Structural brain and spinal cord damage in symptomatic and pre-symptomatic VAPB-related ALS

被引:7
作者
Tauana, B. Leoni [1 ]
Rezende, Thiago Junqueira R. [1 ]
Peluzzo, Thiago M. [2 ]
Martins, Melina P. [1 ]
Neto, Antonio Rodrigues Coimbra [1 ]
Gonzalez-Salazar, Carelis [1 ]
Cruzeiro, Marcelo Maroco [3 ]
Camargos, Sarah Teixeira [4 ]
de Souza, Leonardo Cruz [4 ]
Franca, Marcondes C., Jr. [1 ]
机构
[1] Univ Campinas UNICAMP, Sch Med Sci, Dept Neurol, Campinas, SP, Brazil
[2] Univ Campinas UNICAMP, Sch Med Sci, Dept Med Genet, Campinas, SP, Brazil
[3] Fed Univ Juiz de Fora UFJF, Dept Internal Med, Juiz De Fora, MG, Brazil
[4] Fed Univ Minas Gerais UFMG, Sch Med, Dept Internal Med, Belo Horizonte, MG, Brazil
基金
巴西圣保罗研究基金会;
关键词
Amyotrophic lateral sclerosis; VAPB; Genetics; MRI; Presymptomatic; AMYOTROPHIC-LATERAL-SCLEROSIS; HUMAN CEREBRAL-CORTEX; PROTEIN VAPB; MUTATION; DISEASE; SEGMENTATION; ATROPHY; ATLAS;
D O I
10.1016/j.jns.2021.120126
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: The VAPB gene is associated with fALS (fALS 8). This disease presents a variable phenotype and no study sought to characterize its neuroanatomical abnormalities until now. This study aims to evaluate structural brain and spinal cord abnormalities in symptomatic and pre-symptomatic VAPB-related ALS.Methods: This cohort included 10 presymptomatic and 20 symptomatic carriers of the Pro56Ser VAPB variant as well as 30 matched controls and 20 individuals with sporadic ALS. They underwent detailed clinical evaluation and MRI in a 3 T scanner. Using volumetric T1 sequence, we computed cerebral cortical thickness (FreeSurfer), basal ganglia volumetry (T1 Multi-atlas) and SC morphometry (SpineSeg). DTI was used to assess white matter integrity (DTI Multi-atlas). Groups were compared using a generalized linear model with Bonferroni-corrected p values<0.05. We also plotted VAPB brain expression map using Allen Human Brain Atlas to compare with imaging findings.Results: Mean age of presymptomatic and symptomatic subjects were 43.2 and 51.9 years, respectively. Most patients had a predominant lower motor neuron phenotype (16/20). Sleep complaints and tremor were the most frequent additional manifestations. Compared to controls, symptomatic subjects had pallidal, brainstem and SC atrophy, whereas presymptomatic only had SC atrophy. This pattern also contrasted with the sALS group that presented motor cortex and corticospinal abnormalities. Brain structural damage and VAPB expression maps were highly overlapping.Conclusion: VAPB-related ALS has a distinctive structural signature that targets the basal ganglia, brainstem and SC, which are regions with high VAPB expression. Neuroanatomical SC changes are evident before clinical onset of the disease.
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页数:6
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