血浆色素上皮衍生因子浓度与糖尿病视网膜病变的关系

Tayfun Şahin, A. Karabulut
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摘要

目的糖尿病视网膜病变(Diabetic retinopathy, DRP)是糖尿病最常见的微血管并发症之一。色素上皮衍生因子(PEDF)是一种蛋白质,是最有效的血管生成抑制剂之一。血液PEDF浓度对DRP形成的影响尚不清楚。本研究旨在确定血浆PEDF浓度是否对DRP的出现有影响。方法选取62例糖尿病患者和20例健康对照者。患者组包括非增殖性DRP 28例,增殖性DRP 13例,非增殖性DRP 21例。采用ELISA法检测患者血清中PEDF水平。计算参与者的身体质量指数。结果糖尿病患者血清PEDF水平(1.533±0.233 μg/mL)低于健康组(2.163±0.343 μg/mL) (p=0.002)。DRP组和非DRP组PEDF水平相似(p=0.337)。血浆PEDF水平随DRP的进展而降低(p=0.001)。结论血中PEDF浓度随DRP分级的升高而降低。PEDF血药浓度降低可能是预测微血管并发症的重要指标。在不久的将来,含PEDF的药物可能用于眼内/全身治疗目的,以预防糖尿病的血管并发症。
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The association between plasma concentration of pigment epithelium-derived factor and diabetic retinopathy
Abstract Objectives Diabetic retinopathy (DRP) is one of the most common microvascular complications of diabetes. The pigment epithelium-derived factor (PEDF) is a protein that is one of the most potent angiogenesis inhibitors. The effect of blood PEDF concentration on DRP formation remains unclear. The present study aimed to determine whether the plasma concentration of PEDF is effective on the appearance of DRP. Methods The present study consisted of 62 patients with diabetes mellitus and 20 healthy participants. The patient group included 28 patients with non-proliferative DRP, 13 with proliferative DRP, and 21 diabetic patients without DRP. The PEDF levels in patient serum samples were detected through the ELISA method. The body mass index of the participants was calculated. Results Serum PEDF levels of diabetic patients (1.533 ± 0.233 μg/mL) were found to be lower (2.163 ± 0.343 μg/mL) than healthy participants (p=0.002). The PEDF levels were similar in the DRP and non-DRP groups (p=0.337). The plasma PEDF level decreased along with the progression of DRP (p=0.001). Conclusions The PEDF concentration in the blood decreases along with the increase of DRP grade. Decreased blood concentration of PEDF may be important to predict microvascular complications. Agents containing PEDF may be used intraocularly/systemically for therapeutic purposes to prevent vascular complications of diabetes in the near future.
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