Frontal lobe N-acetylaspartate correlates with psychopathology in schizophrenia:: a proton magnetic resonance spectroscopy study

被引:56
作者
Sigmundsson, T
Maier, M
Toone, BK
Williams, SCR
Simmons, A
Greenwood, K
Ron, MA
机构
[1] UCL Hosp, Inst Neurol, Dept Neuropsychiat, London WC1N 3BG, England
[2] Kings Coll London, Inst Psychiat, Dept Psychol Med, London SE5 8AF, England
[3] Univ Hosp, Dept Psychiat, IS-101 Reykjavik, Iceland
[4] Univ London Imperial Coll Sci Technol & Med, Fac Med, Dept Psychol Med, London W6 8RP, England
[5] Kings Coll London, Inst Psychiat, Dept Clin Neurosci, London SE5 8AF, England
[6] Kings Coll London, Inst Psychiat, Dept Psychol, London SE5 8AF, England
关键词
frontal lobe; proton magnetic resonance spectroscopy ((1)H-MRS); schizophrenia; N-acetylaspartate (NAA); psychopathology;
D O I
10.1016/S0920-9964(02)00533-9
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Introduction: Clinical, neuropsychological and functional neuroimaging studies in schizophrenia suggest impaired frontal lobe function, especially of the dorsolateral prefrontal region (DLPFR). This dysfunction has in particular been associated with negative or "deficit" symptoms. Despite these findings, morphological studies have failed to show consistent structural abnormalities in the frontal lobe. This may be because existing techniques are not sensitive enough to detect structural abnormalities or that dysfunction in the frontal lobe is caused by lesions elsewhere. We used volume-localised proton magnetic resonance spectroscopy ((1)H-MRS) to measure N-acetylaspartate (NAA), a neuronal marker, to evaluate the neuronal integrity of the dorsolateral prefrontal region in schizophrenic patients with persistent negative symptoms and in healthy comparison subjects. Method: Twenty-five patients who fulfilled DSM-IV criteria for schizophrenia and met the criteria for the Deficit syndrome were compared to 26 healthy controls matched for age and gender. Bilateral proton MR spectra were collected from a 2-cm(3) volume in the dorsolateral prefrontal region and the absolute concentrations of N-acetylaspartate, choline (Cho) and creatine + phosphocreatine (Cr + PCr) were measured. Results: There was a significant negative correlation between severity of symptoms and NAA concentration in the schizophrenic patients. This was more marked for positive symptoms and for general psychopathology than for negative symptoms. There was also a significant correlation between NAA concentration and social functioning within the schizophrenic group. There were no significant differences between the two groups for the three metabolites. Conclusions: The negative association between severity of symptoms and NAA in schizophrenic patients and an association of NAA with social functioning suggest that NAA may be an indicator of disease severity. The lack of significant mean difference in NAA between the two groups suggests that there is no marked neuronal loss in the dorsolateral prefrontal region in schizophrenia. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:63 / 71
页数:9
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