Cited by 16Retinal Diseases and TreatmentsDiabetes Treatment and ManagementDrug-Induced Ocular Toxicity

Glucagon-like Peptide-1 receptor agonists are not associated with an increased risk of progressing to vision-threatening diabetic retinopathy

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Tauqeer, Zujaja, Bracha, Peter, Hua, Peiying, Yu, Yinxi, Cui, Qi N., VanderBeek, Brian L.·2025·Ophthalmic Epidemiology

Abstract

Purpose Glucagon-like peptide-1 receptor agonists (GLP-1RA) are used to treat type 2 diabetes mellitus (DM) by augmenting insulin release and sensitivity. We assessed the overall risk for development of vision-threatening diabetic retinopathy (VTDR), proliferative diabetic retinopathy (PDR), and diabetic macular edema (DME), among GLP-1RA users.Methods A retrospective cohort of patients with NPDR newly started on a GLP-1RA from a national insurance claims database was compared to a cohort of patients treated with other oral anti-diabetic agents and matched for age, sex, race, index year, and number of active diabetic medications. Exclusions occurred for < 2 years in the database before diagnosis; prior diagnoses of PDR, DME, vitreous hemorrhage, and/or other retinal vascular diseases; and prior intraocular treatment for VTDR.Results A total of 6093 users of GLP-1RA were matched to 14,122 controls. In the GLP-1RA cohort, 632 (10.1%), 76 (1.2%), and 544 (8.9%) patients progressed to VTDR, PDR, or DME, respectively. This is compared to 1332 (9.5%) VTDR, 165 (1.2%) PDR, or 1148 (8.1%) DME in the control group. Accounting for underlying DM severity with IPTW, no difference in hazard was seen in the GLP-1RA cohort compared to controls for progression to VTDR (HR = 1.02, 95%CI: 0.92–1.14 p = 0.69), DME (HR = 1.06, 95%CI: 0.95–1.1.9, p = 0.31), or PDR (HR = 0.81, 95%CI: 0.58–1.12, p = 0.20).Conclusion We found no difference in the risk for vision-threatening diabetic retinopathy, nor for its component diseases, DME or PDR, with GLP-1RA use compared to other oral anti-hyperglycemic agents in patients with NPDR.

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Crossref · 10.1080/09286586.2024.2399764

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Authors
Tauqeer, Z., Bracha, P., Hua, P., Yu, Y., Cui, Q. N., & VanderBeek, B. L.
Affiliations
  • Associated Retinal Consultants (US)
  • Wolfe Eye Clinic (US)
  • University of Pennsylvania (US)
Corresponding author
VanderBeek, Brian L.
Venue
Ophthalmic Epidemiology
Published
2024-10-10
Volume
32
Issue
4
Pages
390-393
ISSN
  • 0928-6586 (ISSN-L)
  • 1744-5086
OpenAlex
W4403289459
Cited by
16
References
12
Citations by year
2026: 8 · 2025: 8
FWCI
6.36
Type
journal article
Language
en
Open access
Locations
  • Ophthalmic Epidemiology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Eye Institute (K23EY025729, P30EY001583, R01EY034115)
Topics
  • Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Health Sciences › Medicine › Ophthalmology › Drug-Induced Ocular Toxicity
Keywords
GLP-1 receptor agonists, diabetic retinopathy, proliferative diabetic retinopathy, diabetic macular edema, non-proliferative diabetic retinopathy, type 2 diabetes, drug safety, retinal disease progression
MeSH terms
Glucagon-Like Peptide-1 Receptor Agonists, Adult, Aged, Diabetes Mellitus, Type 2, Diabetic Retinopathy, Female, Humans, Hypoglycemic Agents, Macular Edema, Male, Middle Aged, Retrospective Studies, Risk Factors, Disease Progression

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