Motor Neuron dysfunction in frontotemporal dementia

被引:240
作者
Burrell, James R. [1 ,2 ]
Kiernan, Matthew C. [1 ,2 ]
Vucic, Steve [1 ,3 ]
Hodges, John R. [1 ]
机构
[1] Univ New S Wales, Neurosci Res Australia, Sydney, NSW 2031, Australia
[2] Univ New S Wales, Prince Wales Clin Sch, Sydney, NSW 2052, Australia
[3] Westmead Hosp, Sydney Med Sch, Wentworthville, NSW 2145, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
frontotemporal dementia; motor neuron disease; transcranial magnetic stimulation; biomarkers; AMYOTROPHIC-LATERAL-SCLEROSIS; TRANSCRANIAL MAGNETIC STIMULATION; PRIMARY-PROGRESSIVE-APHASIA; LOBAR DEGENERATION; CORTICAL HYPEREXCITABILITY; CORTICOBASAL DEGENERATION; THRESHOLD TRACKING; BRAIN ATROPHY; DISEASE; ALS;
D O I
10.1093/brain/awr195
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Frontotemporal dementia and motor neuron disease share clinical, genetic and pathological characteristics. Motor neuron disease develops in a proportion of patients with frontotemporal dementia, but the incidence, severity and functional significance of motor system dysfunction in patients with frontotemporal dementia has not been determined. Neurophysiological biomarkers have been developed to document motor system dysfunction including: short-interval intracortical inhibition, a marker of corticospinal motor neuron dysfunction and the neurophysiological index, a marker of lower motor neuron dysfunction. The present study performed detailed clinical and neurophysiological assessments on 108 participants including 40 consecutive patients with frontotemporal dementia, 42 age- and gender-matched patients with motor neuron disease and 26 control subjects. Of the 40 patients with frontotemporal dementia, 12.5% had concomitant motor neuron disease. A further 27.3% of the patients with frontotemporal dementia had clinical evidence of minor motor system dysfunction such as occasional fasciculations, mild wasting or weakness. Biomarkers of motor system function were abnormal in frontotemporal dementia. Average short-interval intracortical inhibition was reduced in frontotemporal dementia (4.3 +/- 1.7%) compared with controls (9.1 +/- 1.1%, P < 0.05). Short-interval intracortical inhibition was particularly reduced in the progressive non-fluent aphasia subgroup, but was normal in patients with behavioural variant frontotemporal dementia and semantic dementia. The neurophysiological index was reduced in frontotemporal dementia (1.1) compared with controls (1.9, P < 0.001), indicating a degree of lower motor neuron dysfunction, although remained relatively preserved when compared with motor neuron disease (0.7, P < 0.05). Motor system dysfunction in frontotemporal dementia may result from pathological involvement of the primary motor cortex, with secondary degeneration of lower motor neurons in the brainstem and anterior horn of the spinal cord.
引用
收藏
页码:2582 / 2594
页数:13
相关论文
共 70 条
[1]   The contribution of TMS to frontotemporal dementia variants [J].
Alberici, A. ;
Bonato, C. ;
Calabria, M. ;
Agosti, C. ;
Zanetti, O. ;
Miniussi, C. ;
Padovani, A. ;
Rossini, P. M. ;
Borroni, B. .
ACTA NEUROLOGICA SCANDINAVICA, 2008, 118 (04) :275-280
[2]   Selective impairment of verb processing associated with pathological changes in Brodmann areas 44 and 45 in the motor neurone disease-dementia-aphasia syndrome [J].
Bak, TH ;
O'Donovan, DG ;
Xuereb, JH ;
Boniface, S ;
Hodges, JR .
BRAIN, 2001, 124 :103-120
[3]   TARDBP Mutations in Motoneuron Disease with Frontotemporal Lobar Degeneration [J].
Benajiba, Lina ;
Le Ber, Isabelle ;
Camuzat, Agnes ;
Lacoste, Mathieu ;
Thomas-Anterion, Catherine ;
Couratier, Philippe ;
Legallic, Solenn ;
Salachas, Francois ;
Hannequin, Didier ;
Decousus, Marielle ;
Lacomblez, Lucette ;
Guedj, Eric ;
Golfier, Veronique ;
Camu, William ;
Dubois, Bruno ;
Campion, Dominique ;
Meininger, Vincent ;
Brice, Alexis .
ANNALS OF NEUROLOGY, 2009, 65 (04) :470-474
[4]   FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis [J].
Blair, Ian P. ;
Williams, Kelly L. ;
Warraich, Sadaf T. ;
Durnall, Jennifer C. ;
Thoeng, Annora D. ;
Manavis, Jim ;
Blumbergs, Peter C. ;
Vucic, Steve ;
Kiernan, Matthew C. ;
Nicholson, Garth A. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2010, 81 (06) :639-645
[5]   Mutation within TARDBP Leads to Frontotemporal Dementia without Motor Neuron Disease [J].
Borroni, B. ;
Bonvicini, C. ;
Alberici, A. ;
Buratti, E. ;
Agosti, C. ;
Archetti, S. ;
Papetti, A. ;
Stuani, C. ;
Di Luca, M. ;
Gennarelli, M. ;
Padovani, A. .
HUMAN MUTATION, 2009, 30 (11) :E974-E983
[6]   Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family [J].
Boxer, Adam L. ;
Mackenzie, Ian R. ;
Boeve, Bradley F. ;
Baker, Matthew ;
Seeley, William W. ;
Crook, Richard ;
Feldman, Howard ;
Hsiung, Ging-Yuek R. ;
Rutherford, Nicola ;
Laluz, Victor ;
Whitwell, Jennifer ;
Foti, Dean ;
McDade, Eric ;
Molano, Jennifer ;
Karydas, Anna ;
Wojtas, Aleksandra ;
Goldman, Jill ;
Mirsky, Jacob ;
Sengdy, Pheth ;
DeArmond, Stephen ;
Miller, Bruce L. ;
Rademakers, Rosa .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2011, 82 (02) :196-203
[7]   El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis [J].
Brooks, BR ;
Miller, RG ;
Swash, M ;
Munsat, TL .
AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS, 2000, 1 (05) :293-299
[8]   Isolated bulbar phenotype of amyotrophic lateral sclerosis [J].
Burrell, James R. ;
Vucic, Steve ;
Kiernan, Matthew C. .
AMYOTROPHIC LATERAL SCLEROSIS, 2011, 12 (04) :283-289
[9]   Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration [J].
Cairns, Nigel J. ;
Bigio, Eileen H. ;
Mackenzie, Ian R. A. ;
Neumann, Manuela ;
Lee, Virginia M. -Y. ;
Hatanpaa, Kimmo J. ;
White, Charles L., III ;
Schneider, Julie A. ;
Grinberg, Lea Tenenholz ;
Halliday, Glenda ;
Duyckaerts, Charles ;
Lowe, James S. ;
Holm, Ida E. ;
Tolnay, Markus ;
Okamoto, Koichi ;
Yokoo, Hideaki ;
Murayama, Shigeo ;
Woulfe, John ;
Munoz, David G. ;
Dickson, Dennis W. ;
Ince, Paul G. ;
Trojanowski, John Q. ;
Mann, David M. A. .
ACTA NEUROPATHOLOGICA, 2007, 114 (01) :5-22
[10]  
CANTELLO R, 1992, NEUROLOGY, V42, P1951