Development of Liability Syndromes for Schizophrenia: Where Did They Come From and Where Are They Going?

被引:2
|
作者
Stone, William S. [1 ]
Giuliano, Anthony J. [1 ]
机构
[1] Harvard Univ, Sch Med, Massachusetts Mental Hlth Ctr, Div Beth Israel Deaconess Med Ctr,Dept Psychiat, Boston, MA 02115 USA
关键词
schizotaxia; schizophrenia liability; prodrome; neuropsychology; negative symptoms; FINNISH ADOPTIVE FAMILY; CLINICAL HIGH-RISK; GENOTYPE-ENVIRONMENT INTERACTION; ULTRA-HIGH RISK; FOLLOW-UP; OBSTETRIC COMPLICATIONS; NONPSYCHOTIC RELATIVES; INTERRATER RELIABILITY; GENETIC VULNERABILITY; ENDOPHENOTYPE CONCEPT;
D O I
10.1002/ajmg.b.32185
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Three decades after Paul Meehl proposed the term schizotaxia to describe a conceptual framework for understanding the liability to schizophrenia, Ming Tsuang et al. at Harvard University reformulated the concept as a clinical syndrome with provisional research criteria. The reformulated view relied heavily on more recent data showing that many non-psychotic, un-medicated biological relatives of individuals with schizophrenia showed difficulties in cognitive and other clinical functions that resembled those seen in their ill relatives. The reformulation raised questions about both whether and when liability could be assessed validly in the absence of psychosis, and about the extent to which symptoms of liability are reversible. Both questions bear on the larger issue of early intervention in schizophrenia. This article reviews the efforts of Tsuang et al. to conceptualize and validate schizotaxia as one such syndrome of liability. Towards this end, liability is considered first more generally as an outcome of interactive genetic and environmental factors. Liability is then considered in the context of endophenotypes as a concept that is both broader and is potentially more specific (and predictive) than many DSM or ICD diagnostic symptoms. Liability syndromes are then considered in the context of their proximity to illness, first by reviewing prodromal syndromes (which are more proximal), and then by considering schizotaxia, which, as it is currently formulated, is pre-prodromal and, therefore, less proximal. Finally, challenges to validation and future directions for research are considered. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:687 / 697
页数:11
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