Tahedl Marlene, Kleinerova Jana, Doherty Mark A, Hengeveld Jennifer C, McLaughlin Russell L, Hardiman Orla, Tan Ee Ling, Bede Peter
Computational Neuroimaging Group (CNG), School of Medicine, Trinity College Dublin, Dublin, Ireland.
Complex Trait Genomics Laboratory, Smurfit Institute of Genetics, Trinity College Dublin, Dublin, Ireland.
Eur J Neurol. 2025 May;32(5):e70146. doi: 10.1111/ene.70146.
The thalamus is a key subcortical hub of numerous corticobasal and corticocortical circuits mediating a wealth of cognitive, behavioural, sensory and motor processes. While thalamic pathology is increasingly recognised in amyotrophic lateral sclerosis, its degeneration is often assessed in isolation instead of adopting a network-wise perspective and assessing the integrity of its rich cortical projections.
A prospective imaging study was conducted in a cohort of genetically stratified patients to assess the structural and functional integrity of thalamo-cortical circuits and volumetric alterations longitudinally.
The white matter integrity of thalamic projections to the anterior cingulate cortex, cerebellum, dorsolateral prefrontal cortex (DLPFC), Heschl's gyrus, medial frontal gyrus (MFG), orbitofrontal cortex, parietal cortex, postcentral gyrus and precentral gyrus (PreCG) is affected at baseline in ALS, which is more marked in C9orf72 hexanucleotide repeat carriers. Precentral gyrus and cerebellar grey matter volumes are also reduced, particularly in C9orf72. Longitudinal analyses capture progressive disconnection between the thalamus and frontal regions (DLPFC and MFG) in both C9orf72 positive and sporadic patients and progressive thalamo-PreCG disconnection in the sporadic C9orf72 negative cohort. Functional connectivity analyses revealed increasing thalamo-cerebellar connectivity in sporadic ALS and increasing thalamo-DLPFC connectivity in intermediate-length CAG repeat expansion carriers in ATXN2 over time.
Our data provide evidence of extensive thalamo-cortical connectivity alterations in ALS. Corticobasal circuits mediating extrapyramidal, somatosensory, cognitive and behavioural functions are increasingly affected as the disease progresses. The degeneration of thalamic projections support the conceptualisation of ALS as a 'network disease' and the notion of 'what wires together degenerates together'.
丘脑是众多皮质-基底节和皮质-皮质回路的关键皮质下枢纽,介导着丰富的认知、行为、感觉和运动过程。虽然在肌萎缩侧索硬化症中丘脑病变越来越受到认可,但其变性通常是孤立评估的,而不是从网络角度进行评估并评估其丰富的皮质投射的完整性。
对一组基因分层患者进行了一项前瞻性成像研究,以纵向评估丘脑-皮质回路的结构和功能完整性以及体积变化。
在肌萎缩侧索硬化症患者中,丘脑投射到前扣带回皮质、小脑、背外侧前额叶皮质(DLPFC)、颞横回、内侧前额叶皮质(MFG)、眶额皮质、顶叶皮质、中央后回和中央前回(PreCG)的白质完整性在基线时就受到影响,在C9orf72六核苷酸重复携带者中更为明显。中央前回和小脑灰质体积也减少,特别是在C9orf72基因携带者中。纵向分析发现,在C9orf72阳性和散发性患者中,丘脑与额叶区域(DLPFC和MFG)之间的连接逐渐断开,在散发性C9orf72阴性队列中,丘脑与中央前回之间的连接逐渐断开。功能连接分析显示,随着时间的推移,散发性肌萎缩侧索硬化症患者丘脑与小脑的连接增加,而在ATXN2基因中CAG重复序列中等长度扩展携带者中,丘脑与DLPFC的连接增加。
我们的数据提供了肌萎缩侧索硬化症中广泛的丘脑-皮质连接改变的证据。随着疾病进展,介导锥体外系、体感、认知和行为功能的皮质-基底节回路越来越受到影响。丘脑投射的变性支持了将肌萎缩侧索硬化症概念化为“网络疾病”以及“连接在一起的结构一起退化”的观点。