Clinical Utility and Lifespan Profiling of Neurological Soft Signs in Schizophrenia Spectrum Disorders
Chan, Raymond C. K.1; Xie, Weizhen2; Geng, Fu-lei1,3; Wang, Ya1; Lui, Simon S. Y.1,3,4; Wang, Chuan-yue5,6; Yu, Xin7,8,9; Cheung, Eric F. C.4; Rosenthal, Robert2
刊名SCHIZOPHRENIA BULLETIN
2016-05-01
卷号42期号:3页码:560-570
关键词neurological soft sign schizophrenia spectrum disorders lifespan profiling psychopathology endophenotype
ISSN号0586-7614
英文摘要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.
WOS标题词Science & Technology ; Life Sciences & Biomedicine
类目[WOS]Psychiatry
研究领域[WOS]Psychiatry
关键词[WOS]OBSESSIVE-COMPULSIVE DISORDER ; MINI-MENTAL-STATE ; PROPENSITY SCORE ; 1ST-EPISODE SCHIZOPHRENIA ; BRAIN-DEVELOPMENT ; MATCHING METHODS ; CAUSAL ; ENDOPHENOTYPES ; MULTIVARIATE ; METAANALYSIS
收录类别SCI ; SSCI
语种英语
WOS记录号WOS:000376402000009
内容类型期刊论文
源URL[http://ir.psych.ac.cn/handle/311026/19998]  
专题心理研究所_中国科学院心理健康重点实验室
作者单位1.Chinese Acad Sci, Inst Psychol, Key Lab Mental Hlth, Neuropsychol & Appl Cognit Neurosci Lab, Beijing 100101, Peoples R China
2.Univ Calif Riverside, Dept Psychol, Riverside, CA 92521 USA
3.Univ Chinese Acad Sci, Beijing, Peoples R China
4.Castle Peak Hosp, Hong Kong, Hong Kong, Peoples R China
5.Capital Med Univ, Beijing Anding Hosp, Dept Psychiat, Beijing Key Lab Mental Disorders, Beijing, Peoples R China
6.Capital Med Univ, Beijing Inst Brain Disorders, Ctr Schizophrenia, Minist Sci & Technol,Lab Brain Disorders, Beijing, Peoples R China
7.Peking Univ, Hosp 6, Beijing 100871, Peoples R China
8.Peking Univ, Inst Mental Hlth, Beijing 100871, Peoples R China
9.Peking Univ, Minist Hlth, Key Lab Mental Hlth, Beijing 100871, Peoples R China
推荐引用方式
GB/T 7714
Chan, Raymond C. K.,Xie, Weizhen,Geng, Fu-lei,et al. Clinical Utility and Lifespan Profiling of Neurological Soft Signs in Schizophrenia Spectrum Disorders[J]. SCHIZOPHRENIA BULLETIN,2016,42(3):560-570.
APA Chan, Raymond C. K..,Xie, Weizhen.,Geng, Fu-lei.,Wang, Ya.,Lui, Simon S. Y..,...&Rosenthal, Robert.(2016).Clinical Utility and Lifespan Profiling of Neurological Soft Signs in Schizophrenia Spectrum Disorders.SCHIZOPHRENIA BULLETIN,42(3),560-570.
MLA Chan, Raymond C. K.,et al."Clinical Utility and Lifespan Profiling of Neurological Soft Signs in Schizophrenia Spectrum Disorders".SCHIZOPHRENIA BULLETIN 42.3(2016):560-570.
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