A Phenotypic Study of CRB1 Retinopathy Secondary to the Variant p.(Pro836Thr) Prevalent in Those of Black African Ancestry.

IF 5 2区 医学 Q1 OPHTHALMOLOGY
Wendy M Wong, Anthony G Robson, Rebecca A Baker, Gavin Arno, Joseph Van Aerschot, Siying Lin, Mariya Moosajee, Michel Michaelides, Omar A Mahroo, Andrew R Webster
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Abstract

Purpose: To comprehensively characterize the clinical consequences of the CRB1 variant p.(Pro836Thr). In African populations, this variant has an allele frequency of 0.329% (gnomAD v4.1.0).

Methods: This study was a retrospective case series of 14 patients from 11 families with molecularly confirmed CRB1-associated retinal dystrophy, each possessing at least one p.(Pro836Thr) variant. The age at onset of visual symptoms, best-corrected visual acuity, imaging findings, and quantitative electrophysiologic measurements of retinal function were analyzed.

Results: The p.(Pro836Thr) variant was homozygous in four families and compound heterozygous in seven families. The familial origins included Nigeria (n = 4), Ghana (n = 3), the Caribbean region (n = 2), and Uganda (n = 1). The median follow-up was 7 years (interquartile range, 3-16). Symptom onset was most common in childhood (eight patients, 57.1%). Reduced central vision was the most frequent presenting symptom (12 patients, 85%). Widefield multimodal imaging revealed peripheral retinal changes in addition to macular changes in three patients. Nine patients had international standard electrophysiology and showed generalized retinal dysfunction with a similar degree of rod and cone system involvement (n = 7) or a clear rod-cone pattern of dysfunction (n = 2). All had pattern electroretinography (ERG) evidence of macular dysfunction.

Conclusions: The study highlights the association of the p.(Pro836Thr) variant with African ancestry and characterizes their key clinical and electrophysiological features. Our study suggests that the p.(Pro836Thr) variant confers a less severe consequence on retinal function and structure than the majority of other reported CRB1 variants. Although retinal imaging may show alterations confined to the macular region, electrophysiology in this series indicates generalized cone and rod photoreceptor dysfunction.

在非洲黑人祖先中流行的变异p.(Pro836Thr)继发的CRB1视网膜病变的表型研究
目的:全面表征CRB1变异p.(Pro836Thr)的临床后果。在非洲人群中,该变异的等位基因频率为0.329% (gnomAD v4.1.0)。方法:本研究回顾性分析了来自11个家族的14例经分子证实的crb1相关视网膜营养不良患者,每位患者至少具有一个p.(Pro836Thr)变体。分析了视力症状的发病年龄、最佳矫正视力、影像学表现和视网膜功能的定量电生理测量。结果:p.(Pro836Thr)变异在4个家族中为纯合子,在7个家族中为复合杂合子。家族起源包括尼日利亚(n = 4)、加纳(n = 3)、加勒比地区(n = 2)和乌干达(n = 1)。中位随访时间为7年(四分位数间距3-16)。儿童期发病最常见(8例,57.1%)。中心视力下降是最常见的症状(12例,85%)。广角多模态成像显示除了黄斑病变外,还有视网膜周围病变。9例患者具有国际标准的电生理,表现出全身性视网膜功能障碍,伴有类似程度的视杆和视锥系统受累(n = 7)或明显的视杆-视锥模式功能障碍(n = 2)。所有患者均有视网膜电图(ERG)模式黄斑功能障碍的证据。结论:该研究强调了p.(Pro836Thr)变异与非洲血统的关联,并表征了其关键的临床和电生理特征。我们的研究表明,p.(Pro836Thr)变异对视网膜功能和结构的影响比大多数其他已报道的CRB1变异要小。虽然视网膜成像可能显示局限于黄斑区域的改变,但本系列的电生理学显示广泛的视锥和视杆光感受器功能障碍。
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来源期刊
CiteScore
6.90
自引率
4.50%
发文量
339
审稿时长
1 months
期刊介绍: Investigative Ophthalmology & Visual Science (IOVS), published as ready online, is a peer-reviewed academic journal of the Association for Research in Vision and Ophthalmology (ARVO). IOVS features original research, mostly pertaining to clinical and laboratory ophthalmology and vision research in general.
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