Mason Ryan H, Minaker Samuel A, Lahaie Luna Gabriela, Bapat Priya, Farahvash Armin, Garg Anubhav, Bhambra Nishaant, Muni Rajeev H
Department of Ophthalmology, St. Michael's Hospital/Unity Health Toronto, Toronto, ON; Department of Ophthalmology & Vision Sciences, University of Toronto, Toronto, ON; Kensington Vision and Research Centre, Toronto, ON.
Department of Ophthalmology, Queen's University, Kingston, ON.
Can J Ophthalmol. 2025 Feb;60(1):e100-e116. doi: 10.1016/j.jcjo.2024.05.031. Epub 2024 Jul 21.
Diabetic retinopathy is a complication of diabetes mellitus with the potential for significant patient morbidity. Although changes to intraocular inflammatory cytokines are integral to disease pathogenesis, studies have been inconsistent about which exact cytokines are associated with diabetic retinopathy. We aimed to quantitatively summarize proangiogenic and proinflammatory cytokines in nonproliferative diabetic retinopathy (NPDR), given its frequency among those with diabetes mellitus.
A systematic literature search without year limitation to February 21, 2022, identified 59 studies assessing vitreous or aqueous cytokine levels in NPDR, encompassing 1378 eyes with NPDR and 1288 eyes from nondiabetic controls. Effect sizes were generated as standardized mean differences (SMD) of cytokine concentrations between patients with NPDR and controls.
Concentrations (SMD, 95% confidence interval, and p value) of aqueous interleukin-6 (IL-6) (2.58, 1.17-3.99; p = 0.0003), IL-8 (1.56, 0.39-2.74; p = 0.009), IL-17 (13.55, 7.50-19.59; p < 0.001), transforming growth factor beta (TGF-β) (2.44, 1.02-3.85; p = 0.0007) and vascular endothelial growth factor (VEGF) (1.35, 0.76-1.93; p < 0.00001), and vitreous VEGF (1.49, 0.60-2.37; p = 0.001) were significantly higher in patients with NPDR when compared with those of healthy controls.
These cytokines may serve as disease markers of the biochemical alterations seen in NPDR and may guide interventions, as we move into an era of more targeted therapeutics.
糖尿病视网膜病变是糖尿病的一种并发症,具有导致患者出现严重发病情况的可能性。尽管眼内炎性细胞因子的变化是疾病发病机制的重要组成部分,但关于哪些确切的细胞因子与糖尿病视网膜病变相关,研究结果并不一致。鉴于非增殖性糖尿病视网膜病变(NPDR)在糖尿病患者中较为常见,我们旨在对其促血管生成和促炎细胞因子进行定量总结。
进行无年份限制直至2022年2月21日的系统文献检索,共识别出59项评估NPDR患者玻璃体液或房水细胞因子水平的研究,其中包括1378只患有NPDR的眼睛和1288只来自非糖尿病对照者的眼睛。效应量以NPDR患者与对照者之间细胞因子浓度的标准化平均差(SMD)表示。
与健康对照者相比,NPDR患者房水中白细胞介素-6(IL-6)(2.58,1.17 - 3.99;p = 0.0003)、IL-8(1.56,0.39 - 2.74;p = 0.009)、IL-17(13.55,7.50 - 19.59;p < 0.001)、转化生长因子β(TGF-β)(2.44,1.02 - 3.85;p = 0.0007)和血管内皮生长因子(VEGF)(1.35,0.76 - 1.93;p < 0.00001)以及玻璃体液中VEGF(1.49,0.60 - 2.37;p = 0.001)的浓度显著更高。
随着我们进入一个更具针对性治疗的时代,这些细胞因子可能作为NPDR中所见生化改变的疾病标志物,并可能指导干预措施。