Angiographic Characteristics in Mild Familial Exudative Vitreoretinopathy with Genetically Confirmed Autosomal Dominant Inheritance.

IF 4.4 Q1 OPHTHALMOLOGY
Misato Okamoto, Itsuka Matsushita, Tatsuo Nagata, Yoshihisa Fujino, Hiroyuki Kondo
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引用次数: 0

Abstract

Purpose: To determine the ultra-widefield fluorescein angiographic (UWFA) characteristics of patients with mild familial exudative vitreoretinopathy (FEVR) who had been confirmed to have pathogenic variants of the autosomal dominant (AD) genes of FEVR.

Design: Single center, observational case series.

Subjects and controls: Thirty-seven patients with mild FEVR from 27 families who had pathogenic variants of the Norrin/β-catenin genes were studied. The controls consisted of 32 family members who had been confirmed not to carry the pathogenic variants or had heterozygous variants of the autosomal recessive inheritance gene.

Methods: Sixty-four UWFA images from the patients were compared with 60 UWFA images from the controls. The relative length of the temporal retina to the peripheral avascular retina was determined. The cut-off ratio of the relative lengths for a clinically significant avascular retina (csAR) associated with AD-FEVR was determined using the receiver operating characteristic (ROC) curves.

Main outcome measures: The presence or absence of 6 peripheral vascular changes (csAR, V-shaped vascular notch, brushy vascular ends, vascular stain, loop vessels or anastomosis, and capillary telangiectasia) were compared between the patients and the controls.

Results: The csAR was set at > 12% of the length from the ora serrata to the optic disc. The patients with AD-FEVR had more frequent retinal changes than the controls for the V-shaped vascular notch (69% vs. 2%; P < 0.001), brushy vascular ends (78% vs. 3%; P < 0.001), csAR (83% vs. 22%; P < 0.001), and vascular stain (70% vs. 35%, P < 0.001). Loop vessels and/or anastomosis of peripheral vessels were found significantly less frequently in the patients than in the controls (39% vs. 73%; P < 0.001). No significant difference was found for capillary telangiectasia between the 2 groups. The combination of the V-shaped vascular notches, brushy vascular ends, and csAR had a sensitivity of 82.8% and specificity of 98.3%, with the highest ROC curve of 0.9.

Conclusions: The combination of V-shaped vascular notch, brushy vascular ends, and csAR can be used as a biomarker for patients with AD-FEVR who have pathogenic variants of the Norrin/β-catenin genes. These findings will allow more accurate segregation analysis in FEVR families and allow better genetic counseling.

Financial disclosure(s): Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

经遗传学证实为常染色体显性遗传的轻度家族性渗出性玻璃体视网膜病变的血管造影特征。
目的:确定轻度家族性渗出性玻璃体视网膜病变(FEVR)患者的超宽场荧光素血管造影(UWFA)特征,这些患者已被证实具有 FEVR 常染色体显性基因(AD)的致病变异:设计:单中心观察性病例系列:研究对象和对照组:研究了来自 27 个家族的 37 名轻度 FEVR 患者,这些患者的 Norrin/β-catenin 基因存在致病变异。对照组由 32 名家庭成员组成,他们已被证实不携带致病变体或具有常染色体隐性遗传基因的杂合变体:将患者的 64 张 UWFA 图像与对照组的 60 张 UWFA 图像进行比较。测定颞叶视网膜与周围无血管视网膜的相对长度。利用接收器操作特征曲线(ROC)确定与 AD-FEVR 相关的临床显著无血管视网膜(csAR)相对长度的临界比率:比较患者和对照组是否存在六种周围血管变化:csAR、V 形血管切迹、毛刷状血管末端、血管染色、环状血管和/或吻合、毛细血管扩张:csAR的标准是血清口到视盘的长度大于12%。与对照组相比,AD-FEVR 患者视网膜上的 V 形血管切迹变化更为频繁(69% 对 2%,PV 形血管切迹、毛刷状血管末端和 csAR 的组合可作为一种生物标志物,用于检测存在 Norrin/β-catenin 基因致病变异的 AD-FEVR 患者。这些发现将有助于对 FEVR 家系进行更准确的分离分析,并提供更好的遗传咨询。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ophthalmology. Retina
Ophthalmology. Retina Medicine-Ophthalmology
CiteScore
7.80
自引率
6.70%
发文量
274
审稿时长
33 days
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