Neuroimaging and Treatment Evidence for Clinical Staging in Psychotic Disorders: From the At-Risk Mental State to Chronic Schizophrenia

被引:77
作者
Wood, Stephen J. [1 ,3 ]
Yung, Alison R. [2 ]
McGorry, Patrick D. [2 ]
Pantelis, Christos [1 ]
机构
[1] Univ Melbourne, Dept Psychiat, Melbourne Neuropsychiat Ctr, Melbourne, Vic, Australia
[2] Univ Melbourne, Orygen Youth Hlth Res Ctr, Melbourne, Vic, Australia
[3] Univ Birmingham, Sch Psychol, Edgbaston, England
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
Clinical staging; diagnosis; neuroimaging; psychosis; schizophrenia; treatment; ULTRA-HIGH-RISK; MAGNETIC-RESONANCE-SPECTROSCOPY; ETHYL-EICOSAPENTAENOIC ACID; COGNITIVE-BEHAVIORAL THERAPY; RANDOMIZED CONTROLLED-TRIAL; SUPERIOR TEMPORAL GYRUS; FOLLOW-UP; 1ST-EPISODE SCHIZOPHRENIA; PSYCHIATRIC-DISORDERS; EPISODE SCHIZOPHRENIA;
D O I
10.1016/j.biopsych.2011.05.034
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A new approach to understanding severe mental disorders such as schizophrenia is to adopt a clinical staging model. Such a model defines the extent of the illness such that earlier and milder phenomena are distinguished from later, more impairing features. Specifically, a clinical staging model makes three key predictions. First, pathologic measures should be more abnormal in more severe stages. Second, patients who progress between the stages should show change in these same pathologic measures. Finally, treatment should be more effective in the earlier stages, as well as more benign. In this article, we review the evidence for these three predictions from studies of psychotic disorders, with a focus on neuroimaging data. For all three, the balance of evidence supports the predictions of the staging model. However, there are a number of alternative explanations for these findings, including the effects of medication and symptom heterogeneity.
引用
收藏
页码:619 / 625
页数:7
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