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早期特发性黄斑毛细血管扩张症中黄斑中心凹视锥细胞密度降低

Reduced foveal cone density in early idiopathic macular telangiectasia.

作者信息

Song Hongxin, Rossi Ethan A, Williams David R

机构信息

Beijing Tongren Eye Center, Beijing Institute of Ophthalmology, Beijing Tongren Hospital, Capital Medical University, Beijing, China.

Department of Ophthalmology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

出版信息

BMJ Open Ophthalmol. 2021 Jan 8;6(1):e000603. doi: 10.1136/bmjophth-2020-000603. eCollection 2021.

Abstract

OBJECTIVE

Idiopathic macular telangiectasia (MacTel) is considered primarily a vascular disease affecting juxtafoveal retinal capillaries. However, recent evidence suggests that neuronal changes may occur early in disease development. We used high-resolution adaptive optics retinal imaging to elucidate the foveal cone photoreceptor changes at a cellular level in patients with MacTel.

METHODS AND ANALYSIS

We used adaptive optics scanning light ophthalmoscopy (AOSLO) to evaluate the foveal cone photoreceptors in the less-affected eye of patients with asymmetric MacTel. AOSLO images of cone photoreceptors were obtained in a 4°×4° area centred on the foveola. Individual cone positions were identified within a 2°×2° area centred on the fovea, using semiautomatic cone marking software with manual correction, permitting calculation of a map of cone density.

RESULTS

In all participants, one eye was affected with MacTel, the fellow eye was clinically normal or near normal, with visual acuity of 20/25 or better and subtle angiographic leakage. The foveal cone mosaics were continuous with tight packing and cones exhibited normal reflectivity. However, cone density was significantly lower for all participants (mean=80 733 cones/mm) within 0.5° than the cone density previously reported for normal eyes.

CONCLUSIONS

Foveal cone density is lower than normal in the clinically less-affected eyes of patients with asymmetric MacTel. This suggests that cone photoreceptor loss may precede classic obvious vascular changes in idiopathic MacTel.

摘要

目的

特发性黄斑毛细血管扩张症(MacTel)主要被认为是一种影响黄斑旁视网膜毛细血管的血管疾病。然而,最近的证据表明,神经元变化可能在疾病发展早期就会出现。我们使用高分辨率自适应光学视网膜成像技术,在细胞水平上阐明MacTel患者的中央凹视锥光感受器变化。

方法与分析

我们使用自适应光学扫描激光检眼镜(AOSLO)评估不对称性MacTel患者患侧症状较轻眼睛的中央凹视锥光感受器。在以中央凹为中心的4°×4°区域内获取视锥光感受器的AOSLO图像。使用半自动视锥标记软件并进行手动校正,在以中央凹为中心的2°×2°区域内确定单个视锥的位置,从而计算视锥密度图。

结果

所有参与者中,一只眼睛患有MacTel,另一只眼睛临床正常或接近正常,视力为20/25或更好,且血管造影有轻微渗漏。中央凹视锥镶嵌结构连续,排列紧密,视锥表现出正常的反射率。然而,所有参与者在0.5°范围内的视锥密度(平均=80733个视锥/mm)显著低于先前报道的正常眼睛的视锥密度。

结论

在不对称性MacTel患者临床症状较轻的眼睛中,中央凹视锥密度低于正常水平。这表明在特发性MacTel中,视锥光感受器的丧失可能先于典型的明显血管变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e8c/7798656/a211d9ceac66/bmjophth-2020-000603f01.jpg

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