The role of multimodal imaging and vision function testing in ABCA4-related retinopathies and their relevance to future therapeutic interventions.

IF 2.3 Q2 OPHTHALMOLOGY
Therapeutic Advances in Ophthalmology Pub Date : 2021-12-19 eCollection Date: 2021-01-01 DOI:10.1177/25158414211056384
Saoud Al-Khuzaei, Mital Shah, Charlotte R Foster, Jing Yu, Suzanne Broadgate, Stephanie Halford, Susan M Downes
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引用次数: 4

Abstract

The aim of this review article is to describe the specific features of Stargardt disease and ABCA4 retinopathies (ABCA4R) using multimodal imaging and functional testing and to highlight their relevance to potential therapeutic interventions. Standardised measures of tissue loss, tissue function and rate of change over time using formal structured deep phenotyping in Stargardt disease and ABCA4R are key in diagnosis, and prognosis as well as when selecting cohorts for therapeutic intervention. In addition, a meticulous documentation of natural history will be invaluable in the future to compare treated with untreated retinas. Despite the familiarity with the term Stargardt disease, this eponymous classification alone is unhelpful when evaluating ABCA4R, as the ABCA4 gene is associated with a number of phenotypes, and a range of severity. Multimodal imaging, psychophysical and electrophysiologic measurements are necessary in diagnosing and characterising these differing retinopathies. A wide range of retinal dystrophy phenotypes are seen in association with ABCA4 mutations. In this article, these will be referred to as ABCA4R. These different phenotypes and the existence of phenocopies present a significant challenge to the clinician. Careful phenotypic characterisation coupled with the genotype enables the clinician to provide an accurate diagnosis, associated inheritance pattern and information regarding prognosis and management. This is particularly relevant now for recruiting to therapeutic trials, and in the future when therapies become available. The importance of accurate genotype-phenotype correlation studies cannot be overemphasised. This approach together with segregation studies can be vital in the identification of causal mutations when variants in more than one gene are being considered as possible. In this article, we give an overview of the current imaging, psychophysical and electrophysiological investigations, as well as current therapeutic research trials for retinopathies associated with the ABCA4 gene.

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多模态成像和视觉功能测试在abca4相关视网膜病变中的作用及其与未来治疗干预的相关性
这篇综述文章的目的是利用多模态成像和功能测试来描述Stargardt病和ABCA4视网膜病变(ABCA4R)的具体特征,并强调它们与潜在治疗干预措施的相关性。在Stargardt病和ABCA4R中使用正式的结构化深度表型对组织损失、组织功能和随时间变化的速率进行标准化测量是诊断、预后以及选择治疗干预队列的关键。此外,一份细致的自然历史文献在将来比较治疗和未治疗的视网膜时将是无价的。尽管我们熟悉Stargardt病这一术语,但在评估ABCA4R时,这种单独的同名分类是没有帮助的,因为ABCA4基因与许多表型和一系列严重程度相关。多模态成像,心理物理和电生理测量是诊断和表征这些不同视网膜病变所必需的。广泛的视网膜营养不良表型与ABCA4突变有关。在本文中,这些将被称为ABCA4R。这些不同的表型和表型的存在对临床医生提出了重大挑战。仔细的表型特征与基因型相结合,使临床医生能够提供准确的诊断、相关的遗传模式以及有关预后和管理的信息。这对于现在的治疗试验招募,以及将来有治疗方法可用时,都是特别重要的。准确的基因型-表型相关研究的重要性再怎么强调也不为过。当一个以上的基因变异被认为是可能的时候,这种方法和分离研究对于确定因果突变是至关重要的。在这篇文章中,我们概述了目前与ABCA4基因相关的视网膜病变的成像、心理物理和电生理研究,以及目前的治疗研究试验。
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
CiteScore
4.50
自引率
0.00%
发文量
44
审稿时长
12 weeks
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