Wood Stephen J, Brewer Warrick J, Koutsouradis Penny, Phillips Lisa J, Francey Shona M, Proffitt Tina M, Yung Alison R, Jackson Henry J, McGorry Patrick D, Pantelis Christos
Melbourne Neuropsychiatry Centre, Department of Psychiatry, University of Melbourne, c/o National Neuroscience Facility, 161 Barry Street, Carlton South, VIC 3053 Australia.
Br J Psychiatry Suppl. 2007 Dec;51:s52-7. doi: 10.1192/bjp.191.51.s52.
The origin of cognitive impairments in psychotic disorders is still unclear. Although some deficits are apparent prior to the onset of frank illness, it is unknown if they progress.
To investigate whether cognitive function declined over the transition to psychosis in a group of ultra-high risk individuals.
Participants consisted of two groups: controls (n=17) and individuals at ultra-high risk for development of psychosis (n=16). Seven of the latter group later developed psychosis. Neuropsychological testing was conducted at baseline and again after at least a 12-month interval.
Both the Visual Reproduction sub-test of the Wechsler Memory Scale-Revised and Trail-Making Test B showed a decline over the follow-up period that was specific to the group who became psychotic. In addition, both high-risk groups showed a decline in digit span performance. No other task showed significant change over time.
These preliminary data suggest that as psychosis develops there may be a specific decline in visual memory and attentional set-shifting, reflecting impairments in efficient organisation of visual stimuli. This may be caused by either the illness itself or treatment with antipsychotic medication.
精神障碍中认知损害的起源仍不明确。尽管在明显发病之前就存在一些缺陷,但它们是否会进展尚不清楚。
调查一组超高风险个体在向精神病转变过程中认知功能是否下降。
参与者分为两组:对照组(n = 17)和有超高风险发展为精神病的个体(n = 16)。后一组中有7人后来发展为精神病。在基线时以及至少间隔12个月后再次进行神经心理学测试。
韦氏记忆量表修订版的视觉再现子测试和连线测验B在随访期间均显示出下降,这是特定于发展为精神病的那组人的。此外,两个高风险组的数字广度表现均有所下降。没有其他任务随时间显示出显著变化。
这些初步数据表明,随着精神病的发展,视觉记忆和注意力转换可能会出现特定下降,反映出视觉刺激有效组织方面的损害。这可能是由疾病本身或抗精神病药物治疗引起的。