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双生子人群中,异常突显与精神病性体验的相关性,以及作为修饰因素的遗传易感性。

The association between aberrant salience and psychotic experiences in general population twins, and genetic vulnerability as a modifier.

机构信息

Department of Psychiatry and Neuropsychology, School of Mental Health and Neuroscience (MHeNS), Maastricht University Medical Centre, Maastricht, the Netherlands.

Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands.

出版信息

BMC Psychiatry. 2024 Oct 26;24(1):736. doi: 10.1186/s12888-024-06176-2.

Abstract

BACKGROUND

Previous studies assessing the hypothesis that the construct of 'aberrant salience' is associated with psychosis and psychotic symptoms showed conflicting results. For this reason, the association between measures to index aberrant salience and subclinical psychotic symptoms in a general population sample was analysed. In addition, genetic vulnerability was added to the analysis as a modifier to test the hypothesis that modification by genetic vulnerability may explain variability in the results.

METHODS

The TwinssCan project obtained data from general population twins (N = 887). CAPE (Community Assessment of Psychic Experience) scores were used to index psychotic experiences. Aberrant salience was assessed with white noise task and ambiguous situations task.

RESULTS

Measures of aberrant salience were not associated with psychotic experiences, nor was there evidence for an interaction with genetic predisposition in this association (Z = 1.08, p = 0.282).

CONCLUSIONS

Various studies including the present could not replicate the association between aberrant salience and psychotic experiences in general population samples. The conflicting findings might be explained by moderation by genetic vulnerability, but results are inconsistent. If there was evidence for a main effect or interaction, this was in the positive symptom scale only. On the other hand, the association was more robust in so-called 'ultra-high risk' patients and first episode psychosis patients. Thus, this association may represent a state-dependent association, present only at the more severe end of the psychosis spectrum.

摘要

背景

先前评估“异常突显”结构与精神病和精神病症状相关假设的研究结果存在矛盾。因此,本研究分析了一般人群样本中异常突显指标与亚临床精神病症状之间的关联。此外,还将遗传易感性纳入分析,作为修饰因子,以检验遗传易感性修饰可能解释结果变异性的假设。

方法

TwinssCan 项目从一般人群双胞胎(N=887)中获取数据。CAPE(社区心理体验评估)评分用于评估精神病体验。使用白噪声任务和模糊情境任务评估异常突显。

结果

异常突显指标与精神病体验无关,也没有证据表明遗传易感性在这种关联中存在交互作用(Z=1.08,p=0.282)。

结论

包括本研究在内的各种研究都无法复制异常突显与一般人群样本中精神病体验之间的关联。相互矛盾的结果可能是遗传易感性的修饰作用所致,但结果不一致。如果存在主要效应或交互作用的证据,则仅见于阳性症状量表。另一方面,在所谓的“超高危”患者和首发精神病患者中,这种关联更为稳健。因此,这种关联可能代表一种与状态相关的关联,仅存在于精神病谱的更严重端。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e9/11515186/690353603fd7/12888_2024_6176_Fig1_HTML.jpg

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