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肌萎缩侧索硬化症(ALS)中临床变量的灰质相关性:ALS 运动表型异质性和皮质局灶性的神经影像学研究。

Grey matter correlates of clinical variables in amyotrophic lateral sclerosis (ALS): a neuroimaging study of ALS motor phenotype heterogeneity and cortical focality.

机构信息

Trinity College Institute of Neuroscience (TCIN), Lloyd Building, Trinity College Dublin, Dublin, Ireland.

出版信息

J Neurol Neurosurg Psychiatry. 2013 Jul;84(7):766-73. doi: 10.1136/jnnp-2012-302674. Epub 2012 Oct 20.


DOI:10.1136/jnnp-2012-302674
PMID:23085933
Abstract

BACKGROUND: Body region of onset and functional disability are key components of disease heterogeneity in amyotrophic lateral sclerosis (ALS). OBJECTIVES: To evaluate patterns of grey matter pathology in the motor cortex and correlate focal structural changes with functional disability. METHODS: We conducted a single-centre neuroimaging study of a cohort of 33 cognitively normal patients with amyotrophic lateral sclerosis (ALS) and 44 healthy controls. A voxel-wise generalised linear model was used to investigate the distribution of disease burden within the motor cortex in relation to clinical disability. RESULTS: Patients with bulbar onset have bilateral focal atrophy in the bulbar segment of the motor homunculus compared with patients with limb onset who have focal cortical changes in the limb segment of their motor strip. Furthermore, the extent to which different body regions are affected in ALS corresponds to the extent of focal grey matter loss in the primary motor cortex. Cortical ALS pathology also extends beyond the motor cortex affecting frontal, occipital and temporal regions. CONCLUSIONS: Focal grey matter atrophy within the motor homunculus corresponds with functional disability in ALS. The findings support the existing concepts of cortical focality and motor phenotype heterogeneity in ALS.

摘要

背景:在肌萎缩侧索硬化症(ALS)中,发病部位和功能障碍是疾病异质性的关键组成部分。

目的:评估运动皮层灰质病理的模式,并将局灶性结构变化与功能障碍相关联。

方法:我们对 33 名认知正常的肌萎缩侧索硬化症(ALS)患者和 44 名健康对照者进行了单中心神经影像学研究。使用基于体素的广义线性模型来研究运动皮层内疾病负担的分布与临床残疾的关系。

结果:与上肢起病的患者相比,球部起病的患者在运动同形同构的球部节段存在双侧局灶性萎缩,而上肢起病的患者在运动带的上肢节段存在局灶性皮质改变。此外,ALS 不同身体部位受累的程度与初级运动皮层的局灶性灰质丧失程度相对应。皮层 ALS 病变还会扩展到运动皮层以外的额叶、枕叶和颞叶区域。

结论:运动同形同构内的局灶性灰质萎缩与 ALS 的功能障碍相对应。这些发现支持 ALS 中皮质局灶性和运动表型异质性的现有概念。

相似文献

[1]
Grey matter correlates of clinical variables in amyotrophic lateral sclerosis (ALS): a neuroimaging study of ALS motor phenotype heterogeneity and cortical focality.

J Neurol Neurosurg Psychiatry. 2012-10-20

[2]
Relationship between Clinical Parameters and Brain Structure in Sporadic Amyotrophic Lateral Sclerosis Patients According to Onset Type: A Voxel-Based Morphometric Study.

PLoS One. 2017-1-17

[3]
Cortical thinning and clinical heterogeneity in amyotrophic lateral sclerosis.

PLoS One. 2013-11-20

[4]
Focal thinning of the motor cortex mirrors clinical features of amyotrophic lateral sclerosis and their phenotypes: a neuroimaging study.

J Neurol. 2013-8-31

[5]
Structural explanation of poor prognosis of amyotrophic lateral sclerosis in the non-demented state.

Eur J Neurol. 2017-1

[6]
Structural and functional evaluation of cortical motor areas in Amyotrophic Lateral Sclerosis.

Exp Neurol. 2011-12-27

[7]
Brainstem pathology in amyotrophic lateral sclerosis and primary lateral sclerosis: A longitudinal neuroimaging study.

Neuroimage Clin. 2019-10-24

[8]
Exposing asymmetric gray matter vulnerability in amyotrophic lateral sclerosis.

Neuroimage Clin. 2015-3-14

[9]
Cortical Thinning Pattern of Bulbar- and Spinal-onset Amyotrophic Lateral Sclerosis: a Surface-based Morphometry Study.

Chin Med Sci J. 2018-6-30

[10]
Neuroimaging patterns along the ALS-FTD spectrum: a multiparametric imaging study.

Amyotroph Lateral Scler Frontotemporal Degener. 2017-11

引用本文的文献

[1]
Asymmetry in amyotrophic lateral sclerosis: Clinical, neuroimaging and histological observations.

Brain. 2025-8-1

[2]
Sensory Dysfunction in ALS and Other Motor Neuron Diseases: Clinical Relevance, Histopathology, Neurophysiology, and Insights from Neuroimaging.

Biomedicines. 2025-2-22

[3]
Neuroimaging correlates of domain-specific cognitive deficits in amyotrophic lateral sclerosis.

Neuroimage Clin. 2025

[4]
Neurofilament Light Chain Levels Interact with Neurodegenerative Patterns and Motor Neuron Dysfunction in Amyotrophic Lateral Sclerosis.

AJNR Am J Neuroradiol. 2024-4-8

[5]
Unraveling the Heterogeneity of ALS-A Call to Redefine Patient Stratification for Better Outcomes in Clinical Trials.

Cells. 2024-3-5

[6]
Premorbid brain structure influences risk of amyotrophic lateral sclerosis.

J Neurol Neurosurg Psychiatry. 2024-3-13

[7]
Brain imaging signatures in amyotrophic lateral sclerosis: Correlation with peripheral motor degeneration.

Ann Clin Transl Neurol. 2023-8

[8]
Aberrant Multimodal Connectivity Pattern Involved in Default Mode Network and Limbic Network in Amyotrophic Lateral Sclerosis.

Brain Sci. 2023-5-15

[9]
Brain metabolic signatures in patients with genetic and nongenetic amyotrophic lateral sclerosis.

CNS Neurosci Ther. 2023-9

[10]
Rate of speech decline in individuals with amyotrophic lateral sclerosis.

Sci Rep. 2022-9-20

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