Neuropathological abnormalities in schizophrenia: evidence from magnetization transfer imaging

被引:140
作者
Foong, J
Symms, MR
Barker, GJ
Maier, M
Woermann, FG
Miller, DH
Ron, MA
机构
[1] Inst Neurol, NMR Res Unit, London WC1N 3BG, England
[2] Univ London Imperial Coll Sci Technol & Med, Sch Med, London, England
[3] Gilead Hosp, Dept Psychiat, Bielefeld, Germany
[4] Mara Hosp, MRI Unit, Bielefeld, Germany
关键词
magnetization transfer imaging; magnetization transfer ratio; schizophrenia; neuropathological abnormalities;
D O I
10.1093/brain/124.5.882
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Post-mortem and structural brain imaging studies in schizophrenia have reported macroscopic changes such as global and regional cortical volume reductions, but it has been more difficult to characterize the histopathological changes that underlie these abnormalities. Magnetization transfer imaging (MTI), a novel MRI technique, more sensitive to subtle or early neuropathological changes than conventional MRI, provides a quantitative measure of macromolecular structural integrity represented by the magnetization transfer ratio (MTR), In this study, we used MTI to examine 25 patients with schizophrenia compared with 30 age-matched controls. A voxel-based analysis of the MTR maps revealed widespread MTR reductions in the cortex unrelated to volume reduction, predominantly in the frontal and temporal regions, in the schizophrenic patients when compared with controls. MTR reductions in bilateral parieto-occipital cortex and the genu of the corpus callosum were associated with the severity of negative symptoms in the schizophrenic patients, However, MTR changes were not related to other clinical variables of age, duration of illness and current dose of antipsychotic medication. This study demonstrates that MTR abnormalities in the cortex can be detected in chronic schizophrenia that may reflect subtle neuropathological changes involving neurones or neuronal processes, Longitudinal studies are needed to determine whether these abnormalities are related to disease progression or other disease manifestations such as cognitive changes.
引用
收藏
页码:882 / 892
页数:11
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