1型糖尿病合并糖尿病肾病患者血管内皮生长因子升高。

Kidney international. Supplement Pub Date : 2000-04-01
P Hovind, L Tarnow, P B Oestergaard, H H Parving
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引用次数: 0

摘要

背景:生长因子已被认为在糖尿病肾病的发生和发展中发挥作用。血管内皮生长因子(VEGF)是一种有效的细胞因子家族,可诱导血管生成并显著增加内皮细胞的通透性。本研究的目的是调查合并糖尿病肾病的1型糖尿病患者和长期合并尿白蛋白正常的1型糖尿病患者的血浆VEGF水平,并评估VEGF作为肾病进展的预测因子。方法:对199例1型糖尿病合并糖尿病肾病患者(122例男性,年龄41 +/- 10岁,糖尿病病程28 +/- 8年)、肾小球滤过率(GFR)(中位数[范围])75 [10-143]mL/min/1.73 m2,以及188例长期存在的1型糖尿病合并持续性蛋白尿正常患者(115例男性,年龄43 +/- 10岁,糖尿病病程27 +/- 9年)进行了VEGF检测。155例蛋白尿患者在基线检查后进行了至少3年的随访,每年进行GFR测量。结果:与蛋白尿正常组相比,肾病患者血浆VEGF水平显著升高;(中位数[范围])分别为45.7[22.0-410]和27.1 [22.0-355]ng/L, P < 0.001。这种差异归因于肾病男性的VEGF水平升高:51.8[22.0-410]比22.0 [22.0-308]ng/L, P < 0。001. 有和没有肾病的女性之间没有差异:37.8[22.0-325]和36.6 [22.0-335]ng/L, NS。在GFR高于和低于中位数的蛋白尿患者中,VEGF、NS水平无差异。60例肾病患者和93例蛋白尿正常患者血浆VEGF低于检出限(22.0 ng/L), P < 0.001。GFR平均下降率为3.5 (SE: 0.4) mL/min/年,以下基线变量作为进展的预测因子:蛋白尿、平均动脉血压和男性性别。血红蛋白A1c和血浆VEGF不能作为预测因子。在有和没有增生性视网膜病变的患者之间没有发现显著差异。结论:我们的数据表明,在男性1型糖尿病肾病的早期,VEGF升高。基线蛋白尿、动脉血压和男性性别是糖尿病肾病进展的预测因素,而血浆VEGF和血红蛋白A1c没有贡献。VEGF在糖尿病肾病发病中的重要性仍有待确定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Elevated vascular endothelial growth factor in type 1 diabetic patients with diabetic nephropathy.

Background: Growth factors have been suggested to play a role in the development and progression of diabetic nephropathy. Vascular endothelial growth factor (VEGF) is a potent cytokine family that induces angiogenesis and markedly increases endothelial permeability. The aim of the present study was to investigate plasma levels of VEGF in a large cohort of type 1 diabetic patients with diabetic nephropathy and in long-standing type 1 diabetic patients with persistent normoalbuminuria, and to evaluate VEGF as a predictor of nephropathy progression.

Methods: We measured VEGF with an enzyme-linked immunosorbent assay (ELISA) technique in 199 type 1 diabetic patients with diabetic nephropathy (122 males, age 41 +/- 10 years, diabetes duration 28 +/- 8 years), glomerular filtration rate (GFR) (median [range]) 75 [10-143] mL/min/1.73 m2, and in 188 long-standing type 1 diabetic patients with persistent normoalbuminuria (115 males, age 43 +/- 10 years, diabetes duration 27 +/- 9 years). One hundred fifty-five of the proteinuric patients were followed for at least 3 years after baseline examination with yearly GFR measurements.

Results: Plasma levels of VEGF were significantly increased in patients with nephropathy as compared to the normoalbuminuric group; (median [range]): 45.7 [22.0-410] versus 27.1 [22.0-355] ng/L, respectively, P < 0.001. This difference was ascribed to elevated VEGF levels in nephropathic men: 51.8 [22.0-410] versus 22.0 [22.0-308] ng/L, P < 0. 001. No differences were found between women with and without nephropathy: 37.8 [22.0-325] versus 36.6 [22.0-335] ng/L, NS. In proteinuric patients with GFR above and below the median value, there was no difference in the level of VEGF, NS. Plasma VEGF was below the detection limit (22.0 ng/L) in 60 patients with nephropathy and 93 patients with normoalbuminuria, P < 0.001. The mean rate of GFR decline was 3.5 (SE: 0.4) mL/min/year, and the following baseline variables acted as predictors of progression: albuminuria, mean arterial blood pressure and male gender. Hemoglobin A1c and plasma VEGF did not act as predictors. No significant differences between patients with and without proliferative retinopathy were detected.

Conclusions: Our data suggest that VEGF is elevated early in the course of diabetic nephropathy in men with type 1 diabetes mellitus. Baseline albuminuria, arterial blood pressure and male gender was predictors of diabetic nephropathy progression, while plasma VEGF and Hemoglobin A1c did not contribute. The importance of VEGF in the initiation of diabetic nephropathy remains to be established.

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