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行为变异型额颞叶痴呆中认知计时机制的退化

Degradation of cognitive timing mechanisms in behavioural variant frontotemporal dementia.

作者信息

Henley Susie M D, Downey Laura E, Nicholas Jennifer M, Kinnunen Kirsi M, Golden Hannah L, Buckley Aisling, Mahoney Colin J, Crutch Sebastian J

机构信息

Dementia Research Centre, Department of Neurodegenerative Disease, UCL Institute of Neurology, University College London, London WC1N 3BG, United Kingdom; National Hospital for Neurology and Neurosurgery, UCLH NHS Foundation Trust, Queens Square, London WC1N 3BG, United Kingdom.

Dementia Research Centre, Department of Neurodegenerative Disease, UCL Institute of Neurology, University College London, London WC1N 3BG, United Kingdom.

出版信息

Neuropsychologia. 2014 Dec;65:88-101. doi: 10.1016/j.neuropsychologia.2014.10.009. Epub 2014 Oct 19.

DOI:10.1016/j.neuropsychologia.2014.10.009
PMID:25447066
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4410788/
Abstract

The current study examined motor timing in frontotemporal dementia (FTD), which manifests as progressive deterioration in social, behavioural and cognitive functions. Twenty-patients fulfilling consensus clinical criteria for behavioural variant FTD (bvFTD), 11 patients fulfilling consensus clinical criteria for semantic-variant primary progressive aphasia (svPPA), four patients fulfilling criteria for nonfluent/agrammatic primary progressive aphasia (naPPA), eight patients fulfilling criteria for Alzheimer׳s disease (AD), and 31 controls were assessed on both an externally- and self-paced finger-tapping task requiring maintenance of a regular, 1500 ms beat over 50 taps. Grey and white matter correlates of deficits in motor timing were examined using voxel-based morphometry (VBM) and diffusion tensor imaging (DTI). bvFTD patients exhibited significant deficits in aspects of both externally- and self-paced tapping. Increased mean inter-response interval (faster than target tap time) in the self-paced task was associated with reduced grey matter volume in the cerebellum bilaterally, right middle temporal gyrus, and with increased axial diffusivity in the right superior longitudinal fasciculus, regions and tracts which have been suggested to be involved in a subcortical-cortical network of structures underlying timing abilities. This suggests that such structures can be affected in bvFTD, and that impaired motor timing may underlie some characteristics of the bvFTD phenotype.

摘要

当前研究考察了额颞叶痴呆(FTD)患者的运动定时,该病表现为社交、行为和认知功能的进行性衰退。对20例符合行为变异型FTD(bvFTD)共识临床标准的患者、11例符合语义变异型原发性进行性失语(svPPA)共识临床标准的患者、4例符合非流利/语法缺失型原发性进行性失语(naPPA)标准的患者、8例符合阿尔茨海默病(AD)标准的患者以及31名对照者进行了评估,评估内容为一项外部节奏和自我节奏的手指敲击任务,要求在50次敲击过程中保持1500毫秒的规律节拍。使用基于体素的形态测量法(VBM)和扩散张量成像(DTI)研究了运动定时缺陷的灰质和白质相关性。bvFTD患者在外部节奏和自我节奏敲击方面均表现出显著缺陷。自我节奏任务中平均反应间隔增加(快于目标敲击时间)与双侧小脑、右侧颞中回灰质体积减少以及右侧上纵束轴向扩散率增加有关,这些区域和神经束被认为参与了计时能力背后的皮质下-皮质结构网络。这表明这些结构在bvFTD中可能会受到影响,并且运动定时受损可能是bvFTD表型某些特征的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/4410788/b8b59949fce1/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/4410788/11e4e3bbc631/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/4410788/6444215d3bd7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/4410788/b8b59949fce1/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/4410788/11e4e3bbc631/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/4410788/6444215d3bd7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcd7/4410788/b8b59949fce1/gr3.jpg

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本文引用的文献

1
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Lancet Neurol. 2014 Jun;13(6):614-29. doi: 10.1016/S1474-4422(14)70090-0.
2
Permutation inference for the general linear model.一般线性模型的排列推断
Neuroimage. 2014 May 15;92(100):381-97. doi: 10.1016/j.neuroimage.2014.01.060. Epub 2014 Feb 11.
3
Dissociable neuroanatomical correlates of subsecond and suprasecond time perception.亚秒级和超秒级时间感知的可分离神经解剖学关联
手部动作的简短网络摄像头测试可预测认知无症状老年人社区样本中的情景记忆、执行功能和工作记忆。
Alzheimers Dement (Amst). 2024 Jan 25;16(1):e12520. doi: 10.1002/dad2.12520. eCollection 2024 Jan-Mar.
4
Investigating the associations between upper limb motor function and cognitive impairment: a scoping review.探讨上肢运动功能与认知障碍之间的关联:范围综述。
Geroscience. 2023 Dec;45(6):3449-3473. doi: 10.1007/s11357-023-00844-z. Epub 2023 Jun 20.
5
Sensorimotor Synchronization in Healthy Aging and Neurocognitive Disorders.健康衰老与神经认知障碍中的感觉运动同步
Front Psychol. 2022 Mar 17;13:838511. doi: 10.3389/fpsyg.2022.838511. eCollection 2022.
6
Subjective Time in Dementia: A Critical Review.痴呆症中的主观时间:一项批判性综述。
Brain Sci. 2021 Nov 12;11(11):1502. doi: 10.3390/brainsci11111502.
7
Speech and language impairments in behavioral variant frontotemporal dementia: A systematic review.行为变异型额颞叶痴呆的言语和语言障碍:系统评价。
Neurosci Biobehav Rev. 2021 Dec;131:1076-1095. doi: 10.1016/j.neubiorev.2021.10.015. Epub 2021 Oct 19.
8
Fractional Anisotropy in Selected, Motor-Related White Matter Tracts and Its Cross-Sectional and Longitudinal Associations With Motor Function in Healthy Older Adults.健康老年人中选定的与运动相关的白质纤维束的各向异性分数及其与运动功能的横断面和纵向关联
Front Hum Neurosci. 2021 Jun 22;15:621263. doi: 10.3389/fnhum.2021.621263. eCollection 2021.
9
Frontotemporal dementia patients exhibit deficits in predictive saccades.额颞叶痴呆患者在预测性扫视方面存在缺陷。
J Comput Neurosci. 2021 Aug;49(3):357-369. doi: 10.1007/s10827-020-00765-2. Epub 2020 Sep 18.
10
Behavioral rhythm and EEG rhythm to determine timing deficits in attention deficit hyperactivity disorder symptoms.行为节律和脑电图节律以确定注意力缺陷多动障碍症状中的时间缺陷。
Heliyon. 2020 Jul 29;6(7):e04546. doi: 10.1016/j.heliyon.2020.e04546. eCollection 2020 Jul.
J Cogn Neurosci. 2014 Aug;26(8):1685-93. doi: 10.1162/jocn_a_00580. Epub 2014 Jan 23.
4
White Matter Integrity of Specific Dentato-Thalamo-Cortical Pathways is Associated with Learning Gains in Precise Movement Timing.特定齿状核-丘脑-皮质通路的白质完整性与精确运动计时的学习增益相关。
Cereb Cortex. 2015 Jul;25(7):1707-14. doi: 10.1093/cercor/bht356. Epub 2014 Jan 16.
5
Timing functions of the cerebellum.小脑的时间功能。
J Cogn Neurosci. 1989 Spring;1(2):136-52. doi: 10.1162/jocn.1989.1.2.136.
6
In vivo and post-mortem memory circuit integrity in frontotemporal dementia and Alzheimer's disease.额颞叶痴呆和阿尔茨海默病患者体内和死后记忆回路完整性。
Brain. 2012 Oct;135(Pt 10):3015-25. doi: 10.1093/brain/aws239. Epub 2012 Sep 25.
7
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Alzheimers Res Ther. 2012 Sep 24;4(5):41. doi: 10.1186/alzrt144. eCollection 2012.
8
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J Alzheimers Dis. 2013;33(2):431-44. doi: 10.3233/JAD-2012-121156.
9
Functional anatomy of timing differs for production versus prediction of time intervals.时间的功能解剖在时间间隔的产生与预测方面存在差异。
Neuropsychologia. 2013 Jan;51(2):309-19. doi: 10.1016/j.neuropsychologia.2012.08.017. Epub 2012 Aug 30.
10
Learning about time: plastic changes and interindividual brain differences.学习时间:可塑性变化和个体间大脑差异。
Neuron. 2012 Aug 23;75(4):725-37. doi: 10.1016/j.neuron.2012.07.019.