Diabetes Center, Ohta Nishinouchi Hospital, Koriyama, Japan.
Department of Endocrinology and Metabolism, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
J Diabetes Investig. 2019 Sep;10(5):1318-1331. doi: 10.1111/jdi.13020. Epub 2019 Apr 2.
AIMS/INTRODUCTION: To examine the three-dimensional morphology and vascular endothelial growth factor (VEGF) expression of skin microvasculature in patients with type 2 diabetes in relation to neuropathy, retinopathy and nephropathy.
The present study enrolled 17 individuals with type 2 diabetes and 16 without. Skin sections were double-immunostained for type IV collagen and VEGF-A or protein gene product 9.5. Projected images from confocal microscopy served to quantify the occupancy rate of subepidermal type IV collagen-immunoreactive microvascular basement membrane area (OR-T4MBM), subepidermal VEGF-A-immunoreactive area and the VEGF/T4MBM ratio, as well as the protein gene product 9.5-immunoreactive intraepidermal nerve fiber density. Reduced intraepidermal nerve fiber density was applied for the diagnosis of neuropathy, fundic ophthalmoscopy and fluorescein angiography for retinopathy, and microalbuminuria or persistent proteinuria for nephropathy.
A total of 12 patients with diabetes had neuropathy, 10 had retinopathy and eight had nephropathy. Regardless of the presence or absence of neuropathy, retinopathy or nephropathy, OR-T4MBM was significantly increased in patients with diabetes compared with individuals without diabetes. In contrast, VEGF/T4MBM ratio was significantly decreased in those with neuropathy and retinopathy, as well as in those with and without nephropathy, whereas a trend toward a decreased VEGF/T4MBM ratio was seen in patients without retinopathy, as compared with individuals without diabetes.
The present study is the first report to show that cutaneous microangiopathy, as indicated by subepidermal microvascular proliferation and impaired VEGF expression, appears to occur before the development of overt clinical neuropathy, retinopathy or nephropathy in patients with type 2 diabetes.
目的/引言:本研究旨在探讨 2 型糖尿病患者皮肤微血管的三维形态和血管内皮生长因子(VEGF)表达与神经病变、视网膜病变和肾病的关系。
本研究纳入了 17 名 2 型糖尿病患者和 16 名非糖尿病患者。皮肤切片行 IV 型胶原和 VEGF-A 或蛋白基因产物 9.5 的双重免疫染色。共聚焦显微镜的投影图像用于定量测量表皮下 IV 型胶原免疫反应性微血管基底膜面积(OR-T4MBM)、表皮下 VEGF-A 免疫反应性面积和 VEGF/T4MBM 比值以及蛋白基因产物 9.5 免疫反应性表皮内神经纤维密度。表皮内神经纤维密度减少用于诊断神经病变,眼底检查和荧光血管造影用于诊断视网膜病变,微量白蛋白尿或持续性蛋白尿用于诊断肾病。
共有 12 名糖尿病患者患有神经病变,10 名患有视网膜病变,8 名患有肾病。无论是否存在神经病变、视网膜病变或肾病,糖尿病患者的 OR-T4MBM 均明显高于非糖尿病患者。相比之下,患有神经病变和视网膜病变的患者以及患有和不患有肾病的患者的 VEGF/T4MBM 比值明显降低,而没有视网膜病变的患者的 VEGF/T4MBM 比值呈降低趋势,与非糖尿病患者相比。
本研究首次报道表明,2 型糖尿病患者在出现明显的临床神经病变、视网膜病变或肾病之前,皮肤微血管病变(表现为表皮下微血管增殖和 VEGF 表达受损)可能已经发生。