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伏格特-小柳-原田病中黄斑视锥光感受器的恢复

Recovery of macular cone photoreceptors in Vogt-Koyanagi-Harada disease.

作者信息

Nakamura Tomoko, Hayashi Atsushi, Oiwake Toshihiko

机构信息

Department of Ophthalmology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.

出版信息

Graefes Arch Clin Exp Ophthalmol. 2018 Feb;256(2):387-394. doi: 10.1007/s00417-017-3869-5. Epub 2017 Dec 20.

Abstract

PURPOSE

Our purpose was to study changes in macular cone photoreceptors in Vogt-Koyanagi-Harada (VKH) disease patients after high-dose corticosteroid treatment using an adaptive optics (AO) fundus camera.

METHODS

We retrospectively analyzed 16 eyes of eight patients with new-onset acute VKH disease that were studied retrospectively. After serous retinal detachment (SRD) had resolved, AO images were obtained using the rtx1™ AO fundus camera over a 12-month course. Cone counting was performed in the nasal, temporal, superior and inferior areas of the macula 0.75 mm from the foveal center. A control group of 30 eyes of 30 healthy subjects was established for comparison.

RESULTS

In the eyes with VKH disease, the mean cone densities 0.75 mm from the foveal center were 11,847 at baseline (resolution of SRD), and 15,218, 16,684 and 17,686 cones/mm, at 3, 6, and 12 months later, respectively. The mean cone densities at 3, 6, and 12 months were significantly increased compared to those of baseline (p = 0.007, p < 0.001, and p < 0.001, respectively); however, they were significantly lower than that of the healthy control eyes (p < 0.001). The mean cone densities at areas with a previous presence of cystoid spaces were significantly lower than those without cystoid spaces at the baseline, and at 3, 6, and 12 months (p < 0.001, p = 0.007, p < 0.001, and p = 0.008, respectively).

CONCLUSIONS

Cone densities were gradually increased after the resolution of SRD in the eyes of VKH disease patients. The presence of cystoid spaces might be a marker of severe damage to cone photoreceptors.

摘要

目的

我们的目的是使用自适应光学(AO)眼底相机研究大剂量皮质类固醇治疗后Vogt-小柳-原田(VKH)病患者黄斑区视锥光感受器的变化。

方法

我们回顾性分析了8例新发急性VKH病患者的16只眼睛。浆液性视网膜脱离(SRD)消退后,使用rtx1™AO眼底相机在12个月的病程中获取AO图像。在距黄斑中心凹0.75毫米的黄斑鼻侧、颞侧、上方和下方区域进行视锥细胞计数。建立了一个由30名健康受试者的30只眼睛组成的对照组进行比较。

结果

在患有VKH病的眼睛中,距黄斑中心凹0.75毫米处的平均视锥细胞密度在基线时(SRD消退时)为11,847个,在3、6和12个月后分别为15,218、16,684和17,686个视锥细胞/平方毫米。与基线相比,3、6和12个月时的平均视锥细胞密度显著增加(分别为p = 0.007、p < 0.001和p < 0.001);然而,它们显著低于健康对照眼睛(p < 0.001)。在基线时以及3、6和12个月时,先前存在囊样间隙区域的平均视锥细胞密度显著低于无囊样间隙区域(分别为p < 0.001、p = 0.007、p < 0.001和p = 0.008)。

结论

VKH病患者眼睛的SRD消退后,视锥细胞密度逐渐增加。囊样间隙的存在可能是视锥光感受器严重损伤的一个标志。

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