Department of Ophthalmology, St. Franziskus Hospital, Münster, Germany.
Retinal Disorders and Ophthalmic Genetics, Jules Stein Eye Institute, Los Angeles, California, USA.
Br J Ophthalmol. 2021 Apr;105(4):573-576. doi: 10.1136/bjophthalmol-2020-317997. Epub 2021 Jan 7.
Macular telangiectasia type 2 (MacTel) is a neurodegenerative disease resulting in photoreceptor loss. Optical coherence tomography (OCT) reveals outer retina-associated hyperreflectivity (ORaH) as part of this process. The purpose of this study was to describe the incidence and phenotypical variation of ORaH.
Different parameters of ORaH were analysed: OCT characteristics (Spectralis SD-OCT), correlation with vascular changes (OCT angiography; OCTA 3×3 mm Optovue) and correlation with hyperpigmentation (autofluorescence/fundus images). ORaH was also evaluated regarding the grade of severity of photoreceptor loss (Disease Severity Scale).
Of 220 eyes with MacTel type 2, 106 demonstrated ORaH. On OCT, the size, the extension into the inner retina and the contact with retinal pigment epithelium (RPE) of the ORaH were variable. On OCTA neovascularisation (NV) in the outer retina (OR) was present at the location of the ORaH in 97.6%. Increasing size of NV correlated with progressive photoreceptor loss. In 86.6% with NV, the flow signals were visible between the OR and the choriocapillaris. In 85.7%, the ORaH was associated with hyperpigmentation on autofluorescence and fundus colour images.
The presence of ORaH is associated with increasing photoreceptor loss and disease severity. In these more advanced cases of the present study, a variable presentation of ORaH in respect to size and form was seen, but in most cases, ORaH was in contact to the RPE. Additionally, ORaH was associated with hyperpigmentation and OR NV on OCTA. These results are consistent with the concept of ORaH representing fibrovascular OR-NV with RPE proliferation after contact with the RPE.
黄斑毛细血管扩张症 2 型(MacTel)是一种导致光感受器损失的神经退行性疾病。光学相干断层扫描(OCT)显示外视网膜相关高反射性(ORaH)是该过程的一部分。本研究的目的是描述 ORaH 的发生率和表型变化。
分析了 ORaH 的不同参数:OCT 特征(Spectralis SD-OCT)、与血管变化的相关性(OCT 血管造影;OCTA 3×3mm Optovue)以及与高色素沉着的相关性(自发荧光/眼底图像)。还根据光感受器损失的严重程度(疾病严重程度量表)评估了 ORaH。
在 220 只 MacTel 2 型眼中,有 106 只出现了 ORaH。在 OCT 上,ORaH 的大小、向视网膜内延伸的程度以及与视网膜色素上皮(RPE)的接触情况各不相同。在 OCTA 上,在外视网膜(OR)中存在新生血管(NV)的位置,在 97.6%的病例中存在 ORaH。NV 大小的增加与光感受器损失的进行性增加相关。在 86.6%的存在 NV 的病例中,可见 OR 和脉络膜毛细血管之间的血流信号。在 85.7%的病例中,ORaH与自发荧光和眼底彩色图像上的高色素沉着相关。
ORaH 的存在与光感受器损失的增加和疾病严重程度相关。在本研究的这些更晚期病例中,ORaH 在大小和形态上表现出不同的特征,但在大多数情况下,ORaH 与 RPE 接触。此外,ORaH 与 OCTA 上的 OR 高反射和 OR NV 相关。这些结果与 ORaH 代表与 RPE 接触后的纤维血管 OR-NV 和 RPE 增殖的概念一致。