非增殖性糖尿病视网膜病变中水样和玻璃体炎症细胞因子水平的变化:系统综述和荟萃分析。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-07-21 DOI:10.1016/j.jcjo.2024.05.031
Ryan H Mason, Samuel A Minaker, Gabriela Lahaie Luna, Priya Bapat, Armin Farahvash, Anubhav Garg, Nishaant Bhambra, Rajeev H Muni
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引用次数: 0

摘要

目的:糖尿病视网膜病变是糖尿病的一种并发症,可能导致患者严重发病。虽然眼内炎症细胞因子的变化与疾病的发病机制密不可分,但关于究竟哪些细胞因子与糖尿病视网膜病变有关的研究却不一致。鉴于非增殖性糖尿病视网膜病变(NPDR)在糖尿病患者中的发病率较高,我们旨在定量总结非增殖性糖尿病视网膜病变(NPDR)中的促血管生成细胞因子和促炎症细胞因子:截至 2022 年 2 月 21 日的一项无年份限制的系统性文献检索发现了 59 项评估非增殖性糖尿病视网膜病变玻璃体或水样细胞因子水平的研究,其中包括 1378 例非增殖性糖尿病视网膜病变患者和 1288 例非糖尿病对照患者。结果显示,NPDR 患者与对照组之间细胞因子浓度的标准化平均差 (SMD) 为效应大小:眼白细胞介素-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.与健康对照组相比,NPDR 患者的IL(13.55,7.50-17.59;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VEGF(1.49,0.60-2.37;P=0.001)显著升高:这些细胞因子可作为 NPDR 生化改变的疾病标志物,并可在我们进入更具针对性的治疗时代时为干预措施提供指导。
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Changes in aqueous and vitreous inflammatory cytokine levels in nonproliferative diabetic retinopathy: systematic review and meta-analysis.

Objective: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

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7.20
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4.30%
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567
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