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额颞叶变性中的锥体外系综合征。

Extrapyramidal syndromes in frontotemporal degeneration.

机构信息

Department of Neurology, University of Western Ontario, London, ON, Canada.

出版信息

J Mol Neurosci. 2011 Nov;45(3):336-42. doi: 10.1007/s12031-011-9616-1. Epub 2011 Sep 2.

DOI:10.1007/s12031-011-9616-1
PMID:21887521
Abstract

Descriptions of extrapyramidal (EP) involvement in Pick's disease (renamed recently as FTD) appeared 80 years ago. CBD pathology was confirmed as a common substrate for primary progressive aphasia (PPA). We suggested that CBD and PPA should be included with frontal lobe dementia as Pick complex. PSP was prototype for "subcortical dementia", and aphasia and apraxia, considered unusual for PSP, are now seen as a rule. The overlap of PSP and CBD is considerable. We recently reviewed our cohort with EPS in FTD and identified 22 patients with the movement disorder as a first syndrome and another larger group of 48 patients who developed EPS after an initial onset with a cognitive disorder: aphasic, behavioral or both. All cognitive onset CBD/PSP patients and all but two with motor onset developed aphasia during the course of their illness. General cognitive and behavioral measures are similar for each presentation, but language scores are worse in cognitive onset cases, reflecting the frequency of aphasic presentations. Anomic patients become non-fluent, logopenic, agrammatic and mute. Using the Frontal Behavioral Inventory (FBI), a questionnaire specifically designed for the spectrum of apathy and disinhibition displayed by patients with FTD, we have documented the behavior change in CBD/PSP with motor and cognitive onsets. The significant personality changes consisted of apathy, disinhibition, perseveration and inattention, some of the core symptoms of FTD. In 18 autopsied cases, 15 had tau pathology. The overlap of CBD/PSP with PPA and bvFTD suggests a spectrum of related entities and predicts tau-positive pathology. Cross-sectional studies without significant follow-up may not observe the subsequent development language or behavior deficit, or the evolution from PPA and/or FTD-bv to CBD/PSP.

摘要

描述锥体外系(EP)参与皮克病(最近更名为 FTD)的情况出现于 80 年前。CBD 病理学被证实为原发性进行性失语症(PPA)的常见基础。我们建议将 CBD 和 PPA 与额颞叶痴呆一起归入皮克综合征。PSP 是“皮质下痴呆”的原型,而之前认为在 PSP 中不常见的失语症和失用症,现在则被视为常见症状。PSP 和 CBD 有相当大的重叠。我们最近回顾了我们的 FTD 伴有 EPS 队列,并确定了 22 名以运动障碍为首发综合征的患者,以及另一组更大的 48 名患者,他们在以认知障碍(失语症、行为障碍或两者兼有)首发后出现了 EPS。所有认知障碍起病的 CBD/PSP 患者和除了两个运动障碍起病的患者外,在疾病过程中都出现了失语症。每种表现的总体认知和行为测量相似,但认知障碍起病的病例语言评分更差,反映了失语症表现的频率。命名性失语症患者会变得不流畅、失语法、语法错误和缄默。我们使用专门为 FTD 患者的淡漠和抑制障碍谱设计的问卷——额叶行为量表(FBI),记录了伴有运动和认知障碍起病的 CBD/PSP 的行为变化。显著的人格变化包括淡漠、抑制、固执和注意力不集中,这些都是 FTD 的核心症状。在 18 例尸检病例中,15 例存在 tau 病理学。CBD/PSP 与 PPA 和 bvFTD 的重叠表明存在一系列相关实体,并预测 tau 阳性病理学。没有显著随访的横断面研究可能无法观察到随后的语言或行为缺陷,或从 PPA 和/或 FTD-bv 向 CBD/PSP 的演变。

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Neuropathology of variants of progressive supranuclear palsy.进行性核上性麻痹的变异型神经病理学。
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2
Does corticobasal degeneration exist? A clinicopathological re-evaluation.皮质基底节变性是否存在?临床病理再评估。
Brain. 2010 Jul;133(Pt 7):2045-57. doi: 10.1093/brain/awq123.
3
Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsy.TDP-43 磷酸化病理与进行性核上性麻痹的海马硬化。
遗传性额颞叶痴呆的运动症状:为临床评定量表开发新模块。
J Neurol. 2023 Mar;270(3):1466-1477. doi: 10.1007/s00415-022-11442-y. Epub 2022 Nov 17.
4
Parkin beyond Parkinson's Disease-A Functional Meaning of Parkin Downregulation in TDP-43 Proteinopathies.帕金森病之外的 Parkin——Parkin 下调在 TDP-43 蛋白病中的功能意义。
Cells. 2021 Dec 1;10(12):3389. doi: 10.3390/cells10123389.
5
Pharmacotherapy for Neuropsychiatric Symptoms in Frontotemporal Dementia.额颞叶痴呆的神经精神症状的药物治疗。
CNS Drugs. 2021 Oct;35(10):1081-1096. doi: 10.1007/s40263-021-00854-5. Epub 2021 Aug 24.
6
Incidence of frontotemporal disorders in Olmsted County: A population-based study.奥姆斯特德县额颞叶疾病的发病率:一项基于人群的研究。
Alzheimers Dement. 2020 Mar;16(3):482-490. doi: 10.1016/j.jalz.2019.08.199. Epub 2020 Jan 4.
7
Lysosomal Dysfunction at the Centre of Parkinson's Disease and Frontotemporal Dementia/Amyotrophic Lateral Sclerosis.溶酶体功能障碍与帕金森病、额颞叶痴呆/肌萎缩性侧索硬化症的中心地位。
Trends Neurosci. 2019 Dec;42(12):899-912. doi: 10.1016/j.tins.2019.10.002. Epub 2019 Nov 5.
8
Prognostic importance of apathy in syndromes associated with frontotemporal lobar degeneration.淡漠在额颞叶变性相关综合征中的预后意义。
Neurology. 2019 Apr 2;92(14):e1547-e1557. doi: 10.1212/WNL.0000000000007249. Epub 2019 Mar 6.
9
Scales to Assess Clinical Features of Progressive Supranuclear Palsy: MDS Task Force Report.评估进行性核上性麻痹临床特征的量表:MDS特别工作组报告
Mov Disord Clin Pract. 2015 May 22;2(2):127-134. doi: 10.1002/mdc3.12130. eCollection 2015 Jun.
10
Neurotransmitter deficits from frontotemporal lobar degeneration.来自额颞叶变性的神经递质缺失。
Brain. 2018 May 1;141(5):1263-1285. doi: 10.1093/brain/awx327.
Acta Neuropathol. 2010 Jul;120(1):55-66. doi: 10.1007/s00401-010-0702-1. Epub 2010 May 30.
4
Leucine-rich repeat kinase 2 gene-associated disease: redefining genotype-phenotype correlation.富含亮氨酸重复激酶 2 基因相关疾病:重新定义基因型-表型相关性。
Neurodegener Dis. 2010;7(1-3):175-9. doi: 10.1159/000289232. Epub 2010 Mar 3.
5
The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration.原纤维蛋白中的突变谱:一项筛查545例神经退行性疾病的合作研究
Arch Neurol. 2010 Feb;67(2):161-70. doi: 10.1001/archneurol.2009.328.
6
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.与额颞叶痴呆、核上性凝视麻痹和舞蹈症相关的TARDBP变异
Mov Disord. 2009 Sep 15;24(12):1843-7. doi: 10.1002/mds.22697.
7
Progressive supranuclear palsy: a review of co-existing neurodegeneration.进行性核上性麻痹:并存神经退行性变的综述
Can J Neurol Sci. 2008 Nov;35(5):602-8. doi: 10.1017/s0317167100009392.
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J Neuropathol Exp Neurol. 2007 Oct;66(10):892-900. doi: 10.1097/nen.0b013e3181567873.
9
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Alzheimer Dis Assoc Disord. 2007 Apr-Jun;21(2):155-63. doi: 10.1097/WAD.0b013e31806547eb.
10
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Nat Clin Pract Neurol. 2006 Dec;2(12):658-65. doi: 10.1038/ncpneuro0357.