Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions

被引:74
作者
Cairns, NJ [1 ]
Perry, RH
Jaros, E
Burn, D
McKeith, IG
Lowe, JS
Holton, J
Rossor, MN
Skullerud, K
Duyckaerts, C
Cruz-Sanchez, FF
Lantos, PL
机构
[1] Univ Penn, Sch Med, Ctr Neurodegenerat Dis Res, Philadelphia, PA 19104 USA
[2] Newcastle Gen Hosp, Dept Neuropathol, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
[3] Newcastle Gen Hosp, Inst Hlth Elderly, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
[4] Queens Med Ctr, Dept Pathol, Nottingham NG7 2UH, England
[5] UCL, Inst Neurol, Dept Neuropathol, London WC1N 3BG, England
[6] UCL, Inst Neurol, Dementia Res Grp, London WC1N 3BG, England
[7] Natl Hosp Norway, Dept Pathol, NO-0027 Oslo, Norway
[8] Hop La Pitie Salpetriere, Neuropathol Lab, F-75651 Paris 13, France
[9] Kings Coll London, Inst Psychiat, Dept Neuropathol, London SE5 8AF, England
关键词
neurodegeneration; neurofilament; neuronal cytoplasmic inclusion; dementia;
D O I
10.1016/S0304-3940(03)00100-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We report a new disease, dementia with neurofilament inclusions, characterized clinically by early-onset dementia with frontal lobe signs, focal atrophy of the frontal and temporal lobes, and microscopically by the presence in many brain regions of intraneuronal, cytoplasmic, neurofilament inclusions. The neuronal inclusions are immunoreactive to all three molecular weight neurofilament subunits: heavy (NF-H), light, and medium subunits, including the phosphorylated and non-phosphorylated forms of NF-H. Prion protein and beta-amyloid deposits were absent. The inclusions do not contain tau or alpha-synuclein protein aggregates known to characterize many neurodegenerative disorders. In addition to delineating a new disease entity, the identification of intraneuronal, cytoplasmic, neurofilament inclusions extends the molecular classification of neurodegenerative diseases and implicates new mechanisms of neurodegeneration in diseases affecting the human brain. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:177 / 180
页数:4
相关论文
共 27 条
  • [11] Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions
    Kertesz, A
    Kawarai, T
    Rogaeva, E
    St George-Hyslop, P
    Poorkaj, P
    Bird, TD
    Munoz, DG
    [J]. NEUROLOGY, 2000, 54 (04) : 818 - 827
  • [12] FAMILIAL DEMENTIA OF ADULT ONSET WITH PATHOLOGICAL FINDINGS OF A NONSPECIFIC NATURE
    KIM, RC
    COLLINS, GH
    PARISI, JE
    WRIGHT, AW
    CHU, YB
    [J]. BRAIN, 1981, 104 (MAR) : 61 - 78
  • [13] DEMENTIA LACKING DISTINCTIVE HISTOLOGIC FEATURES - A COMMON NON-ALZHEIMER DEGENERATIVE DEMENTIA
    KNOPMAN, DS
    MASTRI, AR
    FREY, WH
    SUNG, JH
    RUSTAN, T
    [J]. NEUROLOGY, 1990, 40 (02) : 251 - 256
  • [14] Neuropathologic variation in frontotemporal dementia due to the intronic tau 10+16 mutation
    Lantos, PL
    Cairns, NJ
    Khan, MN
    King, A
    Revesz, T
    Janssen, JC
    Morris, H
    Rossor, MN
    [J]. NEUROLOGY, 2002, 58 (08) : 1169 - 1175
  • [15] Neuronal intermediate filaments
    Lee, MK
    Cleveland, DW
    [J]. ANNUAL REVIEW OF NEUROSCIENCE, 1996, 19 : 187 - 217
  • [16] Neurodegenerative tauopathies
    Lee, VMY
    Goedert, M
    Trojanowski, JQ
    [J]. ANNUAL REVIEW OF NEUROSCIENCE, 2001, 24 : 1121 - 1159
  • [17] Molecular classification of the dementias
    Mann, DMA
    McDonagh, AM
    Snowden, J
    Neary, D
    Pickering-Brown, SM
    [J]. LANCET, 2000, 355 (9204) : 626 - 626
  • [18] Mann DMA, 1998, BRAIN PATHOL, V8, P325
  • [19] Polyglutamine pathogenesis
    Ross, CA
    Wood, JD
    Schilling, G
    Peters, MF
    Nucifora, FC
    Cooper, JK
    Sharp, AH
    Margolis, RL
    Borchelt, DR
    [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1999, 354 (1386) : 1005 - 1011
  • [20] Spillantini MG, 1998, BRAIN PATHOL, V8, P387