Natividade Gabriella R, Spiazzi Bernardo F, Baumgarten Matheus W, Bassotto Caroline, Pereira Afonso A, Fraga Bruna L, Scalco Bruno G, Mattes Nicole R, Lavinsky Daniel, Kramer Caroline K, Gerchman Fernando
Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Post-graduate Program in Medical Sciences: Endocrinology, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
JAMA Ophthalmol. 2025 Aug 14. doi: 10.1001/jamaophthalmol.2025.2489.
Semaglutide is a widely used treatment for diabetes and obesity, offering considerable cardiovascular benefit. However, its association with ocular adverse events remains uncertain.
To assess the incidence of eye disorders, diabetic retinopathy, and nonarteritic anterior ischemic optic neuropathy (NAION) in adults treated with semaglutide.
A comprehensive electronic search of PubMed, Embase, and the Cochrane Central Register of Controlled Trials was conducted on April 10, 2025, without date restrictions.
Investigators independently screened records to identify randomized clinical trials comparing semaglutide with either an active comparator or placebo in adults, assessing ocular adverse events.
Descriptive synthesis of the included studies was performed. The random-effects model using the inverse variance method was used to summarize the odds ratio (OR) for eye disorders and diabetic retinopathy. Peto OR with a fixed-effects model was applied for NAION. Risk of bias was assessed with the RoB 2.0 tool and quality of evidence with GRADE. Trial sequential analysis (TSA) was performed to determine whether the available data were sufficient for definitive conclusions.
The primary outcomes included the number of patients experiencing an ocular adverse event, diabetic retinopathy, or NAION. Subgroup analyses were conducted based on follow-up duration, comparator type, and primary baseline condition.
A total of 78 trials with 73 640 participants were included. Semaglutide did not increase or reduce the risk of eye disorders (OR, 1.01; 95% CI, 0.91-1.12) or diabetic retinopathy (OR, 1.04; 95% CI, 0.92-1.17). Treatment with semaglutide was associated with a significant odds of NAION (OR, 3.92; 95% CI, 1.02-15.02). Overall risk of bias was low. TSA provided evidence that the sample size was sufficient to avoid missing alternative results for diabetic retinopathy but not for NAION.
These findings suggest that semaglutide was not associated with an increased risk of eye disorders or diabetic retinopathy. Despite the fact that an association between semaglutide treatment and NAION was found, current evidence remains insufficient to establish definitive conclusions regarding its association with NAION. Further studies with larger sample sizes and adequate evaluation of NAION are warranted to clarify this potential risk.
司美格鲁肽是一种广泛用于治疗糖尿病和肥胖症的药物,具有显著的心血管益处。然而,其与眼部不良事件的关联仍不确定。
评估接受司美格鲁肽治疗的成年人中眼部疾病、糖尿病视网膜病变和非动脉炎性前部缺血性视神经病变(NAION)的发生率。
于2025年4月10日对PubMed、Embase和Cochrane对照试验中央注册库进行了全面的电子检索,无日期限制。
研究人员独立筛选记录,以确定在成年人中比较司美格鲁肽与活性对照药或安慰剂,并评估眼部不良事件的随机临床试验。
对纳入的研究进行描述性合成。采用逆方差法的随机效应模型总结眼部疾病和糖尿病视网膜病变的比值比(OR)。NAION采用固定效应模型的Peto OR。使用RoB 2.0工具评估偏倚风险,使用GRADE评估证据质量。进行试验序贯分析(TSA)以确定现有数据是否足以得出明确结论。
主要结局包括发生眼部不良事件、糖尿病视网膜病变或NAION的患者数量。根据随访时间、对照类型和主要基线状况进行亚组分析。
共纳入78项试验,73640名参与者。司美格鲁肽未增加或降低眼部疾病(OR,1.01;95%CI,0.91-1.12)或糖尿病视网膜病变(OR,1.04;95%CI,0.92-1.17)的风险。司美格鲁肽治疗与NAION的显著比值比相关(OR,3.�2;95%CI,1.02-15.02)。总体偏倚风险较低。TSA提供的证据表明,样本量足以避免遗漏糖尿病视网膜病变的替代结果,但对于NAION则不足。
这些发现表明,司美格鲁肽与眼部疾病或糖尿病视网膜病变风险增加无关。尽管发现司美格鲁肽治疗与NAION之间存在关联,但目前的证据仍不足以就其与NAION的关联得出明确结论。需要进行更大样本量且对NAION进行充分评估的进一步研究,以阐明这种潜在风险。