The longitudinal progression of MRI changes in pre-ataxic carriers of SCA3/MJD

被引:6
作者
de Oliveira, Camila Maria [1 ,2 ]
Leotti, Vanessa Bielefeldt [3 ,4 ]
Polita, Sandra [5 ]
Anes, Mauricio [6 ]
Cappelli, Amanda Henz [7 ]
Rocha, Anastacia Guimaraes [7 ]
Ecco, Gabriela [7 ]
Bolzan, Gabriela [2 ,8 ]
Kersting, Nathalia [1 ,2 ]
Duarte, Juliana Avila [1 ,5 ,7 ]
Saraiva-Pereira, Maria-Luiza [2 ,8 ,9 ,10 ]
Franca Junior, Marcondes Cavalcante [11 ,13 ]
Rezende, Thiago Junqueira Ribeiro [11 ,13 ,14 ]
Jardim, Laura Bannach [1 ,2 ,7 ,8 ,9 ,12 ,14 ]
机构
[1] Univ Fed Rio Grande do Sul, Programa Posgrad Ciencias Med, Porto Alegre, Brazil
[2] Hosp Clin Porto Alegre, Ctr Pesquisa Clin & Expt, Porto Alegre, Brazil
[3] Univ Fed Rio Grande do Sul, Dept Estat, Porto Alegre, Brazil
[4] Univ Fed Rio Grande do Sul, Programa Posgrad Epidemiol, Porto Alegre, Brazil
[5] Hosp Clin Porto Alegre, Serv Radiol, Porto Alegre, Brazil
[6] Hosp Clin Porto Alegre, Serv Fis Med & Radioprotecao, Porto Alegre, Brazil
[7] Univ Fed Rio Grande do Sul, Fac Med, Porto Alegre, Brazil
[8] Univ Fed Rio Grande do Sul, Programa Posgrad Genet & Biol Mol, Porto Alegre, Brazil
[9] Hosp Clin Porto Alegre, Serv Genet Med, Porto Alegre, Brazil
[10] Univ Fed Rio Grande do Sul, Dept Bioquim, Porto Alegre, Brazil
[11] Univ Estadual Campinas UNICAMP, Fac Ciencias Med, Dept Neurol, Campinas, Brazil
[12] Univ Fed Rio Grande do Sul, Dept Med Interna, Porto Alegre, Brazil
[13] Neuroimaging Lab, Rua Vital Brasil 89-99, BR-13083888 Campinas, SP, Brazil
[14] Hosp Clin Porto Alegre, Med Genet Serv, Rua Ramiro Barcelos 2350, BR-90035003 Porto Alegre, Brazil
关键词
Biomarkers; Pre-ataxic period; Spinocerebellar ataxia type 3; MRI; DTI; MACHADO-JOSEPH-DISEASE; SPINOCEREBELLAR; SEVERITY; ATROPHY; SCALE; SCORE;
D O I
10.1007/s00415-023-11763-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundThe natural history of magnetic resonance imaging (MRI) in pre-ataxic stages of spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD) is not well known. We report cross-sectional and longitudinal data obtained at this stage.MethodsBaseline (follow-up) observations included 32 (17) pre-ataxic carriers (SARA < 3) and 20 (12) related controls. The mutation length was used to estimate the time to onset (TimeTo) of gait ataxia. Clinical scales and MRIs were performed at baseline and after a median (IQR) of 30 (7) months. Cerebellar volumetries (ACAPULCO), deep gray-matter (T1-Multiatlas), cortical thickness (FreeSurfer), cervical spinal cord area (SCT) and white matter (DTI-Multiatlas) were assessed. Baseline differences between groups were described; variables that presented a p < 0.1 after Bonferroni correction were assessed longitudinally, using TimeTo and study time. For TimeTo strategy, corrections for age, sex and intracranial volume were done with Z-score progression. A significance level of 5% was adopted.ResultsSCT at C1 level distinguished pre-ataxic carriers from controls. DTI measures of the right inferior cerebellar peduncle (ICP), bilateral middle cerebellar peduncles (MCP) and bilateral medial lemniscus (ML), also distinguished pre-ataxic carriers from controls, and progressed over TimeTo, with effect sizes varying from 0.11 to 0.20, larger than those of the clinical scales. No MRI variable showed progression over study time.DiscussionDTI parameters of the right ICP, left MCP and right ML were the best biomarkers for the pre-ataxic stage of SCA3/MJD. TimeTo is an interesting timescale, since it captured the longitudinal worsening of these structures.
引用
收藏
页码:4276 / 4287
页数:12
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