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肌萎缩侧索硬化症及其他运动神经元疾病中的感觉功能障碍:临床相关性、组织病理学、神经生理学及神经影像学见解

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

作者信息

Kleinerova Jana, Chipika Rangariroyashe H, Tan Ee Ling, Yunusova Yana, Marchand-Pauvert Véronique, Kassubek Jan, Pradat Pierre-Francois, Bede Peter

机构信息

Computational Neuroimaging Group, School of Medicine, Trinity College Dublin, D02 PN40 Dublin, Ireland.

Department of Speech-Language Pathology, University of Toronto, Toronto, ON M5S 1A1, Canada.

出版信息

Biomedicines. 2025 Feb 22;13(3):559. doi: 10.3390/biomedicines13030559.

Abstract

: The clinical profiles of MNDs are dominated by inexorable motor decline, but subclinical proprioceptive, nociceptive and somatosensory deficits may also exacerbate mobility, dexterity, and bulbar function. While extra-motor pathology and frontotemporal involvement are widely recognised in motor neuron diseases (MNDs), reports of sensory involvement are conflicting. The potential contribution of sensory deficits to clinical disability is not firmly established and the spectrum of sensory manifestations is poorly characterised. : A systematic review was conducted to examine the clinical, neuroimaging, electrophysiology and neuropathology evidence for sensory dysfunction in MND phenotypes. : In ALS, paraesthesia, pain, proprioceptive deficits and taste alterations are sporadically reported and there is also compelling electrophysiological, histological and imaging evidence of sensory network alterations. Gait impairment, impaired dexterity, and poor balance in ALS are likely to be multifactorial, with extrapyramidal, cerebellar, proprioceptive and vestibular deficits at play. Human imaging studies and animal models also confirm dorsal column-medial lemniscus pathway involvement as part of the disease process. Sensory symptoms are relatively common in spinal and bulbar muscular atrophy (SBMA) and Hereditary Spastic Paraplegia (HSP), but are inconsistently reported in primary lateral sclerosis (PLS) and in post-poliomyelitis syndrome (PPS). : Establishing the prevalence and nature of sensory dysfunction across the spectrum of MNDs has a dual clinical and academic relevance. From a clinical perspective, subtle sensory deficits are likely to impact the disability profile and care needs of patients with MND. From an academic standpoint, sensory networks may be ideally suited to evaluate propagation patterns and the involvement of subcortical grey matter structures. Our review suggests that sensory dysfunction is an important albeit under-recognised facet of MND.

摘要

运动神经元病(MNDs)的临床特征主要表现为不可阻挡的运动功能衰退,但亚临床本体感觉、伤害性感觉和躯体感觉缺陷也可能会加重活动能力、灵活性及延髓功能。虽然运动神经元病(MNDs)中运动外病理改变和额颞叶受累已得到广泛认可,但关于感觉受累的报道却相互矛盾。感觉缺陷对临床残疾的潜在影响尚未得到确切证实,感觉表现的范围也缺乏明确的特征描述。

开展了一项系统综述,以研究MND表型中感觉功能障碍的临床、神经影像学、电生理学和神经病理学证据。

在肌萎缩侧索硬化症(ALS)中,偶有关于感觉异常、疼痛、本体感觉缺陷和味觉改变的报道,同时也有令人信服的电生理学、组织学和影像学证据表明存在感觉网络改变。ALS患者的步态障碍、灵活性受损和平衡能力差可能是多因素导致的,锥体外系、小脑、本体感觉和前庭功能缺陷都在其中起作用。人体影像学研究和动物模型也证实,背柱-内侧丘系通路受累是疾病过程的一部分。感觉症状在脊髓性和延髓性肌萎缩(SBMA)及遗传性痉挛性截瘫(HSP)中相对常见,但在原发性侧索硬化症(PLS)和小儿麻痹后遗症(PPS)中的报道并不一致。

确定MNDs全谱中感觉功能障碍的患病率和性质具有临床和学术双重意义。从临床角度来看,细微的感觉缺陷可能会影响MND患者的残疾状况和护理需求。从学术角度来看,感觉网络可能非常适合评估传播模式和皮质下灰质结构的受累情况。我们的综述表明,感觉功能障碍是MND一个重要但未得到充分认识的方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a1e/11940395/01f858fc3439/biomedicines-13-00559-g001.jpg

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