Lima Manuela, Raposo Mafalda, Ferreira Ana, Melo Ana Rosa Vieira, Pavão Sara, Medeiros Filipa, Teves Luís, Gonzalez Carlos, Lemos João, Pires Paula, Lopes Pedro, Valverde David, Gonzalez José, Kay Teresa, Vasconcelos João
Faculdade de Ciências e Tecnologia, Universidade dos Açores, 9500-321 Ponta Delgada, Portugal.
Instituto de Biologia Molecular e Celular (IBMC), Universidade do Porto, 4200-135 Porto, Portugal.
Biomedicines. 2023 Jan 18;11(2):247. doi: 10.3390/biomedicines11020247.
Machado-Joseph disease (MJD)/spinocerebellar ataxia type 3 (SCA3) is the most common autosomal dominant ataxia worldwide. MJD is characterized by late-onset progressive cerebellar ataxia associated with variable clinical findings, including pyramidal signs and a dystonic-rigid extrapyramidal syndrome. In the Portuguese archipelago of the Azores, the worldwide population cluster for this disorder (prevalence of 39 in 100,000 inhabitants), a cohort of MJD mutation carriers belonging to extensively studied pedigrees has been followed since the late 1990s. Studies of the homogeneous Azorean MJD cohort have been contributing crucial information to the natural history of this disease as well as allowing the identification of novel molecular biomarkers. Moreover, as interventional studies for this globally rare and yet untreatable disease are emerging, this cohort should be even more important for the recruitment of trial participants. In this paper, we profile the Azorean cohort of MJD carriers, constituted at baseline by 20 pre-ataxic carriers and 52 patients, which currently integrates the European spinocerebellar ataxia type 3/Machado-Joseph disease Initiative (ESMI), a large European longitudinal MJD cohort. Moreover, we summarize the main studies based on this cohort and highlight the contributions made to advances in MJD research. Knowledge of the profile of the Azorean MJD cohort is not only important in the context of emergent interventional trials but is also pertinent for the implementation of adequate interventional measures, constituting relevant information for Lay Associations and providing data to guide healthcare decision makers.
马查多-约瑟夫病(MJD)/3型脊髓小脑共济失调(SCA3)是全球最常见的常染色体显性共济失调。MJD的特征是迟发性进行性小脑共济失调,并伴有多种临床症状,包括锥体束征和肌张力障碍-僵硬的锥体外系综合征。在亚速尔群岛的葡萄牙群岛,是这种疾病在全球的人群聚集区(每10万居民中有39例患病率),自20世纪90年代末以来,对一群属于经过广泛研究的家系的MJD突变携带者进行了跟踪研究。对亚速尔群岛MJD同质性队列的研究为这种疾病的自然史提供了关键信息,也有助于识别新的分子生物标志物。此外,随着针对这种全球罕见且无法治疗的疾病的干预性研究不断涌现,这个队列对于招募试验参与者来说将变得更加重要。在本文中,我们介绍了MJD携带者的亚速尔群岛队列,该队列在基线时由20名共济失调前期携带者和52名患者组成,目前已纳入欧洲3型脊髓小脑共济失调/马查多-约瑟夫病倡议(ESMI),这是一个大型的欧洲MJD纵向队列。此外,我们总结了基于该队列的主要研究,并强调了对MJD研究进展所做出的贡献。了解亚速尔群岛MJD队列的情况不仅在新兴的干预性试验背景下很重要,而且对于实施适当的干预措施也很相关,为患者协会提供了相关信息,并为指导医疗保健决策者提供了数据。