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本文引用的文献

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Neurocognitive functioning in subjects at risk for a first episode of psychosis compared with first- and multiple-episode schizophrenia.首次发作精神病风险受试者与首次发作及多次发作精神分裂症患者的神经认知功能比较
J Clin Exp Neuropsychol. 2006 Nov;28(8):1388-407. doi: 10.1080/13803390500434425.
2
A longitudinal study of neurocognitive function in individuals at-risk for psychosis.一项针对有精神病风险个体的神经认知功能的纵向研究。
Schizophr Res. 2006 Dec;88(1-3):26-35. doi: 10.1016/j.schres.2006.06.041. Epub 2006 Aug 22.
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Neurocognitive performance and functional disability in the psychosis prodrome.精神病前驱期的神经认知表现与功能残疾
Schizophr Res. 2006 May;84(1):100-11. doi: 10.1016/j.schres.2006.02.005. Epub 2006 Mar 24.
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Intellectual decline in schizophrenia: evidence from a prospective birth cohort 28 year follow-up study.精神分裂症患者的智力衰退:来自一项前瞻性出生队列28年随访研究的证据。
J Clin Exp Neuropsychol. 2006 Feb;28(2):225-42. doi: 10.1080/13803390500360471.
5
Generalized and specific neurocognitive deficits in prodromal schizophrenia.前驱期精神分裂症的广泛性和特异性神经认知缺陷。
Biol Psychiatry. 2006 May 1;59(9):863-71. doi: 10.1016/j.biopsych.2005.09.005. Epub 2005 Dec 1.
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Spatial working memory deficits in adolescents at clinical high risk for schizophrenia.临床高危精神分裂症青少年的空间工作记忆缺陷
Schizophr Res. 2006 Jan 31;81(2-3):211-5. doi: 10.1016/j.schres.2005.09.019.
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Long-term neurocognitive effects of olanzapine or low-dose haloperidol in first-episode psychosis.奥氮平或低剂量氟哌啶醇对首发精神病的长期神经认知影响。
Biol Psychiatry. 2006 Jan 15;59(2):97-105. doi: 10.1016/j.biopsych.2005.06.022. Epub 2005 Sep 2.
8
Sustained attention in young people at high risk of psychosis does not predict transition to psychosis.在精神病高风险的年轻人中,持续注意力并不能预测其是否会发展为精神病。
Schizophr Res. 2005 Nov 1;79(1):127-36. doi: 10.1016/j.schres.2005.06.023.
9
The psychosis prodrome in adolescent patients viewed through the lens of DSM-IV.从《精神疾病诊断与统计手册第四版》(DSM-IV)的视角看青少年患者的精神病前驱症状。
J Child Adolesc Psychopharmacol. 2005 Jun;15(3):434-51. doi: 10.1089/cap.2005.15.434.
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Course of cognitive functioning in first episode schizophrenia spectrum disorders.首发精神分裂症谱系障碍的认知功能进程
Expert Rev Neurother. 2004 Jan;4(1):61-8. doi: 10.1586/14737175.4.1.61.

处于精神病超高风险个体的神经认知与社会功能进程。

The course of neurocognition and social functioning in individuals at ultra high risk for psychosis.

作者信息

Niendam Tara A, Bearden Carrie E, Zinberg Jamie, Johnson Jennifer K, O'Brien Mary, Cannon Tyrone D

机构信息

Department of Psychology, University of California, Los Angeles, 1285 Franz Hall, Box 951563, Los Angeles, CA 90095-1563, USA.

出版信息

Schizophr Bull. 2007 May;33(3):772-81. doi: 10.1093/schbul/sbm020. Epub 2007 Apr 9.

DOI:10.1093/schbul/sbm020
PMID:17420177
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2526130/
Abstract

OBJECTIVE

This study evaluates longitudinal neuropsychological performance and its association with clinical symptomatology and psychosocial outcome in individuals identified as ultra high risk (UHR) for psychosis.

METHODS

Thirty-five UHR individuals completed neurocognitive, clinical, and social/role functioning assessments at baseline and, on average, 8.3 months later.

RESULTS

UHR subjects showed significant cognitive deficits at baseline and 2 distinct profiles of cognitive change over time. On average, 50% demonstrated improvement in social and role functioning over the follow-up period, while the other half showed either stability or decline in functioning. Functional improvement was associated with improved processing speed and visual memory, as well as improvement in clinical symptoms over the follow-up period. In contrast, patients who did not improve functionally showed stable clinical symptoms and cognitive performance over time.

CONCLUSIONS

Although the degree of neurocognitive deficit at baseline in UHR patients does not predict psychosocial outcome, the course of neurocognitive change over the first 8 months of follow-up does differentiate patients with good and poor functional outcomes.

摘要

目的

本研究评估被确定为精神病超高风险(UHR)个体的纵向神经心理学表现及其与临床症状和社会心理结局的关联。

方法

35名UHR个体在基线时以及平均8.3个月后完成了神经认知、临床和社会/角色功能评估。

结果

UHR受试者在基线时表现出显著的认知缺陷,且随着时间推移有2种不同的认知变化模式。平均而言,50%的受试者在随访期间社会和角色功能有所改善,而另一半受试者的功能则保持稳定或下降。功能改善与处理速度和视觉记忆的改善以及随访期间临床症状的改善相关。相比之下,功能未改善的患者随着时间推移临床症状和认知表现保持稳定。

结论

尽管UHR患者基线时的神经认知缺陷程度不能预测社会心理结局,但随访前8个月的神经认知变化过程确实能区分功能结局良好和不良的患者。