Supplementary Material for: High Vitreous Concentration of IL-6 and IL-8, but Not of Adhesion Molecules in Relation to Plasma Concentrations in Proliferative Diabetic Retinopathy
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https://karger.figshare.com/articles/dataset/Supplementary_Material_for_High_Vitreous_Concentration_of_IL-6_and_IL-8_but_Not_of_Adhesion_Molecules_in_Relation_to_Plasma_Concentrations_in_Proliferative_Diabetic_Retinopathy/5124097
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<b><i>Background/Aim:</i></b> Inflammatory markers have been observed in proliferative diabetic retinopathy (PDR). We assessed vitreous concentrations of adhesion molecules and cytokines in PDR and non-diabetic controls and plasma concentrations to differentiate local inflammation from the breakdown of the blood-retina barrier. <b><i>Methods:</i></b> 38 patients with PDR and 16 controls with macular hole or epiretinal membrane underwent vitrectomy. Vitreous and plasma soluble adhesion molecules [sE-selectin, intercellular adhesion molecule (sICAM)-1 and -3, platelet-endothelial cell adhesion molecule (sPECAM)-1, sP-selectin, vascular cell adhesion molecule (sVCAM)-1] and cytokines [interleukin (IL)-1β, IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12 (p70), tumour necrosis factor-α and -β, γ-interferon] were detected by the multiplex assay. <b><i>Results:</i></b> Levels of IL-6 and IL-8 were 26-fold (p = 0.001) and 6-fold higher (p = 0.001) in vitreous than in plasma in PDR. Vitreous IL-10 (p = 0.004), sPECAM-1, sE-selectin, sICAM-1 and sVCAM-1 were higher in PDR than controls (p = 0.001 for all). Adhesion molecule concentrations in vitreous in PDR were less than 10% of those in plasma. IL-10 was lower in vitreous than plasma (3.0 vs. 12.8 pg/ml, p = 0.007), and the vitreous IL-10/IL-8 ratio was significantly lower in PDR than in controls (0.10 vs. 0.55 pg/ml, p = 0.003). <b><i>Conclusion:</i></b> The elevated IL-6 and IL-8 levels in vitreous, but not in plasma, are evidence favouring local over systemic inflammation in PDR. Furthermore, there was imbalance between inflammatory and anti-inflammatory cytokines in the vitreous.
**背景与研究目的:** 已有研究在增生性糖尿病视网膜病变(proliferative diabetic retinopathy, PDR)中观察到炎症标志物。本研究旨在检测PDR患者与非糖尿病对照受试者的玻璃体黏附分子与细胞因子浓度,并检测血浆浓度,以区分局部炎症与血视网膜屏障(blood-retina barrier)破坏。
**方法:** 38例PDR患者及16例伴有黄斑裂孔或视网膜前膜的对照受试者接受了玻璃体切割术。采用多重检测法对玻璃体与血浆中的可溶性黏附分子[可溶性E-选择素(sE-selectin)、细胞间黏附分子(sICAM)-1与-3、血小板-内皮细胞黏附分子(sPECAM)-1、可溶性P-选择素(sP-selectin)、血管细胞黏附分子(sVCAM)-1]及细胞因子[白细胞介素(IL)-1β、IL-2、IL-4、IL-5、IL-6、IL-8、IL-10、IL-12(p70)、肿瘤坏死因子-α、-β及γ-干扰素]进行了检测。
**结果:** PDR患者玻璃体中的IL-6与IL-8水平分别较血浆升高26倍(p=0.001)与6倍(p=0.001)。PDR患者玻璃体中的IL-10(p=0.004)、sPECAM-1、sE-selectin、sICAM-1及sVCAM-1水平均高于对照组(所有指标p=0.001)。PDR患者玻璃体中的黏附分子浓度不足血浆中的10%。玻璃体IL-10水平低于血浆(3.0 vs 12.8 pg/ml,p=0.007),且PDR患者的玻璃体IL-10/IL-8比值显著低于对照组(0.10 vs 0.55 pg/ml,p=0.003)。
**结论:** 玻璃体中升高的IL-6与IL-8水平(而非血浆中),为PDR的炎症以局部炎症而非全身炎症为主提供了证据。此外,玻璃体中促炎与抗炎细胞因子存在失衡。
提供机构:
Karger Publishers
创建时间:
2017-06-20



