related hospitalisation, stroke, and all‐cause death. The protective effects were independent of either concurrent use of NOACs or DPP4i.

Publisher

Wiley

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