Behavioral and language variants of frontotemporal dementia: A review of key symptoms

被引:26
作者
Laforce, Robert, Jr. [1 ,2 ]
机构
[1] CHU Quebec, Clin Interdisciplinaire Memoire, Dept Neurol Sci, Quebec City, PQ, Canada
[2] Univ Laval, CHU Quebec, Fac Med, Quebec City, PQ G1J 1Z4, Canada
关键词
Frontotemporal dementia; Behavioral variant; Language variants; Symptoms; PRIMARY PROGRESSIVE APHASIA; LOBAR DEGENERATION; HEXANUCLEOTIDE REPEAT; ALZHEIMERS-DISEASE; SEMANTIC DEMENTIA; MUTATIONS; DIAGNOSIS; ABNORMALITIES; DYSFUNCTION; BIOMARKERS;
D O I
10.1016/j.clineuro.2013.09.031
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
While recent advances in the development of neuroimaging and molecular biomarkers for studying neurodegenerative conditions have revolutionized the field, dementia remains a clinical diagnosis. No component of the diagnostic process is more crucial than obtaining a good history. Getting to know the first manifestations of the disease, tracking their evolution and functional impact, combined with a targeted neurological examination, further guides differential diagnosis. This paper summarizes the key symptoms of the behavioral and language variants of frontotemporal dementia. The behavioral variant of frontotemporal dementia (bvFTD) is characterized by severe changes in behavior and personality such as disinhibition, apathy, loss of empathy, or stereotypic behavior, leading to a loss of social competence. Executive functions are impaired, while memory and visuospatial skills are relatively better preserved. By contrast, the language variants or primary progressive aphasias (PPAs) are marked by prominent language disturbances that can be subclassified into a non-fluent/agrammatic variant (naPPA), a semantic variant (svPPA), and a logopenic variant (IvPPA). Although combined characterization of clinical, imaging, biological and genetic biomarkers is essential to establish a detailed diagnosis of such heterogeneous conditions, the author emphasizes the importance of accurate recognition of key symptoms that can lead to better identification of underlying neuropathology and appropriate treatment approaches. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:2405 / 2410
页数:6
相关论文
共 64 条
  • [21] Semantic dementia: a unique clinicopathological syndrome
    Hodges, John R.
    Patterson, Karalyn
    [J]. LANCET NEUROLOGY, 2007, 6 (11) : 1004 - 1014
  • [22] Clinicopathological correlates in frontotemporal dementia
    Hodges, JR
    Davies, RR
    Xuereb, JH
    Casey, B
    Broe, M
    Bak, TH
    Kril, JJ
    Halliday, GM
    [J]. ANNALS OF NEUROLOGY, 2004, 56 (03) : 399 - 406
  • [23] Orbitofrontal Dysfunction Discriminates Behavioral Variant Frontotemporal Dementia from Alzheimer's Disease
    Hornberger, M.
    Savage, S.
    Hsieh, S.
    Mioshi, E.
    Piguet, O.
    Hodges, J. R.
    [J]. DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2010, 30 (06) : 547 - 552
  • [24] Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
    Hutton, M
    Lendon, CL
    Rizzu, P
    Baker, M
    Froelich, S
    Houlden, H
    Pickering-Brown, S
    Chakraverty, S
    Isaacs, A
    Grover, A
    Hackett, J
    Adamson, J
    Lincoln, S
    Dickson, D
    Davies, P
    Petersen, RC
    Stevens, M
    de Graaff, E
    Wauters, E
    van Baren, J
    Hillebrand, M
    Joosse, M
    Kwon, JM
    Nowotny, P
    Che, LK
    Norton, J
    Morris, JC
    Reed, LA
    Trojanowski, J
    Basun, H
    Lannfelt, L
    Neystat, M
    Fahn, S
    Dark, F
    Tannenberg, T
    Dodd, PR
    Hayward, N
    Kwok, JBJ
    Schofield, PR
    Andreadis, A
    Snowden, J
    Craufurd, D
    Neary, D
    Owen, F
    Oostra, BA
    Hardy, J
    Goate, A
    van Swieten, J
    Mann, D
    Lynch, T
    [J]. NATURE, 1998, 393 (6686) : 702 - 705
  • [25] Frontotemporal lobar degeneration - Demographic characteristics of 353 patients
    Johnson, JK
    Diehl, J
    Mendez, MF
    Neuhaus, J
    Shapira, JS
    Forman, M
    Chute, DJ
    Roberson, ED
    Pace-Savitsky, C
    Neumann, M
    Chow, TW
    Rosen, HJ
    Forstl, H
    Kurz, A
    Miller, BL
    [J]. ARCHIVES OF NEUROLOGY, 2005, 62 (06) : 925 - 930
  • [26] Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP
    Josephs, KA
    Petersen, RC
    Knopman, DS
    Boeve, BF
    Whitwell, JL
    Duffy, JR
    Parisi, JE
    Dickson, DW
    [J]. NEUROLOGY, 2006, 66 (01) : 41 - 48
  • [27] Characterizing a neurodegenerative syndrome: primary progressive apraxia of speech
    Josephs, Keith A.
    Duffy, Joseph R.
    Strand, Edythe A.
    Machulda, Mary M.
    Senjem, Matthew L.
    Master, Ankit V.
    Lowe, Val J.
    Jack, Clifford R., Jr.
    Whitwell, Jennifer L.
    [J]. BRAIN, 2012, 135 : 1522 - 1536
  • [28] The evolution and pathology of frontotemporal dementia
    Kertesz, A
    McMonagle, P
    Blair, M
    Davidson, W
    Munoz, DG
    [J]. BRAIN, 2005, 128 : 1996 - 2005
  • [29] Primary progressive aphasia and Pick complex
    Kertesz, A
    Munoz, DG
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 2003, 206 (01) : 97 - 107
  • [30] The incidence of frontotemporal lobar degeneration in Rochester, Minnesota, 1990 through 1994
    Knopman, DS
    Petersen, RC
    Edland, SD
    Cha, RH
    Rocca, WA
    [J]. NEUROLOGY, 2004, 62 (03) : 506 - 508