Department of Ophthalmology and Visual Sciences, and.
Division of Endocrinology, Metabolism, and Lipid Research, Washington University School of Medicine, Saint Louis, Missouri.
Retina. 2024 Nov 1;44(11):1851-1859. doi: 10.1097/IAE.0000000000004252.
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.
Literature review.
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.
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.
新型糖尿病疗法在血糖控制、肥胖和心血管风险降低方面具有显著效果,但其中一些药物,包括广受欢迎的司美格鲁肽,也被认为会加重糖尿病视网膜病变(DR)。鉴于这些新药物的广泛应用,了解其对视力的影响非常重要。在此,我们根据几项新的可用药物的系统疗效和视网膜安全性来评估其数据。
文献回顾。
新型抗高血糖治疗药物包括肠促胰岛素类似物和增效剂、钠-葡萄糖共转运蛋白抑制剂、长效胰岛素和胰岛素输送系统。所有这些药物都能改善血糖控制,并且一些药物已被证明能降低主要心血管结局。在一项关键试验中,司美格鲁肽与 DR 恶化的风险增加约 75%相关。新型长效胰岛素icodec 每周一次给药,与每日一次胰岛素相比,DR 恶化的风险增加。其他最近的抗高血糖药物与 DR 恶化无关,尽管在司美格鲁肽试验之后,几乎所有研究都排除了有预先存在的 DR 的患者。在所有情况下,DR 恶化的病例都很少见。目前正在进行针对司美格鲁肽在 DR 中的安全性的专门研究。
对于大多数考虑使用新型抗高血糖药物治疗的患者,系统代谢和心血管健康方面的益处很可能超过潜在的视网膜危害。尽管由于新药物的安全性数据来自次要终点,因此它们对 DR 的真正风险尚不清楚,但最脆弱的患者是那些有预先存在的高危 DR、基线血糖控制不佳和使用胰岛素的患者。