Frontotemporal white matter changes in amyotrophic lateral sclerosis.

作者: Sharon Abrahams , Laura H. Goldstein , John Suckling , Virginia Ng , Andy Simmons

DOI: 10.1007/S00415-005-0646-X

关键词:

摘要: Cognitive dysfunction can occur in some patients with amyotrophic lateral sclerosis (ALS) who are not suffering from dementia. The most striking and consistent cognitive deficit has been found using tests of verbal fluency. ALS fluency deficits have shown functional imaging abnormalities predominantly frontotemporal regions positron emission tomography (PET). This study used automated volumetric voxel-based analysis grey white matter densities structural magnetic resonance (MRI) scans to explore the underlying pattern cerebral change nondemented deficits. Two groups patients, defined by presence or absence impairment on basis Written Verbal Fluency Test (ALSi, cognitively impaired, n = 11; ALSu, unimpaired 12) were compared healthy age matched controls (n 12). A comparison ALSi group revealed significantly (p < 0.002) reduced volume extensive motor non–motor regions, including corresponding association fibres. These demonstrated a profile executive memory dysfunction. Less reductions ALSu control frontal White volumes also correlate performance tests. There no significant either patient controls. temporal here may underlie previously reported non–demented patients. results suggest that extra–motor be present evidence change. findings support hypothesis continuum this disorder.

参考文章(38)
Hiroshi Yamauchi, Hidenao Fukuyama, Yasuomi Ouchi, Yasuhiro Nagahama, Jun Kimura, Reinin Asato, Junji Konishi, Corpus callosum atrophy in amyotrophic lateral sclerosis Journal of the Neurological Sciences. ,vol. 134, pp. 189- 196 ,(1995) , 10.1016/0022-510X(95)00220-6
E. Andreadou, P. Sgouropoulos, P. Varelas, A. Gouliamos, C. Papageorgiou, Subcortical frontal lesions on MRI in patients with motor neurone disease Neuroradiology. ,vol. 40, pp. 298- 302 ,(1998) , 10.1007/S002340050588
C. R. Reynolds, J. Powel, Wechsler memory scale-revised Archives of Clinical Neuropsychology. ,vol. 3, pp. 397- 403 ,(1988) , 10.1093/ARCLIN/3.4.397
Koichi Okamoto, Shunsaku Hirai, Tsuneo Yamazaki, Xiaoyan Sun, Yoichi Nakazato, New ubiquitin-positive intraneuronal inclusions in the extra-motor cortices in patients with amyotrophic lateral sclerosis Neuroscience Letters. ,vol. 129, pp. 233- 236 ,(1991) , 10.1016/0304-3940(91)90469-A
A. C. Ludolph, K. J. Langen, M. Regard, H. Herzog, B. Kemper, T. Kuwert, I. G. Böttger, L. Feinendegen, Frontal lobe function in amyotrophic lateral sclerosis: a neuropsychologic and positron emission tomography study. Acta Neurologica Scandinavica. ,vol. 85, pp. 81- 89 ,(1992) , 10.1111/J.1600-0404.1992.TB04003.X
Douglas S. Goodin, Howard A. Rowley, Richard K. Olney, Magnetic resonance imaging in amyotrophic lateral sclerosis. Annals of Neurology. ,vol. 23, pp. 418- 420 ,(1988) , 10.1002/ANA.410230424
Arthur L. Benton, Visuospatial Judgment: A Clinical Test JAMA Neurology. ,vol. 35, pp. 364- 367 ,(1978) , 10.1001/ARCHNEUR.1978.00500300038006
J. Suckling, M.J. Brammer, A. Lingford-Hughes, E.T. Bullmore, Removal of extracerebral tissues in dual-echo magnetic resonance images via linear scale-space features Magnetic Resonance Imaging. ,vol. 17, pp. 247- 256 ,(1999) , 10.1016/S0730-725X(98)00099-X
P J Massman, J Sims, N Cooke, L J Haverkamp, V Appel, S H Appel, Prevalence and correlates of neuropsychological deficits in amyotrophic lateral sclerosis. Journal of Neurology, Neurosurgery, and Psychiatry. ,vol. 61, pp. 450- 455 ,(1996) , 10.1136/JNNP.61.5.450
J. A. Kiernan, J. Hudson, Frontal lobe atrophy in motor neuron diseases. Brain. ,vol. 117, pp. 747- 757 ,(1994) , 10.1093/BRAIN/117.4.747