4.6 Article

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

期刊

SCHIZOPHRENIA BULLETIN
卷 42, 期 3, 页码 560-570

出版社

OXFORD UNIV PRESS
DOI: 10.1093/schbul/sbv196

关键词

neurological soft sign; schizophrenia spectrum disorders; lifespan profiling; psychopathology; endophenotype

资金

  1. National Science Fund China [81088001]
  2. Beijing Training Project for the Leading Talents in S T [Z151100000315020]
  3. National Basic Research Programme (973 Programme) [2007CB512302]
  4. Knowledge Innovation Project of the Chinese Academy of Sciences [KSCX2-EW-J-8]
  5. key Laboratory of Mental Health, Institute of Psychology
  6. CAS/SAFEA International Partnership Programme for Creative Research Teams [Y2CX131003]

向作者/读者索取更多资源

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.

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