Brain surface contraction mapped in first-episode schizophrenia: a longitudinal magnetic resonance imaging study.
Brain surface contraction mapped in first-episode schizophrenia: a longitudinal magnetic resonance imaging study.
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脑表面收缩映射在第一期精神分裂症中:一项纵向磁共振成像研究。
DOI:
10.1038/mp.2008.34
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发表时间:
2009-10
影响因子:
11
通讯作者:
中科院分区:
文献类型:
--
作者:
Schizophrenia is associated with structural brain abnormalities, but the timing of onset and course of these changes remains unclear. Longitudinal magnetic resonance imaging (MRI) studies have demonstrated progressive brain volume decreases in patients around and after the onset of illness, although considerable discrepancies exist regarding which brain regions are affected. The anatomical pattern of these progressive changes in schizophrenia is largely unknown. In this study, MRI scans were acquired repeatedly from 16 schizophrenia patients approximately 2 years apart following their first episode of illness, and also from 14 age-matched healthy subjects. Cortical Pattern Matching, in combination with Structural Image Evaluation, using Normalisation, of Atrophy, was applied to compare the rates of cortical surface contraction between patients and controls. Surface contraction in the dorsal surfaces of the frontal lobe was significantly greater in patients with first-episode schizophrenia (FESZ) compared with healthy controls. Overall, brain surface contraction in patients and healthy controls showed similar anatomical patterns, with that of the former group exaggerated in magnitude across the entire brain surface. That the pattern of structural change in the early course of schizophrenia corresponds so closely to that associated with normal development is consistent with the hypothesis that a schizophrenia-related factor interacts with normal adolescent brain developmental processes in the pathophysiology of schizophrenia. The exaggerated progressive changes seen in patients with schizophrenia may reflect an increased rate of synaptic pruning, resulting in excessive loss of neuronal connectivity, as predicted by the late neurodevelopmental hypothesis of the illness.
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DOI:
10.1073/pnas.0402680101
发表时间:
2004-05-25
影响因子:
11.1
作者:
Gogtay, N;Giedd, JN;Thompson, PM
通讯作者:
Thompson, PM
DOI:
10.1073/pnas.111134598
发表时间:
2001-06-05
影响因子:
11.1
作者:
Egan, MF;Goldberg, TE;Weinberger, DR
通讯作者:
Weinberger, DR
影响因子:
14.5
作者:
Nakamura, Motoaki;Nestor, Paul G.;Shenton, Martha E.
通讯作者:
Shenton, Martha E.
影响因子:
--
作者:
Lieberman, JA;Tollefson, GD;Tohen, M
通讯作者:
Tohen, M
影响因子:
5.7
作者:
Genovese, CR;Lazar, NA;Nichols, T
通讯作者:
Nichols, T