Longitudinal cerebral diffusion changes reflect progressive decline of language and cognition

被引:5
|
作者
Frings, Lars [1 ,2 ,3 ]
Dressel, Katharina [4 ]
Abel, Stefanie [4 ,5 ]
Mader, Irina [6 ,7 ]
Glauche, Volkmar [7 ]
Weiller, Cornelius [7 ,8 ]
Huell, Michael [1 ,2 ]
机构
[1] Univ Freiburg, Univ Med Ctr, Ctr Geriatr & Gerontol Freiburg, Freiburg, Germany
[2] Univ Freiburg, Univ Med Ctr, Sect Geriatr Psychiat & Neuropsychol, Freiburg, Germany
[3] Univ Freiburg, Univ Med Ctr, Dept Radiat Oncol, Freiburg, Germany
[4] Univ Hosp RWTH Aachen, Clin & Cognit Neurosci CCN Sect, Aachen, Germany
[5] Univ Hosp RWTH Aachen, Neuropsychol Sect, Aachen, Germany
[6] Univ Freiburg, Univ Med Ctr, Sect Neuroradiol, Freiburg, Germany
[7] Univ Freiburg, Univ Med Ctr, Freiburg Brain Imaging, Freiburg, Germany
[8] Univ Freiburg, Univ Med Ctr, Dept Neurol, Freiburg, Germany
关键词
Diffusion tensor imaging; Voxel-based morphometry; Cognition; Language; Dementia; TEMPORAL-LOBE ATROPHY; SEMANTIC DEMENTIA; FRONTOTEMPORAL DEMENTIA; ALZHEIMERS-DISEASE; HUMAN BRAIN; APHASIA; COMPREHENSION; IMPAIRMENT; VARIANTS; REPRESENTATION;
D O I
10.1016/j.pscychresns.2013.08.003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Language deficits are regularly found in cortical neurodegenerative diseases. The progression of language deficits shows a considerable inter-individual variability even within one diagnostic group. We aimed at detecting patterns of altered diffusion as well as atrophy of cerebral gray and white matter which underlie ongoing language-related deterioration in patients with cortical neurodegenerative diseases. Diffusion tensor imaging and T1-weighted MRI data of 26 patients with clinically diagnosed neurodegenerative disorders were acquired at baseline and 14 months later in this prospective study. Language functions were assessed with a confrontation naming test and the Token Test. Diffusion and voxel-based morphometric measures were calculated and correlates of language performance were evaluated. Across all patients, the naming impairment was related to diffusion (false discovery rate-corrected P < 0.05 at baseline) and atrophy abnormalities (family-wise error (EWE)-corrected P < 0.05 at follow-up) primarily in the left temporal lobe. Deficits in the Token Test were correlated with predominantly left frontal MRI abnormalities (FWE-corrected P < 0.05). The Token Test performance decline over 14 months was accompanied by further increasing abnormalities in the frontal cortex, left caudate, parietal cortex (all FWE-corrected P < 0.05), and posterior callosal body (EWE-corrected P = 0.05 5). Both diffusion and structural MRI were apt to elucidate the underpinnings of inter-individual differences in language-related deficits and to detect longitudinal changes that accompanied ongoing cognition and language decline, with mean diffusivity appearing most sensitive. This might indicate the usefulness of diffusion measures as markers for successful intervention in therapy studies. (C) 2013 Elsevier Ireland Ltd. All rights reserved,
引用
收藏
页码:395 / 401
页数:7
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