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本文引用的文献

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Cortico-Striatal-Thalamic Loop Circuits of the Salience Network: A Central Pathway in Psychiatric Disease and Treatment.突显网络的皮质-纹状体-丘脑环路:精神疾病与治疗的核心通路
Front Syst Neurosci. 2016 Dec 27;10:104. doi: 10.3389/fnsys.2016.00104. eCollection 2016.
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Grey and White Matter Clinico-Anatomical Correlates of Disinhibition in Neurodegenerative Disease.神经退行性疾病中去抑制的灰质和白质临床解剖学关联
PLoS One. 2016 Oct 10;11(10):e0164122. doi: 10.1371/journal.pone.0164122. eCollection 2016.
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Advances in neuroimaging in frontotemporal dementia.额颞叶痴呆的神经影像学进展
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Molecular neuropathology of frontotemporal dementia: insights into disease mechanisms from postmortem studies.额颞叶痴呆的分子神经病理学:来自尸检研究的疾病机制见解
J Neurochem. 2016 Aug;138 Suppl 1:54-70. doi: 10.1111/jnc.13588. Epub 2016 Jun 15.
5
Disease-specific patterns of cortical and subcortical degeneration in a longitudinal study of Alzheimer's disease and behavioural-variant frontotemporal dementia.阿尔茨海默病和行为变异型额颞叶痴呆纵向研究中皮质和皮质下变性的疾病特异性模式
Neuroimage. 2017 May 1;151:72-80. doi: 10.1016/j.neuroimage.2016.03.032. Epub 2016 Mar 21.
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Human Choice Strategy Varies with Anatomical Projections from Ventromedial Prefrontal Cortex to Medial Striatum.人类选择策略随腹内侧前额叶皮质到内侧纹状体的解剖投射而变化。
J Neurosci. 2016 Mar 9;36(10):2857-67. doi: 10.1523/JNEUROSCI.2033-15.2016.
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Cortical thickness changes in patients with Parkinson's disease and impulse control disorders.帕金森病伴冲动控制障碍患者的皮质厚度变化
Parkinsonism Relat Disord. 2016 Mar;24:119-25. doi: 10.1016/j.parkreldis.2015.10.013. Epub 2015 Oct 20.
8
Joint assessment of white matter integrity, cortical and subcortical atrophy to distinguish AD from behavioral variant FTD: A two-center study.联合评估白质完整性、皮质和皮质下萎缩以区分阿尔茨海默病与行为变异型额颞叶痴呆:一项双中心研究。
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An advanced white matter tract analysis in frontotemporal dementia and early-onset Alzheimer's disease.额颞叶痴呆和早发性阿尔茨海默病的高级白质束分析
Brain Imaging Behav. 2016 Dec;10(4):1038-1053. doi: 10.1007/s11682-015-9458-5.
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行为变异型额颞叶痴呆患者额纹状体和额丘脑通路上的区域性结构连接低下和连接过度。

Regional structural hypo- and hyperconnectivity of frontal-striatal and frontal-thalamic pathways in behavioral variant frontotemporal dementia.

机构信息

Graduate School of Medicine, University of Wollongong, Wollongong, Australia.

School of Medicine, The University of Notre Dame Australia, Fremantle, Australia; Clinical Research Centre, North Metropolitan Health Service - Mental Health, Perth, Australia.

出版信息

Hum Brain Mapp. 2018 Oct;39(10):4083-4093. doi: 10.1002/hbm.24233. Epub 2018 Jun 20.

DOI:10.1002/hbm.24233
PMID:29923666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6866429/
Abstract

Behavioral variant frontotemporal dementia (bvFTD) has been predominantly considered as a frontotemporal cortical disease, with limited direct investigation of frontal-subcortical connections. We aim to characterize the grey and white matter components of frontal-thalamic and frontal-striatal circuits in bvFTD. Twenty-four patients with bvFTD and 24 healthy controls underwent morphological and diffusion imaging. Subcortical structures were manually segmented according to published protocols. Probabilistic pathways were reconstructed separately from the dorsolateral, orbitofrontal and medial prefrontal cortex to the striatum and thalamus. Patients with bvFTD had smaller cortical and subcortical volumes, lower fractional anisotropy, and higher mean diffusivity metrics, which is consistent with disruptions in frontal-striatal-thalamic pathways. Unexpectedly, regional volumes of the striatum and thalamus connected to the medial prefrontal cortex were significantly larger in bvFTD (by 135% in the striatum, p = .032, and 217% in the thalamus, p = .004), despite smaller dorsolateral prefrontal cortex connected regional volumes (by 67% in the striatum, p = .002, and 65% in the thalamus, p = .020), and inconsistent changes in orbitofrontal cortex connected regions. These unanticipated findings may represent compensatory or maladaptive remodeling in bvFTD networks. Comparisons are made to other neuropsychiatric disorders suggesting a common mechanism of changes in frontal-subcortical networks; however, longitudinal studies are necessary to test this hypothesis.

摘要

行为变异型额颞叶痴呆(bvFTD)主要被认为是额颞皮质疾病,对额皮质下连接的直接研究有限。我们旨在描述 bvFTD 中额皮质-丘脑和额皮质-纹状体回路的灰质和白质成分。24 名 bvFTD 患者和 24 名健康对照者接受了形态学和弥散成像检查。根据已发表的方案手动分割皮质下结构。分别从前外侧、眶额和内侧前额皮质到纹状体和丘脑重建概率性通路。bvFTD 患者皮质和皮质下体积较小,各向异性分数较低,平均弥散度较高,这与额皮质-纹状体-丘脑通路中断一致。出乎意料的是,与内侧前额皮质相连的纹状体和丘脑的区域体积在 bvFTD 中明显更大(纹状体增加 135%,p=0.032,丘脑增加 217%,p=0.004),尽管与背外侧前额皮质相连的区域体积较小(纹状体减少 67%,p=0.002,丘脑减少 65%,p=0.020),且眶额皮质相连的区域变化不一致。这些意外的发现可能代表 bvFTD 网络中的代偿性或适应性重塑。与其他神经精神障碍进行了比较,表明额皮质下网络变化的共同机制;然而,需要进行纵向研究来检验这一假设。