眼球震颤的新疗法:到目前为止,遗传学教会了我们什么?

Therapeutic advances in rare disease Pub Date : 2021-03-23 eCollection Date: 2021-01-01 DOI:10.1177/2633004021998714
Jay E Self, Helena Lee
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引用次数: 1

摘要

眼球震颤是一种以眼睛不受控制、重复、来回运动为特征的疾病。它可以作为一种看似孤立的疾病发生,但最常见的是一系列眼科和系统性疾病的第一个或最明显的特征。潜在原因的数量是巨大的,最近在提供基因检测方面的改进表明,许多疾病可能包括眼球震颤,但表型明显重叠。因此,对眼球震颤遗传原因的了解增加表明,成功的“眼球震颤”新疗法可以针对特定的潜在疾病和机制(旨在治疗整个潜在疾病),或最终的共同途径(旨在直接治疗眼球震颤)。简明语言总结:眼球运动障碍(眼球震颤)的新治疗方法:到目前为止,遗传学教会了我们什么?眼球震颤是一种眼球运动障碍,其特征是不受控制的来回运动。它可以作为一种孤立的疾病发生,在影响眼睛其他部位的情况下,在影响身体多个其他部位的条件下,或继发于神经系统疾病(脑部疾病)。近年来,基因检测方法的进步和医疗系统中基因检测的增加,使人们对眼球震颤的根本原因有了更多的了解。他们强调了令人困惑的基因原因,这些原因可能导致看起来非常相似的眼球运动障碍。近年来,针对眼球震颤的一些原因开发了新的药物类别,也针对其他有可能治疗某些类型眼球震颤的疾病开发了一些新药。出于这些原因,遗传学告诉我们,确定新的可能治疗眼震的方法可以取决于确定潜在的遗传原因并致力于治疗,也可以通过靶向最终的共同途径来治疗眼震本身。基于特定条件的特定治疗方法的工具包比基于“一刀切”方法的万灵药更能对“眼球震颤”产生有意义的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Novel therapeutics in nystagmus: what has the genetics taught us so far?

Novel therapeutics in nystagmus: what has the genetics taught us so far?

Nystagmus is a disorder characterised by uncontrolled, repetitive, to-and-fro movement of the eyes. It can occur as a seemingly isolated disorder but is most commonly the first, or most obvious, feature in a host of ophthalmic and systemic disorders. The number of underlying causes is vast, and recent improvements in the provision of genetic testing have shown that many conditions can include nystagmus as a feature, but that phenotypes overlap significantly. Therefore, an increase in the understanding of the genetic causes of nystagmus has shown that successful novel therapeutics for 'nystagmus' can target either specific underlying disorders and mechanisms (aiming to treat the underlying condition as a whole), or a final common pathway (aiming to treat the nystagmus directly).

Plain language summary: Novel treatments for a disorder of eye movement (nystagmus): what has the genetics taught us so far? Nystagmus is a disorder of eye movement characterised by uncontrolled, to-and-fro movements. It can occur as an isolated disorder, in conditions affecting other parts of the eye, in conditions affecting multiple other parts of the body or secondary to neurological diseases (brain diseases). In recent years, advances in genetic testing methods and increase in genetic testing in healthcare systems have provided a greater understanding of the underlying causes of nystagmus. They have highlighted the bewildering number of genetic causes that can result in what looks like a very similar eye movement disorder.In recent years, new classes of drugs have been developed for some of the causes of nystagmus, and some new drugs have been developed for other conditions which have the potential to work in certain types of nystagmus. For these reasons, genetics has taught us that identifying new possible treatments for nystagmus can either be dependent on identifying the underlying genetic cause and aiming to treat that, or aiming to treat the nystagmus per se by targeting a final common pathway. A toolkit based on specific treatments for specific conditions is more to have meaningful impact on 'nystagmus' than pursuing a panacea based on a 'one size fits all' approach.

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