Risk of Diabetic Retinopathy in Patients With Type 2 Diabetes After SGLT‐2 Inhibitors: A Nationwide Population Cohort Study

Author:

Huang Shih‐Ting123,Bair Pei‐Jane34,Chang Shih‐Sheng35,Kao Yu‐Nong13,Chen San‐Ni6,Wang I‐Kang34,Chiu Chih‐Wei1,Chang Chi‐Tzung3,Shih Ying‐Hsiu7,Li Chi‐Yuan4,Yu Tung‐Min134ORCID

Affiliation:

1. Division of Nephrology Taichung Veterans General Hospital Taichung Taiwan

2. Department of Post‐Baccalaureate Medicine, College of Medicine National Chung Hsing University Taichung Taiwan

3. School of Medicine China Medical University Taichung Taiwan

4. Graduate Institute of Biomedical Sciences, School of Medicine, China Medical University Taichung Taiwan

5. Division of Cardiovascular Medicine China Medical University Hospital Taichung Taiwan

6. Department of Ophthalmology China Medical University Hospital Taichung Taiwan

7. Management Office for Health Data China Medical University Hospital Taichung Taiwan

Abstract

Diabetic retinopathy (DR) accounts for 80% of cases of vision loss in patients with type 2 diabetes mellitus (T2DM). Interventional treatments are only indicated in advanced DR and are ineffective in some patients. Sodium–glucose cotransporter 2 inhibitors (SGLT2is) are used to attenuate T2DM‐associated cardiovascular complications. We conducted the cohort study to investigate the effect of SGLT2is on DR development. Data (May 2016–December 2018) obtained from the Taiwan National Health Insurance Research Database were analyzed in this nationwide retrospective cohort study. After propensity score matching, a total of 31,764 patients receiving SGLT2is and another 31,764 patients receiving dipeptidyl peptidase 4 inhibitors (DPP4is) were included in this study. Multiple Cox proportional‐hazards regression models were used to evaluate DR risk. Overall DR incidence among SGLT2i or DPP4i users was 10.9 or 15.6 per 10,000 patient‐years, respectively. After covariate adjustment, DR (both early and late stage) risk was substantially lower in SGLT2i users (adjusted hazard ratio: 0.68, 95% confidence interval: 0.6–0.78) than in DPP4i users. DR risk appears to be considerably lower in SGLT2i users than in DPP4i users. Glycemic control measurement with HbA1C level was unavailable in this claim database.

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

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