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The Silent Side of the Spectrum: Schizotypy and the Schizotaxic Self

机译:频谱的寂静面:精神分裂症和精神分裂性自我

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摘要

The identification of individuals carrying unexpressed genetic liability to schizophrenia is crucial for both etiological research and clinical risk stratification. Subclinical psychopathological features detectable in the nonpsychotic part of the schizophrenia spectrum could improve the delineation of informative vulnerability phenotypes. Inspired by Meehl's schizotaxia-schizotypy heuristic model, we tested anomalous subjective experiences (self-disorders, SDs) as a candidate vulnerability phenotype in a sample of nonpsychotic, genetically high-risk subjects. A total of 218 unaffected members of 6 extended multiplex families (assessed between 1989 and 1999 during the Copenhagen Schizophrenia Linkage Study) were stratified into 4 groups of increasing psychopathological expressivity: no mental illness (NMI), no mental illness with schizotypal traits (NMI-ST), personality disorders not fulfilling other personality disorders (OPDs), and schizotypal personality disorder (SPD). We tested the distribution of SDs among the subgroups, the effect of SDs on the risk of belonging to the different subgroups, and the effect of experimental grouping and concomitant psychopathology (ie, negative symptoms (NSs) and subpsychotic formal thought disorder [FTD]) on the chances of experiencing SDs. SDs distribution followed an incremental pattern from NMI to SPD. SDs were associated with a markedly increased risk of NMI-ST, OPDs, or SPD. The odds of SDs increased as a function of the diagnostic category assignment, independently of sociodemographics and concomitant subclinical psychopathology (NSs and FTD). The results support SDs as an expression of schizotaxic vulnerability and indicate a multidimensional model of schizotypy—characterized by SDs, NSs, FTD—as a promising heuristic construct to address liability phenotypes in genetically high-risk studies.
机译:鉴定携带未表达的精神分裂症遗传责任的个体对于病因学研究和临床风险分层均至关重要。在精神分裂症谱系的非精神病性部分可检测到的亚临床心理病理特征可改善信息性易损性表型的描述。受到Meehl的精神分裂症-精神分裂症启发式模型的启发,我们在非精神病性,遗传性高风险受试者的样本中测试了异常主观体验(自我障碍,SD)作为候选脆弱性表型。总共218个未受影响的成员来自6个延伸的多重家庭(在1989年至1999年之间在哥本哈根精神分裂症连锁研究中进行评估),分为4组,其精神病理学表达水平不断提高:无精神疾病(NMI),无精神分裂症特征的精神疾病(NMI- ST),无法满足其他人格障碍(OPD)的人格障碍和精神分裂型人格障碍(SPD)。我们测试了SD在各亚组之间的分布,SD对属于不同亚组的风险的影响以及实验分组和伴随的心理病理学(即阴性症状(NSs)和亚精神病性正式思想障碍[FTD])的影响体验SD的机会。 SD的分布遵循从NMI到SPD的增量模式。 SD与NMI-ST,OPD或SPD的风险显着增加有关。与社会人口统计学和伴随的亚临床心理病理学(NSs和FTD)无关,SDs的机率随诊断类别分配的增加而增加。结果支持SDs作为一种分裂性脆弱性的表达,并指出了一个由SDs,NSs,FTD表征的精神分裂症的多维模型,作为解决遗传性高风险研究中责任表型的一种有前途的启发式结构。

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  • 来源
    《Schizophrenia Bulletin》 |2011年第5期|p.1017-1026|共10页
  • 作者

    Josef Parnas;

  • 作者单位

    Danish National Research Foundation: Center for Subjectivity Research, University of Copenhagen, Njalsgade 140–142, Building 25, 2300 Copenhagen S, Denmark;

    tel: +45-35-32-86-86, fax: +45-35-32-86-81, e-mail:;

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  • 入库时间 2022-08-18 01:07:20

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