What is the risk to vision for non-diabetic individuals taking GLP-1 (Glucagon-Like Peptide-1) receptor agonists?

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Last updated: November 5, 2025View editorial policy

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Vision Risk for Non-Diabetic Patients Taking GLP-1 Receptor Agonists

For non-diabetic individuals taking GLP-1 receptor agonists, the primary vision concern is an increased risk of nonarteritic anterior ischemic optic neuropathy (NAION), particularly with semaglutide, while diabetic retinopathy is not a concern in this population.

Key Vision Risks in Non-Diabetic Patients

NAION Risk with Semaglutide

  • Semaglutide carries a significantly elevated risk of NAION in non-diabetic patients using it for weight loss, with a hazard ratio of 7.64 (95% CI, 2.21-26.36) compared to non-GLP-1 RA weight-loss medications 1.

  • The cumulative incidence of NAION over 36 months was 6.7% in patients prescribed semaglutide versus 0.8% in those on non-GLP-1 RA weight-loss medications 1.

  • This translates to approximately 1 in 15 non-diabetic patients on semaglutide developing NAION over 3 years, compared to 1 in 125 on alternative weight-loss medications 1.

Diabetic Retinopathy Considerations

  • Diabetic retinopathy is not a concern for non-diabetic patients taking GLP-1 receptor agonists, as this complication requires pre-existing diabetes and chronic hyperglycemia 2.

  • The retinopathy concerns documented with GLP-1 RAs apply specifically to diabetic patients with existing retinopathy who experience rapid A1C reductions 2.

Clinical Management Algorithm

Pre-Treatment Assessment

  • Obtain baseline ophthalmologic evaluation focusing on optic nerve health and risk factors for NAION before initiating GLP-1 RA therapy in non-diabetic patients 1.

  • Document specific NAION risk factors including: history of optic neuropathy, small optic disc with crowded appearance ("disc at risk"), obstructive sleep apnea, hypertension, and nocturnal hypotension 1.

During Treatment Monitoring

  • Counsel patients to immediately report any sudden vision loss, particularly monocular vision changes upon awakening, as NAION typically presents with sudden, painless vision loss 1.

  • Consider more frequent ophthalmologic monitoring (every 6-12 months) for patients with multiple NAION risk factors while on semaglutide 3.

Risk-Benefit Considerations

  • The number needed to harm for NAION with semaglutide in non-diabetic patients is approximately 17 over 36 months 1.

  • For patients with cardiovascular disease, the cardiovascular benefits may outweigh vision risks, as semaglutide reduces cardiovascular events with a hazard ratio of 0.80 (95% CI, 0.72-0.90) 2.

Alternative GLP-1 RA Options

  • Consider liraglutide as an alternative if NAION risk is particularly concerning, as the association with NAION appears strongest with semaglutide 1.

  • Tirzepatide (dual GIP/GLP-1 agonist) achieved superior weight loss (20.9% at 72 weeks) in non-diabetic patients, though NAION data are limited 2.

Common Pitfalls to Avoid

  • Do not dismiss sudden vision changes as benign, as NAION can cause permanent vision loss and requires immediate ophthalmologic evaluation 1.

  • Do not confuse diabetic retinopathy risks (relevant only to diabetic patients) with NAION risks (relevant to all patients on semaglutide) 2, 1.

  • Do not assume all GLP-1 RAs carry equal NAION risk, as current evidence specifically implicates semaglutide 1.

Additional Protective Effects

  • GLP-1 RAs may provide protective effects against glaucoma, age-related macular degeneration, and dry eye disease through anti-inflammatory mechanisms 3.

  • These potential benefits should be weighed against NAION risk when making treatment decisions 3.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Glucagon-like peptide-1 receptor agonists and the eye.

Current opinion in ophthalmology, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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