Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Pearse Street, Dublin 2, Ireland.
Electronics and Computer Science, University of Southampton, Southampton, UK.
Brain Imaging Behav. 2021 Oct;15(5):2283-2296. doi: 10.1007/s11682-020-00421-4. Epub 2021 Jan 7.
Primary lateral sclerosis (PLS) is classically considered a 'pure' upper motor neuron disorder. Motor cortex atrophy and pyramidal tract degeneration are thought to be pathognomonic of PLS, but extra-motor cerebral changes are poorly characterized. In a prospective neuroimaging study, forty PLS patients were systematically evaluated with a standardised imaging, genetic and clinical protocol. Patients were screened for ALS and HSP associated mutations, as well as C9orf72 hexanucleotide repeats. Clinical assessment included composite reflex scores, spasticity scales, functional rating scales, and screening for cognitive and behavioural deficits. The neuroimaging protocol evaluated cortical atrophy patterns, subcortical grey matter changes and white matter alterations in whole-brain and region-of-interest analyses. PLS patients tested negative for known ALS- and HSP-associated mutations and C9orf72 repeat expansions. Voxel-wise analyses revealed anterior cingulate, dorsolateral prefrontal, insular, opercular, orbitofrontal and bilateral mesial temporal grey matter changes and white matter alterations in the fornix, brainstem, temporal lobes, and cerebellum. Significant thalamus, caudate, hippocampus, putamen and accumbens nucleus volume reductions were also identified. Extra-motor clinical manifestations were dominated by verbal fluency deficits, language deficits, apathy and pseudobulbar affect. Our clinical and radiological evaluation confirms considerable extra-motor changes in a population-based cohort of PLS patients. Our data suggest that PLS should no longer be considered a neurodegenerative disorder selectively affecting the pyramidal system. PLS is associated with widespread extra-motor changes and manifestations which should be carefully considered in the multidisciplinary management of this low-incidence condition.
原发性侧索硬化症(PLS)通常被认为是一种“纯”上运动神经元疾病。运动皮层萎缩和皮质脊髓束变性被认为是 PLS 的特征性改变,但对其以外的脑部改变的特征描述较差。在一项前瞻性神经影像学研究中,对 40 例 PLS 患者进行了标准影像学、遗传学和临床方案的系统评估。对患者进行了 ALS 和 HSP 相关突变以及 C9orf72 六核苷酸重复的筛查。临床评估包括复合反射评分、痉挛量表、功能评定量表以及认知和行为缺陷的筛查。神经影像学方案评估了全脑和感兴趣区分析中的皮质萎缩模式、皮质下灰质变化和白质改变。PLS 患者的已知 ALS 和 HSP 相关突变以及 C9orf72 重复扩增检测均为阴性。体素分析显示,前扣带回、背外侧前额叶、岛叶、脑岛盖部、眶额部和双侧内侧颞叶灰质发生变化,穹窿、脑干、颞叶和小脑的白质也发生改变。还发现丘脑、尾状核、海马、壳核和伏隔核体积减少。运动外的临床表现主要为言语流畅性缺陷、语言障碍、淡漠和假性延髓情感。我们的临床和影像学评估证实了在基于人群的 PLS 患者队列中存在相当多的运动外变化。我们的数据表明,PLS 不应再被视为选择性影响锥体系统的神经退行性疾病。PLS 与广泛的运动外变化和表现有关,在这种发病率较低的情况下,应在多学科管理中仔细考虑这些变化和表现。