Characterization of the Retinal Phenotype Using Multimodal Imaging in Novel Compound Heterozygote Variants of CYP2U1

IF 3.2 Q1 OPHTHALMOLOGY Ophthalmology science Pub Date : 2024-09-11 DOI:10.1016/j.xops.2024.100618
Ferenc B. Sallo MD, PhD , Chantal Dysli MD, PhD , Franz Josef Holzer MD , Emmanuelle Ranza MD , Michel Guipponi MD , Stylianos E. Antonarakis MD , Francis L. Munier MD , Alan C. Bird MD , Daniel F. Schorderet MD , Beatrice Rossillion MD , Veronika Vaclavik MD
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Abstract

Purpose

To report the retinal phenotype in 2 patients simulating type 2 macular telangiectasis with new variants in CYP2U1 implicated in hereditary spastic paraplegia type 56 (HSP 56).

Design

Cross sectional case series study.

Participants

Five members of a non-consanguineous family (parents and 3 male children) were investigated.

Methods

All family members underwent a full ophthalmic evaluation and multimodal retinal imaging. Two family members demonstrating retinal anomalies underwent additional OCT angiography, dual wavelength autofluorescence and fluorescence lifetime imaging ophthalmoscopy, kinetic perimetry, fundus-correlated microperimetry, electroretinography, and electro-oculography. Whole-exome sequencing was performed in all 5 family members.

Main Outcome Measures

To characterize the retinal phenotype in affected patients with variants in CYP2U1, using multimodal imaging: dual-wavelength autofluorescence, fluorescence lifetime, OCT angiography.

Results

The 2 siblings with compound heterozygous novel variants c.452C>T; p.(Pro151Leu), c.943C>T; p.(Gln315Ter) in CYP2U1 demonstrated parafoveal loss of retinal transparency and hyperreflectivity to blue light, redistribution of macular pigment to the parafoveal edge, photoreceptor loss, and fluorescence lifetime imaging ophthalmoscopy anomalies: a pattern compatible with that seen in macular telangiectasia type 2 (MacTel). One had manifest neurological abnormalities since early childhood; the second had no neurological abnormalities. Each parent and the third sibling were heterozygous for 1 variant and were neurologically and ophthalmically normal.

Conclusions

These CYP2U1 variants are associated with a retinal phenotype very similar to that otherwise specific for MacTel, suggestive of possible links in the etiology and pathogenesis of these diseases.

Financial Disclosure(s)

The author(s) have no proprietary or commercial interest in any materials discussed in this article.
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利用多模态成像确定 CYP2U1 新型复合杂合子变异体视网膜表型的特征
目的报告 2 例类似 2 型黄斑毛细血管扩张症的患者的视网膜表型,这些患者体内的 CYP2U1 存在新变异,与遗传性痉挛性截瘫 56 型(HSP 56)有关。方法所有家庭成员都接受了全面的眼科评估和多模式视网膜成像。两个视网膜异常的家族成员接受了额外的 OCT 血管造影、双波长自发荧光和荧光寿命成像眼底镜检查、动力性视力测定、眼底相关显微视力测定、视网膜电图和眼底电图检查。主要结果 通过多模态成像:双波长自发荧光、荧光寿命、OCT 血管造影,描述 CYP2U1 变异患者的视网膜表型。C>T;p.(Gln315Ter)的两个兄弟姐妹的视网膜视网膜透明度下降,对蓝光有高反射性,黄斑色素重新分布到视网膜视网膜边缘,感光器缺失,荧光寿命成像眼底镜检查异常:与黄斑毛细血管扩张症 2 型(MacTel)的模式一致。其中一人从幼年起就有明显的神经系统异常,而第二个兄弟姐妹则没有神经系统异常。结论这些CYP2U1变体与MacTel的视网膜表型非常相似,提示这些疾病的病因和发病机制可能存在联系。
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来源期刊
Ophthalmology science
Ophthalmology science Ophthalmology
CiteScore
3.40
自引率
0.00%
发文量
0
审稿时长
89 days
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