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视黄醇结合蛋白 3 浓度升高与玻璃体炎症细胞因子、VEGF 降低及糖尿病视网膜病变进展有关。

Elevated Retinol Binding Protein 3 Concentrations Are Associated With Decreased Vitreous Inflammatory Cytokines, VEGF, and Progression of Diabetic Retinopathy.

机构信息

Research Division, Joslin Diabetes Center, Boston, MA.

Beetham Eye Institute, Joslin Diabetes Center, Boston, MA.

出版信息

Diabetes Care. 2022 Sep 1;45(9):2159-2162. doi: 10.2337/dc22-0165.

Abstract

OBJECTIVE

To correlate inflammatory cytokines and vascular endothelial growth factor (VEGF) in vitreous and plasma with vitreous retinol binding protein 3 (RBP3), diabetic retinopathy (DR) severity, and DR worsening in a population with type 1 and type 2 diabetes.

RESEARCH DESIGN AND METHODS

RBP3, VEGF, and inflammatory cytokines were measured in plasma and vitreous samples (n = 205) from subjects of the Joslin Medalist Study and Beetham Eye Institute.

RESULTS

Higher vitreous RBP3 concentrations were associated with less severe DR (P < 0.0001) and a reduced risk of developing proliferative DR (PDR) (P < 0.0001). Higher RBP3 correlated with increased photoreceptor segment thickness and lower vitreous interleukin-12 (IL-12), tumor necrosis factor-α (TNF-α), and TNF-β (P < 0.05). PDR was associated with lower vitreous interferon-γ and IL-10 and higher VEGF, IL-6, and IL-15 (P < 0.05), but was not associated with their plasma concentrations.

CONCLUSIONS

Higher vitreous RBP3 concentrations are associated with less severe DR and slower rates of progression to PDR, supporting its potential as a biomarker and therapeutic agent for preventing DR worsening, possibly by lowering retinal VEGF and inflammatory cytokines.

摘要

目的

在 1 型和 2 型糖尿病患者中,将玻璃体和血浆中的炎症细胞因子和血管内皮生长因子(VEGF)与玻璃体视黄醇结合蛋白 3(RBP3)相关联,以评估其与糖尿病视网膜病变(DR)严重程度和 DR 恶化的关系。

研究设计与方法

在 Joslin Medalist 研究和 Beetham 眼科研究所的受试者玻璃体和血浆样本(n = 205)中测量 RBP3、VEGF 和炎症细胞因子。

结果

较高的玻璃体 RBP3 浓度与较不严重的 DR(P < 0.0001)和降低发生增生性 DR(PDR)的风险相关(P < 0.0001)。较高的 RBP3 与光感受器节段厚度增加和玻璃体白细胞介素-12(IL-12)、肿瘤坏死因子-α(TNF-α)和 TNF-β 降低相关(P < 0.05)。PDR 与玻璃体干扰素-γ和 IL-10 降低以及 VEGF、IL-6 和 IL-15 升高相关(P < 0.05),但与它们的血浆浓度无关。

结论

较高的玻璃体 RBP3 浓度与较不严重的 DR 相关,并且向 PDR 进展的速度较慢,支持其作为预防 DR 恶化的生物标志物和治疗剂的潜力,可能通过降低视网膜 VEGF 和炎症细胞因子来实现。

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