Keefe Richard S E, Perkins Diana O, Gu Hongbin, Zipursky Robert B, Christensen Bruce K, Lieberman Jeffery A
Department of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, NC 27710, USA.
Schizophr Res. 2006 Dec;88(1-3):26-35. doi: 10.1016/j.schres.2006.06.041. Epub 2006 Aug 22.
Clinically defined prodromal diagnostic criteria identify at-risk individuals with a 35-40% likelihood of developing a psychotic disorder within a year. The time course and predictive value of cognitive deficits in the development of psychosis has not been established.
A comprehensive neurocognitive battery and clinical assessments were administered to 37 subjects meeting Criteria of Prodromal States (COPS) criteria for being at risk for psychosis, and two comparison groups: 59 first episode and 47 healthy subjects. Subjects were also evaluated at 6-month and 1-year follow-up periods. Primary analyses used a neurocognitive composite score derived from individual neurocognitive measures, including measures of vigilance, verbal memory, working memory, and processing speed.
At-risk subjects performed more poorly than healthy subjects (t=2.93, P=0.01), but better than first episode subjects (t=4.72, p<0.0001). At-risk subjects were particularly impaired on measures of vigilance and processing speed. Cognitive composite scores were significantly lower in at-risk subjects who progressed to psychosis (N=11; z=-1.2), while those at-risk subjects who did not progress to psychosis (N=17) performed better (z=-0.5), and not significantly different from controls. Poor CPT performance combined with better WAIS-R digit symbol performance predicted progression to psychosis. Severity of neurocognitive deficits was not related to duration of prodrome or to time to development of psychosis and neurocognitive function improved in all subjects except those who progressed to psychosis.
Neurocognitive impairment emerges early in the course of psychotic illness. Performance on tests of neurocognition may prove to be an early risk predictor for subsequent development of psychotic disorders.
临床定义的前驱期诊断标准可识别出有风险的个体,这些个体在一年内患精神病性障碍的可能性为35%-40%。认知缺陷在精神病发展过程中的时间进程和预测价值尚未确定。
对37名符合前驱期状态标准(COPS)的有精神病风险的受试者,以及两个对照组:59名首发患者和47名健康受试者,进行了全面的神经认知测试和临床评估。受试者还在6个月和1年的随访期接受评估。主要分析使用了从个体神经认知测量得出的神经认知综合评分,包括警觉性、言语记忆、工作记忆和处理速度的测量。
有风险的受试者表现比健康受试者差(t=2.93,P=0.01),但比首发患者好(t=4.72,p<0.0001)。有风险的受试者在警觉性和处理速度测量方面尤其受损。进展为精神病的有风险受试者(N=11;z=-1.2)的认知综合评分显著更低,而未进展为精神病的有风险受试者(N=17)表现更好(z=-0.5),且与对照组无显著差异。连续性能测试(CPT)表现差且韦氏成人智力量表修订版(WAIS-R)数字符号表现较好可预测进展为精神病。神经认知缺陷的严重程度与前驱期持续时间或精神病发展时间无关,除进展为精神病的受试者外,所有受试者的神经认知功能均有改善。
神经认知损害在精神病性疾病过程中早期出现。神经认知测试表现可能被证明是后续精神病性障碍发展的早期风险预测指标。