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Clinical Utility and Lifespan Profiling of Neurological Soft Signs in Schizophrenia Spectrum Disorders

机译:精神分裂症频谱障碍的神经软体征的临床效用和寿命分析

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摘要

Neurological soft signs (NSSs) bear the promise for early detection of schizophrenia spectrum disorders. Nonetheless, the sensitivity and specificity of NSSs in the psychosis continuum remains a topic of controversy. It is also unknown how NSSs reveal neurodevelopmental abnormality in schizophrenia. We investigated the effect sizes of NSSs in differentiating individuals with schizophrenia spectrum disorders from individuals with other psychiatric conditions and from covariate-matched healthy subjects. We also investigated the partitioned age-related variations of NSSs in both schizophrenia and healthy individuals. NSSs were assessed by the abridged version of the Cambridge Neurological Inventory (CNI) in 3105 participants, consisting of healthy individuals (n =1577), unaffected first-degree relatives of schizophrenia patients (n = 155), individuals with schizotypal personality disorder (n = 256), schizophrenia patients (n = 738), and other psychiatric patients (n = 379). Exact matching and propensity score matching procedures were performed to control for covariates. Multiple regression was used to partition age-related variations. Individuals along the schizophrenia continuum showed elevated levels of NSSs, with moderate effect sizes, in contrast to other psychiatric patients who had minimal NSSs, as well as matched healthy controls. Furthermore, the age-and-NSS relationship in schizophrenia patients was represented by a flat but overall elevated pattern, in contrast to a U-shaped pattern in healthy individuals. In sum, NSSs capture a moderate portion of psychosis proneness with reasonable specificity. Lifespan profiling reveals an abnormal developmental trajectory of NSSs in schizophrenia patients, which supports the endophenotype hypothesis of NSSs by associating it with the neurodevelopmental model of schizophrenia.
机译:神经系统软体征(NSSs)有望早日发现精神分裂症频谱疾病。但是,精神病连续体中NSS的敏感性和特异性仍然是一个有争议的话题。还不清楚NSSs如何揭示精神分裂症的神经发育异常。我们调查了精神分裂症谱系障碍患者与其他精神病患者和协变量匹配健康受试者的区别,NSSs的作用大小。我们还研究了精神分裂症和健康个体中NSSs的与年龄相关的分区性变异。 NSS是由3105名参与者组成的剑桥神经病学目录(CNI)的简化版评估的,包括健康个体(n = 1577),精神分裂症患者的未受影响的一级亲属(n = 155),患有精神分裂型人格障碍的个体(n = 256),精神分裂症患者(n = 738)和其他精神病患者(n = 379)。进行精确匹配和倾向得分匹配程序以控制协变量。多元回归被用来划分与年龄有关的变异。与其他精神病患者的NSS最少,以及相匹配的健康对照相比,精神分裂症连续体中的个体显示出较高的NSS水平,且效应大小适中。此外,精神分裂症患者的年龄与NSS关系以平坦但总体升高的模式表示,与健康个体中的U形模式相反。总而言之,NSSs具有合理特异性的中等程度的精神病倾向。寿命谱分析揭示了精神分裂症患者中NSS的异常发育轨迹,通过将其与精神分裂症的神经发育模型相关联来支持NSS的内表型假说。

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