Semantic dementia: demography, familial factors and survival in a consecutive series of 100 cases

被引:196
作者
Hodges, John R. [1 ,2 ]
Mitchell, Jo [2 ]
Dawson, Kate [2 ]
Spillantini, Maria Grazia [2 ]
Xuereb, John H. [3 ]
McMonagle, Paul [3 ]
Nestor, Peter J. [2 ]
Patterson, Karalyn [4 ]
机构
[1] Univ New S Wales, POWMRI, Sydney, NSW 2031, Australia
[2] Addenbrookes Hosp, Univ Dept Clin Neurosci, Cambridge, England
[3] Univ Cambridge, Dept Pathol, Cambridge CB2 1TN, England
[4] MRC Cognit & Brain Sci Unit, Cambridge, England
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
frontotemporal dementia; semantic dementia; ubiquitin pathology; TDP43; FRONTOTEMPORAL LOBAR DEGENERATION; PRIMARY PROGRESSIVE APHASIA; COGNITIVE TEST BATTERY; ALZHEIMERS-DISEASE; TEMPORAL-LOBE; PREVALENCE; ATROPHY; IMPAIRMENT; MUTATIONS; PATTERNS;
D O I
10.1093/brain/awp248
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A great deal has been written about cognitive aspects of semantic dementia but little is known about the demography or prognosis. We describe these features in a consecutive series of 100 patients seen over a 17-year period; all cases were assessed and followed up in a specialist clinic. The mean age at diagnosis was 64.2 (+/- 7.1) range 40-79 years, but 46 presented after age 65 and 7 after 75; a higher proportion than the existing literature might predict. Fifteen had a first-degree relative with dementia, but in seven this was almost certainly unrelated. Only two had relatives with young-onset dementia. There were no families with more than two affected members. The familial rate was estimated at between 2% and 7% (95% confidence interval 0-12%). Kaplan-Meier analyses indicated a 50% survival of 12.8 years (95% confidence interval 11.9-13.7); a more benign course than suggested by neuropathologically based studies. We were unable to identify any factors influencing survival. Of the 100, 34 have died, with pathological confirmation in 24; 18 had frontotemporal lobar degeneration with ubiquitin-positive inclusions (13 of 13 confirmed TAR DNA binding protein-43 positive), and 3 had classic tau-positive Pick bodies and 3 had Alzheimer's pathology. The age at diagnosis or death across the pathological subgroups was equivalent. Although semantic dementia has a strong statistical association with ubiquitin-positive pathology, it does not have the signature of familial frontotemporal lobar degeneration with ubiquitin-positive inclusions, notably the presence of intranuclear lentiform TAR DNA binding protein-43 inclusions. The age of onset is older than predicted and the course more slowly progressive than suggested by earlier studies of small groups of subjects.
引用
收藏
页码:300 / 306
页数:7
相关论文
共 45 条
  • [1] Semantic dementia and fluent primary progressive aphasia: two sides of the same coin?
    Adlam, A.-L. R.
    Patterson, K.
    Rogers, T. T.
    Nestor, P. J.
    Salmond, C. H.
    Acosta-Cabronero, J.
    Hodges, J. R.
    [J]. BRAIN, 2006, 129 : 3066 - 3080
  • [2] Semantic knowledge in mild cognitive impairment and mild Alzheimer's disease
    Adlam, Anna-Lynne R.
    Bozeat, Sasha
    Arnold, Robert
    Watson, Peter
    Hodges, John R.
    [J]. CORTEX, 2006, 42 (05) : 675 - 684
  • [3] Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
    Baker, Matt
    Mackenzie, Ian R.
    Pickering-Brown, Stuart M.
    Gass, Jennifer
    Rademakers, Rosa
    Lindholm, Caroline
    Snowden, Julie
    Adamson, Jennifer
    Sadovnick, A. Dessa
    Rollinson, Sara
    Cannon, Ashley
    Dwosh, Emily
    Neary, David
    Melquist, Stacey
    Richardson, Anna
    Dickson, Dennis
    Berger, Zdenek
    Eriksen, Jason
    Robinson, Todd
    Zehr, Cynthia
    Dickey, Chad A.
    Crook, Richard
    McGowan, Eileen
    Mann, David
    Boeve, Bradley
    Feldman, Howard
    Hutton, Mike
    [J]. NATURE, 2006, 442 (7105) : 916 - 919
  • [4] Non-verbal semantic impairment in semantic dementia
    Bozeat, S
    Ralph, MAL
    Patterson, K
    Garrard, P
    Hodges, JR
    [J]. NEUROPSYCHOLOGIA, 2000, 38 (09) : 1207 - 1215
  • [5] Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
    Cruts, Marc
    Gijselinck, Ilse
    van der Zee, Julie
    Engelborghs, Sebastiaan
    Wils, Hans
    Pirici, Daniel
    Rademakers, Rosa
    Vandenberghe, Rik
    Dermaut, Bart
    Martin, Jean-Jacques
    van Duijn, Cornelia
    Peeters, Karin
    Sciot, Raf
    Santens, Patrick
    De Pooter, Tim
    Mattheijssens, Maria
    Van den Broeck, Marleen
    Cuijt, Ivy
    Vennekens, Krist'l
    De Deyn, Peter P.
    Kumar-Singh, Samir
    Van Broeckhoven, Christine
    [J]. NATURE, 2006, 442 (7105) : 920 - 924
  • [6] The neuropsychiatric inventory: Assessing psychopathology in dementia patients
    Cummings, JL
    [J]. NEUROLOGY, 1997, 48 (05) : S10 - S16
  • [7] The pathological basis of semantic dementia
    Davies, RR
    Hodges, JR
    Kril, JJ
    Patterson, K
    Halliday, GM
    Xuereb, JH
    [J]. BRAIN, 2005, 128 : 1984 - 1995
  • [8] The human perirhinal cortex and semantic memory
    Davies, RR
    Graham, KS
    Xuereb, JH
    Williams, GB
    Hodges, JR
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 2004, 20 (09) : 2441 - 2446
  • [9] Differing patterns of temporal atrophy in Alzheimer's disease and semantic dementia
    Galton, CJ
    Patterson, K
    Graham, K
    Lambon-Ralph, MA
    Williams, G
    Antoun, N
    Sahakian, BJ
    Hodges, JR
    [J]. NEUROLOGY, 2001, 57 (02) : 216 - 225
  • [10] Frontotemporal dementia with tau pathology
    Gasparini, Laura
    Terni, Beatrice
    Spillantini, Maria Grazia
    [J]. NEURODEGENERATIVE DISEASES, 2007, 4 (2-3) : 236 - 253