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早发性遗传性肌张力障碍与晚发性特发性肌张力障碍:相同或不同的生物学机制?

Early-onset inherited dystonias versus late-onset idiopathic dystonias: Same or different biological mechanisms?

机构信息

Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Baronissi, SA, Italy.

Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy; Dino Ferrari Center, Neuroscience Section, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.

出版信息

Int Rev Neurobiol. 2023;169:329-346. doi: 10.1016/bs.irn.2023.05.002. Epub 2023 Jun 27.

Abstract

Dystonia syndromes encompass a heterogeneous group of movement disorders which might be differentiated by several clinical-historical features. Among the latter, age-at-onset is probably the most important in predicting the likelihood both for the symptoms to spread from focal to generalized and for a genetic cause to be found. Accordingly, dystonia syndromes are generally stratified into early-onset and late-onset forms, the former having a greater likelihood of being monogenic disorders and the latter to be possibly multifactorial diseases, despite being currently labeled as idiopathic. Nonetheless, there are several similarities between these two groups of dystonia, including shared pathophysiological and biological mechanisms. Moreover, there is also initial evidence of age-related modifiers of early-onset dystonia syndromes and of critical periods of vulnerability of the sensorimotor network, during which a combination of genetic and non-genetic insults is more likely to produce symptoms. Based on these lines of evidence, we reappraise the double-hit hypothesis of dystonia, which would accommodate both similarities and differences between early-onset and late-onset dystonia in a single framework.

摘要

肌张力障碍综合征包括一组异质性运动障碍,其可能通过多种临床-历史特征来区分。在这些特征中,发病年龄可能是预测症状从局灶性向全身性扩散以及是否存在遗传原因的最重要因素。因此,肌张力障碍综合征通常分为早发型和晚发型,前者更有可能是单基因疾病,后者则可能是多因素疾病,尽管目前被标记为特发性。然而,这两种类型的肌张力障碍之间存在许多相似之处,包括共同的病理生理和生物学机制。此外,也有初步证据表明早发型肌张力障碍综合征存在与年龄相关的修饰因子,以及感觉运动网络的易损性关键期,在此期间,遗传和非遗传因素的组合更有可能产生症状。基于这些证据,我们重新评估了肌张力障碍的双重打击假说,该假说可以在一个框架内同时包含早发型和晚发型肌张力障碍的相似性和差异。

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