Cao J, McLeod S, Merges C A, Lutty G A
Wilmer Ophthalmological Institute, The Johns Hopkins Hospital, Baltimore, MD 21287-9115, USA.
Arch Ophthalmol. 1998 May;116(5):589-97. doi: 10.1001/archopht.116.5.589.
To measure the extent of choriocapillaris degeneration (CCD) in diabetic choroids and to study the association of CCD with choroidal neovascularization and pathologic changes in Bruch's membrane-like basal laminar deposits.
Human choroids from 10 postmortem subjects (diabetic, 5 [group 1]; nondiabetic, 5 [group 2]) were incubated for the histochemical demonstration of alkaline phosphatase and nonspecific esterase activities, permitting analysis of the choroidal vasculature and polymorphonuclear leukocytes, respectively. The tissue was then flat embedded and sectioned for structural analysis. Areas of CCD were measured in the flat perspective by computer-assisted image analysis and verified in cross-sections of flat-embedded tissue.
The CCD in choroids from subjects with diabetes (group 1) appeared in 2 patterns: diffuse (partial loss of alkaline phosphatase activity in a poorly defined area, ie, degeneration of some capillary segments) and focal (complete degeneration of choriocapillaris or loss of alkaline phosphatase activity in a relatively well-defined area). The mean+/-SD percentage of the choroid with focal CCD in group 1 was 5.08%+/-1.13% of the total choroidal area vs 1. 16%+/-0.35% in group 2 (P<.001). Focal CCD in group 1 was more prominent in the posterior pole than in the peripheral choroid. Choroidal neovascularization was associated with some areas of diffuse CCD in group 1. Pathologic changes in Bruch's membrane-like basal laminar deposits were often associated with CCD; the thickness of the deposits was greater in group 1 than in group 2 and greater in areas with focal CCD than in areas with diffuse or no CCD.
The percentage of choroid with focal CCD in group 1 choroids was more than 4-fold greater than that in nondiabetic choroids. The presence of CCD was related to basal laminar deposits and, in some cases, to choroidal neovascularization.
测量糖尿病脉络膜中脉络膜毛细血管变性(CCD)的程度,并研究CCD与脉络膜新生血管形成以及布鲁赫膜样基底膜沉积物病理变化之间的关联。
对10例死后受试者(糖尿病患者5例[第1组];非糖尿病患者5例[第2组])的人脉络膜进行孵育,以进行碱性磷酸酶和非特异性酯酶活性的组织化学显示,分别用于分析脉络膜血管系统和多形核白细胞。然后将组织进行平铺包埋并切片用于结构分析。通过计算机辅助图像分析在平铺视野中测量CCD区域,并在平铺包埋组织的横截面中进行验证。
糖尿病患者(第1组)脉络膜中的CCD呈现两种模式:弥漫性(在边界不清的区域碱性磷酸酶活性部分丧失,即一些毛细血管段变性)和局灶性(脉络膜毛细血管完全变性或在相对边界清晰的区域碱性磷酸酶活性丧失)。第1组中局灶性CCD占脉络膜总面积的平均±标准差百分比为5.08%±1.13%,而第2组为1.16%±0.35%(P<0.001)。第1组中的局灶性CCD在黄斑后极比周边脉络膜更明显。脉络膜新生血管形成与第1组中的一些弥漫性CCD区域相关。布鲁赫膜样基底膜沉积物的病理变化常与CCD相关;第1组沉积物的厚度大于第2组,且局灶性CCD区域的沉积物厚度大于弥漫性或无CCD区域。
第1组脉络膜中局灶性CCD的百分比比非糖尿病脉络膜中的高出4倍多。CCD的存在与基底膜沉积物有关,在某些情况下,与脉络膜新生血管形成有关。