Progressive non-fluent aphasia is associated with hypometabolism centred on the left anterior insula

被引:254
作者
Nestor, PJ
Graham, NL
Fryer, TD
Williams, GB
Patterson, K
Hodges, JR
机构
[1] MRC, Cognit & Brain Sci Unit, Cambridge CB2 2EF, England
[2] Univ Cambridge, Neurol Unit, Cambridge, England
[3] Addenbrookes Hosp, Wolfson Brain Imaging Ctr, Cambridge, England
基金
英国医学研究理事会;
关键词
progressive non-fluent aphasia; PET; insula; voxel-based morphometry;
D O I
10.1093/brain/awg240
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Progressive non-fluent aphasia (PNFA) is a syndrome in which patients lose the ability to communicate fluently in the context of relative preservation of single word comprehension and non-linguistic cognitive abilities. Neuroimaging in case studies with PNFA has failed to identify a consistent neural substrate for the language disorder. In this study of a group of patients (n = 10) whose presenting complaint was progressive dysfluency, resting cerebral metabolism was measured using [(18)F]fluorodeoxyglucose-PET and analysed with the technique of statistical parametric mapping (SPM). Regional atrophy was assessed with voxel-based morphometry (VBM). Seven patients had a 'pure' PNFA syndrome, while the remaining three had additional features of a more pervasive dementia. Compared with controls, the patients showed hypometabolism in several regions that, most notably, included the left anterior insula/frontal opercular region. The VBM analysis revealed only one small area of atrophy in the left peri-Sylvian region. Analysis of the pure PNFA cases (n = 7) relative to controls yielded qualitatively similar results to those of the whole group, suggesting that these cases were also at risk of a more generalized dementia, a finding borne out in subsequent follow-up of two cases to date. The PNFA group was then compared with a group with Alzheimer's disease (n = 10) whose clinical profile did not include non-fluent aphasic features. In this analysis, the only persisting hypometabolic region was that centred over the left anterior insula. VBM did not identify any regional differences in atrophy between PNFA and Alzheimer's disease. In the light of current theories of fluent language production, the findings offer anatomical evidence that the breakdown in fluency is due to a motor articulatory planning deficit (speech apraxia) combined with a variable degree of agrammatism.
引用
收藏
页码:2406 / 2418
页数:13
相关论文
共 72 条
[1]   Imaging in primary progressive aphasia [J].
Abe, K ;
Ukita, H ;
Yanagihara, T .
NEURORADIOLOGY, 1997, 39 (08) :556-559
[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]   In vivo mapping of gray matter loss with voxel-based morphometry in mild Alzheimer's disease [J].
Baron, JC ;
Chételat, G ;
Desgranges, B ;
Perchey, G ;
Landeau, B ;
de la Sayette, V ;
Eustache, F .
NEUROIMAGE, 2001, 14 (02) :298-309
[4]   Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementia [J].
Basun, H ;
Almkvist, O ;
Axelman, K ;
Brun, A ;
Campbell, TA ;
Collinge, J ;
Forsell, C ;
Froelich, S ;
Wahlund, LO ;
Wetterberg, L ;
Lannfelt, L .
ARCHIVES OF NEUROLOGY, 1997, 54 (05) :539-544
[5]  
Bishop D., 1989, TEST RECEPTION GRAMM
[6]   Speech production: Wernicke, Broca and beyond [J].
Blank, S. Catrin ;
Scott, Sophie K. ;
Murphy, Kevin ;
Warburton, Elizabeth ;
Wise, Richard J. S. .
BRAIN, 2002, 125 :1829-1838
[7]   Non-verbal semantic impairment in semantic dementia [J].
Bozeat, S ;
Ralph, MAL ;
Patterson, K ;
Garrard, P ;
Hodges, JR .
NEUROPSYCHOLOGIA, 2000, 38 (09) :1207-1215
[8]  
Caplan D, 2000, HUM BRAIN MAPP, V9, P65
[9]  
CAPLAN LR, 1986, NEW ENGL J MED, V314, P1101
[10]   Varieties of progressive non-fluent aphasia [J].
Cappa, SF ;
Perani, D ;
Messa, C ;
Miozzo, A ;
Fazio, F .
NEUROBIOLOGY OF ALZHEIMER'S DISEASE, 1996, 777 :243-248