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糖尿病视网膜病变患者房水中血管内皮生长因子(VEGF)和可溶性VEGF受体-1的浓度。

Aqueous concentrations of VEGF and soluble VEGF receptor-1 in diabetic retinopathy patients.

作者信息

Javanmard Shaghayegh Haghjooy, Hasanpour Zahra, Abbaspoor Zahra, Naderian Gholam A, Jahanmard Mehdi

机构信息

Department of Physiology, Physiology Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

J Res Med Sci. 2012 Dec;17(12):1124-7.

Abstract

BACKGROUND

The aim of this study was to simultaneously measure the concentrations of vascular endothelial growth factor (VEGF) and soluble VEGF receptor-1 (sVEGFR-1, also known as sFlt-1) in the aqueous humor of patients with non-proliferative diabetic retinopathy (NPDR) and to investigate whether aqueous levels of vascular endothelial growth factor (VEGF) and VEGFR-1 are related to diabetic macular edema.

MATERIALS AND METHODS

Aqueous humor was collected from 27 diabetic patients and 33 age- and sex-matched normoglycemic controls and analyzed for pro-angiogenic VEGF and angiogenic inhibitor VEGFR-1 by enzyme-linked immunosorbent assay (ELISA). The mean foveal thickness was measured by optical coherence tomography (OCT).

RESULTS

There was no significant difference in the aqueous levels of VEGF in patients with NPDR compared with control subjects (P > 0.05), while the NPDR patients had significantly lower sVEGFR-1 in their aqueous humor. Furthermore, a significant (P < 0.01) positive correlation was observed between VEGF/sVEGFR-1 concentration and the mean foveal thickness measured on OCT.

CONCLUSION

The results suggest that decreased chelating effect of sVEGFR-1 may be the preliminary event allowing VEGF to activate the proangiogenic endothelial cell state and to induce permeability. The imbalance between angiogenic agent (VEGF) and the antiangiogenic factors (sFlt-1), which is disturbed in the diabetic state, may determine the fate of diabetic macular edema.

摘要

背景

本研究的目的是同时测量非增殖性糖尿病视网膜病变(NPDR)患者房水中血管内皮生长因子(VEGF)和可溶性VEGF受体-1(sVEGFR-1,也称为sFlt-1)的浓度,并研究房水中血管内皮生长因子(VEGF)和VEGFR-1水平是否与糖尿病性黄斑水肿相关。

材料与方法

收集27例糖尿病患者和33例年龄及性别匹配的血糖正常对照者的房水,采用酶联免疫吸附测定(ELISA)分析促血管生成的VEGF和血管生成抑制剂VEGFR-1。通过光学相干断层扫描(OCT)测量平均黄斑中心凹厚度。

结果

与对照组相比,NPDR患者房水中VEGF水平无显著差异(P>0.05),而NPDR患者房水中sVEGFR-1显著降低。此外,观察到VEGF/sVEGFR-1浓度与OCT测量的平均黄斑中心凹厚度之间存在显著正相关(P<0.01)。

结论

结果表明,sVEGFR-1螯合作用降低可能是使VEGF激活促血管生成内皮细胞状态并诱导通透性的初始事件。血管生成剂(VEGF)与抗血管生成因子(sFlt-1)之间的失衡在糖尿病状态下受到干扰,可能决定糖尿病性黄斑水肿的转归。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b5/3703163/2f2c2199d018/JRMS-17-1124-g002.jpg

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