Behavior and cognition in corticobasal degeneration and progressive supranuclear palsy

被引:77
作者
Kertesz, Andrew [1 ]
McMonagle, Paul [2 ]
机构
[1] Univ Western Ontario, St Josephs Hosp, Dept Cognit Neurol, London, ON N6A 4V2, Canada
[2] Royal Victoria Hosp, Dept Neurol, Belfast BT12 6BA, Antrim, North Ireland
关键词
Progressive supranuclear palsy; Corticobasal degeneration; Cognition; Behavior; Frontotemporal dementia; Aphasia; Apraxia; MULTIPLE SYSTEM ATROPHY; BRADYKINETIC-RIGID SYNDROMES; FRONTAL ASSESSMENT BATTERY; LIMB-KINETIC APRAXIA; GANGLIONIC DEGENERATION; SUBCORTICAL DEMENTIA; PARKINSONS-DISEASE; DIAGNOSTIC-CRITERIA; EXPLICIT MEMORY; BASAL GANGLIA;
D O I
10.1016/j.jns.2009.08.036
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD), previously described as Parkinsonian syndromes are also cognitive disorders, and biologically related to the frontotemporal dementia or Pick's disease PSP and CBD overlap clinically, pathologically and genetically, sharing tau haplotypes and mutations In our series of CBD/PSP patients with cognitive presentation (n = 36). primary progressive aphasia (PPA) was particularly common, but behavioral onset occurred also CBD or PSP as motor presentations developed significant language disorder in 17/19 The underlying pathology is predictably tau positive in these clinical combinations, regardless of the presentation Other cognitive features of CBDS include apraxia. alien hand and apathy, but often frontal lobe dementia with disinhibition develops also. CBDS also has visuospatial deficit. because of the parietal involvement. PSP was considered the prototype of subcortical dementia, with bradyphrenia, poor recall and executive deficit, but cortical features were recognized to be important also Language testing and a behavioral inventory should be part of neuropsychological tests to facilitate diagnosis and to quantify the deficit The clinical, genetic and pathological relationship is strong between CBD/PSP and the aphasic and behavioral components of the Pick complex. (C) 2009 Elsevier B.V All rights reserved
引用
收藏
页码:138 / 143
页数:6
相关论文
共 50 条
  • [41] Cerebral glucose metabolism in corticobasal degeneration: Comparison with progressive supranuclear palsy and normal controls
    Nagahama, Y
    Fukuyama, H
    Turjanski, N
    Kennedy, A
    Yamauchi, H
    Ouchi, Y
    Kimura, J
    Brooks, DJ
    Shibasaki, H
    MOVEMENT DISORDERS, 1997, 12 (05) : 691 - 696
  • [42] Proton magnetic resonance spectroscopic imaging in progressive supranuclear palsy, Parkinson's disease and corticobasal degeneration
    Tedeschi, G
    Litvan, I
    Bonavita, S
    Bertolino, A
    Lundbom, N
    Patronas, NJ
    Hallett, M
    BRAIN, 1997, 120 : 1541 - 1552
  • [43] Distal-proximal differences in limb apraxia in corticobasal degeneration but not progressive supranuclear palsy
    P. Soliveri
    S. Piacentini
    D. Paridi
    D. Testa
    F. Carella
    F. Girotti
    Neurological Sciences, 2003, 24 : 213 - 214
  • [44] Visual event-related potentials in progressive supranuclear palsy, corticobasal degeneration, striatonigral degeneration, and Parkinson's disease
    Lihong Wang
    Yoshiyuki Kuroiwa
    Toshiaki Kamitani
    Mei Li
    Tatsuya Takahashi
    Yume Suzuki
    Megumi Shimamura
    Osamu Hasegawa
    Journal of Neurology, 2000, 247 : 356 - 363
  • [45] Contribution of the astrocytic tau pathology to synapse loss in progressive supranuclear palsy and corticobasal degeneration
    Briel, Nils
    Pratsch, Katrin
    Roeber, Sigrun
    Arzberger, Thomas
    Herms, Jochen
    BRAIN PATHOLOGY, 2021, 31 (04)
  • [46] Motor neuron TDP-43 proteinopathy in progressive supranuclear palsy and corticobasal degeneration
    Riku, Yuichi
    Iwasaki, Yasushi
    Ishigaki, Shinsuke
    Akagi, Akio
    Hasegawa, Masato
    Nishioka, Kenya
    Li, Yuanzhe
    Riku, Miho
    Ikeuchi, Takeshi
    Fujioka, Yusuke
    Miyahara, Hiroaki
    Sone, Jun
    Hattori, Nobutaka
    Yoshida, Mari
    Katsuno, Masahisa
    Sobue, Gen
    BRAIN, 2022, 145 (08) : 2769 - 2784
  • [47] Clinical features differentiating patients with postmortem confirmed progressive supranuclear palsy and corticobasal degeneration
    I. Litvan
    D. A. Grimes
    A. E. Lang
    J. Jankovic
    A. McKee
    M. Verny
    K. Jellinger
    K. R. Chaudhuri
    R. K. B. Pearce
    Journal of Neurology, 1999, 246 (Suppl 2) : II1 - II5
  • [48] Clinical features differentiating patients with postmortem confirmed progressive supranuclear palsy and corticobasal degeneration
    Litvan, I
    Grimes, DA
    Lang, AE
    Jankovic, J
    McKee, A
    Verny, M
    Jellinger, K
    Chaudhuri, KR
    Pearce, RKB
    JOURNAL OF NEUROLOGY, 1999, 246 : 1 - 5
  • [49] Similarities and differences among progressive supranuclear palsy, corticobasal degeneration and Pick's disease
    Wakabayashi, K
    Takahashi, H
    NEUROPATHOLOGY, 1996, 16 (04) : 262 - 268
  • [50] A comparison of tau protein in cerebrospinal fluid between corticobasal degeneration and progressive supranuclear palsy
    Urakami, K
    Mori, M
    Wada, K
    Kowa, H
    Takeshima, T
    Arai, H
    Sasaki, H
    Kanai, M
    Shoji, M
    Ikemoto, K
    Morimatsu, M
    Hikasa, C
    Nakashima, K
    NEUROSCIENCE LETTERS, 1999, 259 (02) : 127 - 129