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精神分裂症和双相情感障碍的基因?对精神疾病分类学的影响。

Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology.

作者信息

Craddock Nick, O'Donovan Michael C, Owen Michael J

机构信息

Department of Psychological Medicine, Henry Wellcome Building, Wales School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, UK.

出版信息

Schizophr Bull. 2006 Jan;32(1):9-16. doi: 10.1093/schbul/sbj033. Epub 2005 Nov 30.

Abstract

It has been conventional for psychiatric research, including the search for predisposing genes, to proceed under the assumption that schizophrenia and bipolar disorder are separate disease entities with different underlying etiologies. These represent Emil Kraepelin's traditional dichotomous classification of the so-called "functional" psychoses and form the basis of modern diagnostic practice. However, findings emerging from many fields of psychiatric research do not fit well with this model. In particular, the pattern of findings emerging from genetic studies shows increasing evidence for an overlap in genetic susceptibility across the traditional classification categories-including association findings at DAOA(G72), DTNBP1 (dysbindin), COMT, BDNF, DISC1, and NRG1. The emerging evidence suggests the possibility of relatively specific relationships between genotype and psychopathology. For example, DISC1 and NRG1 may confer susceptibility to a form of illness with mixed features of schizophrenia and mania. The elucidation of genotype-phenotype relationships is at an early stage, but current findings highlight the need to consider alternative approaches to classification and conceptualization for psychiatric research rather than continuing to rely heavily on the traditional Kraepelinian dichotomy. As psychosis susceptibility genes are identified and characterized over the next few years, this will have a major impact on our understanding of disease pathophysiology and will lead to changes in classification and the clinical practice of psychiatry.

摘要

一直以来,包括寻找易感基因在内的精神病学研究惯例是,在精神分裂症和双相情感障碍是具有不同潜在病因的独立疾病实体这一假设下进行。这些代表了埃米尔·克雷佩林对所谓“功能性”精神病的传统二分法分类,并构成了现代诊断实践的基础。然而,精神病学研究诸多领域出现的研究结果并不完全符合这一模型。特别是,遗传学研究中出现的研究结果模式显示,越来越多的证据表明,传统分类类别之间在遗传易感性方面存在重叠——包括在DAOA(G72)、DTNBP1(dysbindin)、COMT、BDNF、DISC1和NRG1等基因座上的关联研究结果。新出现的证据表明,基因型与精神病理学之间可能存在相对特定的关系。例如,DISC1和NRG1可能使人易患具有精神分裂症和躁狂症混合特征的某种疾病形式。基因型-表型关系的阐明尚处于早期阶段,但当前的研究结果凸显出,精神病学研究需要考虑采用替代的分类和概念化方法,而不是继续严重依赖传统的克雷佩林二分法。随着未来几年精神病易感性基因被识别和表征,这将对我们对疾病病理生理学的理解产生重大影响,并将导致分类和精神病临床实践的改变。

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