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Novel Agents in the Management of Diabetes and the Risk of Worsening Diabetic Retinopathy
abstract
This abstract is available on the publisher's site.
Access this abstract nowPURPOSE
Novel therapies for diabetes have potent effects on glycemic control, obesity, and cardiovascular risk reduction, but some, including the popular drug semaglutide, have also been implicated in worsening of diabetic retinopathy (DR). Given the ubiquity of these new agents, understanding the risks to vision is important. Here, we review the data for several newly available agents in terms of systemic efficacy and retinal safety.
METHODS
Literature review.
RESULTS
Novel antihyperglycemic treatments include incretin mimetics and enhancers, sodium-glucose cotransporter inhibitors, long-acting insulins, and insulin delivery systems. All improve glycemic control, and some have been shown to reduce major cardiovascular outcomes. In a pivotal trial, semaglutide was associated with approximately 75% increased risk of DR worsening. The novel long-acting insulin icodec, formulated for once weekly dosing, showed increased risk of DR worsening over a once daily insulin. No other recent antihyperglycemic agent was associated with DR worsening, although following the semaglutide trials, nearly all studies excluded patients with preexisting DR. Cases of DR worsening were rare in all instances. Dedicated safety studies for semaglutide in DR are currently underway.
CONCLUSION
For most patients being considered for treatment with a novel antihyperglycemic agent, benefits on systemic metabolic and cardiovascular health are very likely to outweigh potential retinal harms. Although the true risks of the new agents on DR are unclear because their safety data come from secondary end points, the most vulnerable patients are those with preexisting high-risk DR, poor baseline glycemic control, and using insulin.
Additional Info
NOVEL AGENTS IN THE MANAGEMENT OF DIABETES AND RISK OF WORSENING DIABETIC RETINOPATHY
Retina (Philadelphia, Pa.) 2024 Nov 01;44(11)1851-1859, R Rajagopal, JB McGillFrom MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
Rajagopal and McGill published a comprehensive review to provide guidance on how to face the challenges associated with the use of novel glucose-lowering medicines for patients with diabetes in the real world. Specifically, the use of certain novel glucose-lowering drugs in clinical trials has been linked to an increased risk of worsening diabetic retinopathy (DR). For instance, the worsening of DR after using glucagon-like peptide 1 receptor agonists (GLP-1RAs) was documented in the SUSTAIN-6 trial. However, the current reviewers clearly pointed out that, in the SUSTAIN-6 trial, the safety data came from secondary endpoints, as the ocular outcomes were designed to be secondary in this study. Meanwhile, the most vulnerable patients, specifically those with preexisting high-risk DR, poor baseline glucose control, and using insulin, were recruited. Therefore, whether GLP-1RAs and their analogs are truly risky for DR worsening remains inconclusive.
Considering these caveats, the current review calls attention to additional clinical trials underway in which dedicated safety data should be primary DR endpoints. Overall, the documented benefits of GLP-1RAs and their analogs for glucose control and cardiovascular health likely outweigh their potential risks. Furthermore, the ocular benefits and potential risks of other novel glucose-lowering medicines, such as sodium-glucose co-transporter 2 inhibitors and various insulin agents, are also concisely discussed in this instructive review.