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眼内液中血管生成和炎症标志物在糖尿病性黄斑水肿中的作用及贝伐单抗治疗的影响。

Angiogenic and inflammatory markers in the intraocular fluid of eyes with diabetic macular edema and influence of therapy with bevacizumab.

机构信息

Department of Ophthalmology, Medical University of Vienna, Vienna, Austria.

出版信息

Retina. 2010 Oct;30(9):1412-9. doi: 10.1097/IAE.0b013e3181e095c0.

DOI:10.1097/IAE.0b013e3181e095c0
PMID:20711086
Abstract

PURPOSE

The purpose of this study was to determine the concentrations of angiogenic and inflammatory markers in human eyes with diffuse diabetic macular edema before and during therapy with intravitreal bevacizumab and their association with disease activity.

METHODS

In a prospective clinical trial, 10 eyes of 10 consecutive patients with vision loss because of diabetic macular edema were compared with 10 eyes of 10 age-matched controls. Bevacizumab was administered at baseline; retreatments were given monthly according to disease activity. During a follow-up of 6 months, aqueous humor samples were taken each time intravitreal therapy was administered. A multiplex assay was used for measurement of 12 different growth factors and cytokines.

RESULTS

Aqueous humor of eyes with diabetic macular edema demonstrated a significantly increased expression of monocyte chemoattractant protein-1 and interleukin-8 and higher, but not significant, levels of interleukin-6 and vascular endothelial growth factor. Intravitreal therapy with bevacizumab resulted in a significant decrease of vascular endothelial growth factor below physiologic levels. This change was not associated with clinical disease activity as measured by visual acuity and central retinal thickness.

CONCLUSION

Eyes with diabetic macular edema showed a different profile of monocyte chemoattractant protein-1 and interleukin-8 as compared with controls. The intraocular vascular endothelial growth factor expression decreased significantly after the first intravitreal injection of bevacizumab; this reduction was prolonged by consecutive monthly retreatment.

摘要

目的

本研究旨在测定弥漫性糖尿病黄斑水肿患者眼内血管生成和炎症标志物的浓度,及其与疾病活动的相关性。

方法

在一项前瞻性临床试验中,将 10 例因糖尿病黄斑水肿而视力丧失的患者(共 10 只眼)与 10 例年龄匹配的对照者(共 10 只眼)进行比较。在基线时给予贝伐单抗治疗;根据疾病活动度,每月进行一次治疗。在 6 个月的随访期间,每次玻璃体内治疗时采集房水样本。采用多重分析检测 12 种不同的生长因子和细胞因子。

结果

糖尿病黄斑水肿眼房水中的单核细胞趋化蛋白-1 和白细胞介素-8表达显著增加,白细胞介素-6 和血管内皮生长因子水平较高,但无统计学意义。玻璃体内注射贝伐单抗可显著降低血管内皮生长因子至生理水平以下。这种变化与视力和中心视网膜厚度测量的临床疾病活动无关。

结论

与对照组相比,糖尿病黄斑水肿眼表现出不同的单核细胞趋化蛋白-1 和白细胞介素-8特征。首次玻璃体内注射贝伐单抗后,眼内血管内皮生长因子表达显著下降;连续每月进行治疗可延长这种下降。

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