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母系遗传的糖尿病和耳聋以及弹性假黄瘤中的脉络膜毛细血管信号缺失

CHORIOCAPILLARIS SIGNAL VOIDS IN MATERNALLY INHERITED DIABETES AND DEAFNESS AND IN PSEUDOXANTHOMA ELASTICUM.

作者信息

Spaide Richard F

机构信息

Vitreous, Retina, Macula Consultants of New York, New York, New York.

出版信息

Retina. 2017 Nov;37(11):2008-2014. doi: 10.1097/IAE.0000000000001497.

Abstract

PURPOSE

To evaluate the pattern of choriocapillaris signal voids in maternally inherited diabetes and deafness and in pseudoxanthoma elasticum in eyes before the development of any geographic atrophy.

METHODS

The choriocapillaris under the central macula was imaged with the Optovue RTVue XR Avanti using a 10 μm slab thickness. Automatic local thresholding of the resultant raw data extracted areas of absent flow signal, called signal voids, and these were counted and logarithmically binned. The signal void patterns were analyzed in four eyes of two patients with maternally inherited diabetes and deafness and four eyes of three patients with pseudoxanthoma elasticum. None of the patients had geographic atrophy. These data were compared with 55 eyes of 38 healthy control subjects and analyzed with generalized estimating equations.

RESULTS

The choriocapillaris images in maternally inherited diabetes and deafness and pseudoxanthoma elasticum show that the model of signal voids followed a power law distribution, but with a slope and offset much lower than the normal control group, adjusted for age (P < 0.001). The eyes in the disease group were much more likely to have signal voids greater than 40,000 μm.

CONCLUSION

Before the development of any overt geographic atrophy, patients with maternally inherited diabetes and deafness and pseudoxanthoma elasticum show pronounced abnormalities of choriocapillaris flow. Current clinical measures of retinal pigment epithelial health only look for areas of cell death, as in geographic atrophy. It is not possible to determine from current imaging if the choriocapillaris loss precedes potential loss of function of the retinal pigment epithelium, such as secretion of vascular endothelial growth factor.

摘要

目的

评估母系遗传糖尿病伴耳聋患者以及弹性假黄瘤患者在出现任何地图样萎缩之前,脉络膜毛细血管信号缺失的模式。

方法

使用Optovue RTVue XR Avanti对黄斑中心下的脉络膜毛细血管进行成像,层厚为10μm。对所得原始数据进行自动局部阈值处理,提取无血流信号区域(即信号缺失区域),并对其进行计数和对数分组。分析了2例母系遗传糖尿病伴耳聋患者的4只眼以及3例弹性假黄瘤患者的4只眼的信号缺失模式。所有患者均未出现地图样萎缩。将这些数据与38名健康对照者的55只眼进行比较,并使用广义估计方程进行分析。

结果

母系遗传糖尿病伴耳聋患者以及弹性假黄瘤患者的脉络膜毛细血管图像显示,信号缺失模式遵循幂律分布,但经年龄校正后,其斜率和截距远低于正常对照组(P < 0.001)。疾病组的眼睛更有可能出现大于40,000μm的信号缺失。

结论

在出现任何明显的地图样萎缩之前,母系遗传糖尿病伴耳聋患者以及弹性假黄瘤患者的脉络膜毛细血管血流存在明显异常。目前视网膜色素上皮健康的临床测量仅关注细胞死亡区域,如地图样萎缩。从目前的成像中无法确定脉络膜毛细血管的丧失是否先于视网膜色素上皮潜在的功能丧失,如血管内皮生长因子的分泌。

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