The Effect of Glucagon-Like Peptide-1 Receptor Agonists on Diabetic Retinopathy at a Tertiary Care Center

IF 3.2 Q1 OPHTHALMOLOGY
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引用次数: 0

Abstract

Objective

The potential association between diabetic retinopathy (DR) worsening and glucagon-like peptide-1 receptor agonists (GLP-1RA) has affected therapeutic management of diabetic patients but remains controversial. This study compared rates of DR development or progression in patients on GLP-1RA to those on SGLT-2 inhibitors (SGLT-2I).

Design

Retrospective cohort study.

Subjects

Nine hundred eighty-one patients with diabetes mellitus taking GLP-1RA or SGLT-2I, the latter serving as controls, between 2012 and 2023.

Methods

Patients were one-to-one greedy matched by propensity scores on race/ethnicity, age, smoking status, baseline body mass index and hemoglobin A1c %, type of diabetes mellitus, baseline DR status and history of DR procedures, duration of drug use, whether they had taken both drug types, and change in hemoglobin A1c % after 1 year on the drug.

Main Outcome Measures

The primary outcome was clinical DR development or progression (termed “worsening”) detected by International Classification of Diseases (ICD), 10th edition codes, confirmed by manual review, on GLP-1RA compared with SGLT-2I after propensity score matching. Secondary outcomes included DR worsening indicated by need for procedures due to complications, and time-to-first DR worsening event.

Results

The study included 692 GLP-1RA users and 289 SGLT-2I users. The mean follow-up periods for GLP-1RA versus SGLT-2I use were 1.54 (standard deviation [SD] 1.82) years and 1.38 (SD 1.56) years, respectively. The rates of clinical worsening were 2.3% and 2.8%, respectively. After propensity score matching, an association was not identified between GLP1-RA and DR worsening neither clinically by ICD-10 codes (odds ratio [OR] = 0.33, 95% confidence interval [CI]: 0.11–1.03) nor by indication for procedures (OR = 0.50, 95% CI 0.13–2.00). Time-to-first DR worsening did not differ between the groups in Kaplan-Meier analysis. The most common type of clinical worsening event for both drug types was vitreous hemorrhage (43.7% and 50% of worsening events in GLP-1RA and SGLT-2I users, respectively). The most common DR procedure indicated was anti-VEGF injections (34% and 35% of GLP-1RA and SGLT-2I events, respectively).

Conclusions

Diabetic retinopathy worsening, either clinically or by procedures, was not associated with GLP-1RA compared with SGLT-2I, both before and after propensity score matching on all analyses, including time-to-first worsening event.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

GLP-1 受体激动剂对一家三级医疗中心糖尿病视网膜病变的影响
目的糖尿病视网膜病变(DR)恶化与胰高血糖素样肽-1 受体激动剂(GLP-1RA)之间的潜在关联影响了糖尿病患者的治疗管理,但目前仍存在争议。本研究比较了服用 GLP-1RA 和服用 SGLT-2 抑制剂 (SGLT-2I) 患者的 DR 发生率或进展率。方法对患者的种族/民族、年龄、吸烟状况、基线体重指数和血红蛋白A1c%、糖尿病类型、基线DR状况和DR手术史、用药时间、是否同时服用两种药物以及用药1年后血红蛋白A1c%的变化进行倾向得分一对一贪婪匹配。主要结果测量主要结果是与 SGLT-2I 相比,GLP-1RA 与 SGLT-2I 经倾向得分匹配后,通过国际疾病分类 (ICD) 第 10 版代码发现的临床 DR 发展或进展(称为 "恶化"),并通过人工复查确认。次要结果包括因并发症而需要进行手术的DR恶化,以及首次DR恶化事件发生的时间。GLP-1RA 和 SGLT-2I 的平均随访时间分别为 1.54 年(标准差 [SD] 1.82)和 1.38 年(标准差 1.56)。临床恶化率分别为2.3%和2.8%。经过倾向评分匹配后,无论是按 ICD-10 编码(比值比 [OR] = 0.33,95% 置信区间 [CI]:0.11-1.03)还是按手术指征(比值比 [OR] = 0.50,95% 置信区间 [CI]:0.13-2.00),都未发现 GLP1-RA 与 DR 临床恶化之间存在关联。在 Kaplan-Meier 分析中,两组患者的 DR 首次恶化时间没有差异。两种药物最常见的临床恶化事件类型均为玻璃体出血(分别占 GLP-1RA 和 SGLT-2I 使用者恶化事件的 43.7% 和 50%)。结论与SGLT-2I相比,GLP-1RA和SGLT-2I在临床或手术方面的糖尿病视网膜病变恶化与倾向得分匹配前后的所有分析(包括首次恶化事件发生时间)均无关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ophthalmology science
Ophthalmology science Ophthalmology
CiteScore
3.40
自引率
0.00%
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审稿时长
89 days
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