期刊
ARCHIVES OF GENERAL PSYCHIATRY
卷 67, 期 6, 页码 578-588出版社
AMER MEDICAL ASSOC
DOI: 10.1001/archgenpsychiatry.2010.66
关键词
-
类别
资金
- National Institute of Mental Health [R18 MH 43518, U01 MH081928, P50 M11080272]
- [U01 MH066134]
- [RO1 MH60720]
- [K24 MH76191]
- [R01 MH65079]
- [K05MH01654]
- [U01 MH066069]
- [P50 MH064065]
- [RO1MH062066]
- [5 U01 MH081988]
- [U01 MH74356]
- [U01 MH082022]
- [R41 MH083436]
- [RO1 MH061523]
- NATIONAL INSTITUTE OF MENTAL HEALTH [U01MH074356, R41MH083436, U01MH081944, U01MH066134, U01MH066069, P50MH064065, R37MH043518, U01MH082004, U01MH082022, R01MH065079, R01MH043518, K05MH001654, U01MH081988, R01MH060720, R01MH061523, U01MH081928, R01MH062066, K24MH076191, P50MH080272] Funding Source: NIH RePORTER
Context: Early detection and prospective evaluation of clinical high-risk (CHR) individuals who may develop schizophrenia or other psychotic disorders is critical for predicting psychosis onset and for testing preventive interventions. Objectives: To elucidate the neuropsychology of the CHR syndrome, to determine the association of neuropsychological function with conversion to psychosis and family history of psychosis, and to examine whether baseline neuropsychological functioning predicts subsequent psychosis. Design: Longitudinal study with 2 1/2 years of follow-up. Setting: Eight centers participating in the North American Prodrome Longitudinal Study. Participants: Three hundred four prospectively identified CHR individuals meeting Structured Interview for Prodromal Syndromes criteria, 52 non-CHR persons with a family history of psychosis in first- or second-degree relatives (family high-risk group), and 193 normal controls with neither a family history of psychosis nor a CHR syndrome, all of whom underwent baseline neuropsychological evaluations. Main Outcome Measures: A neurocognitive composite score, 8 individual neuropsychological measures, an IQ estimate, and high-risk status. Results: Global (composite) neuropsychological functioning was comparably impaired in the CHR and family high-risk groups compared with controls, but profiles differed significantly between groups. Neuropsychological functioning in the CHR group was significantly lower in persons who progressed to psychosis than in those who did not and was worst in the subgroup with a family history of psychosis. Tests of processing speed and verbal learning and memory were most sensitive in discriminating CHR individuals from controls, although reductions were less severe than in established schizophrenia. Neuropsychological functioning did not contribute uniquely to the prediction of psychosis beyond clinical criteria, but worse verbal memory predicted more rapid conversion. Conclusions: These findings document that CHR individuals have significant neuropsychological difficulties, particularly those who later develop psychosis. This dysfunction is generally of moderate severity but less than in first-episode schizophrenia, suggesting that further decline may occur after baseline CHR assessment.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据