Department of Psychology, University of Hawaii at Manoa, Honolulu, Hawaii.
Early Interv Psychiatry. 2020 Jun;14(3):321-329. doi: 10.1111/eip.12856. Epub 2019 Jul 4.
Greater attention is being paid to early detection and identification of individuals who are at high risk of developing psychosis. One area of interest is the particular content types of psychotic-like experiences (PLEs), which can be thought of as attenuated, non-clinical positive symptoms (eg, feeling perplexed by reality). Previous research has examined content of PLEs in clinical high-risk samples. The current study aimed to build upon these findings by analysing content in a psychometrically determined high-risk sample.
One hundred fifty-three undergraduates with scores greater than 1.96 SDs above the mean on a measure of schizotypy symptoms participated in a semi-structured interview for the assessment of prodromal syndromes. Each interview was transcribed verbatim and content of PLEs was rated according to the Content of Attenuated Positive Symptoms scale.
Frequencies of content items in the psychometric high-risk sample were similar to those found in a clinical high-risk sample. Multiple regression analyses revealed that certain content items were more predictive of decreased global functioning and increased positive symptom severity.
Content items that were associated with worse outcomes may be cause for greater concern if endorsed by individuals presenting for treatment. Future research should examine content of PLEs in a longitudinal design to determine whether particular items could predict subsequent conversion to a schizophrenia-spectrum disorder.
越来越多的人开始关注那些有发展为精神病风险的个体的早期检测和识别。一个感兴趣的领域是精神病样体验(PLE)的特定内容类型,可以将其视为减弱的非临床阳性症状(例如,对现实感到困惑)。先前的研究已经检查了临床高风险样本中的 PLE 内容。本研究旨在通过分析心理测量确定的高风险样本中的内容来进一步研究这些发现。
153 名本科生的精神分裂症症状得分高于平均水平 1.96 个标准差以上,参加了一项用于评估前驱症状的半结构化访谈。每次访谈都逐字记录,并根据减弱的阳性症状量表对 PLE 的内容进行评分。
心理测量高风险样本中的内容项目频率与临床高风险样本中的相似。多元回归分析表明,某些内容项目与降低整体功能和增加阳性症状严重程度的相关性更高。
如果个体接受治疗时出现了这些与更差结果相关的内容项目,可能需要引起更大的关注。未来的研究应该在纵向设计中检查 PLE 的内容,以确定特定项目是否可以预测随后发展为精神分裂症谱系障碍。