Cannon T D, Huttunen M O, Lonnqvist J, Tuulio-Henriksson A, Pirkola T, Glahn D, Finkelstein J, Hietanen M, Kaprio J, Koskenvuo M
Department of Psychology, UCLA, 90095, USA.
Am J Hum Genet. 2000 Aug;67(2):369-82. doi: 10.1086/303006. Epub 2000 Jul 3.
While genetic influences in schizophrenia are substantial, the disorder's molecular genetic basis remains elusive. Progress has been hindered by lack of means to detect nonpenetrant carriers of the predisposing genes and by uncertainties concerning the extent of locus heterogeneity. One approach to solving this complexity is to examine the inheritance of pathophysiological processes mediating between genotype and disease phenotype. Here we evaluate whether deficits in neurocognitive functioning covary with degree of genetic relationship with a proband in the unaffected MZ and DZ co-twins of patients with schizophrenia. Twin pairs discordant for schizophrenia were recruited from a total population cohort and were compared with a demographically balanced sample of control twin pairs, on a comprehensive neuropsychological test battery. The following four neuropsychological functions contributed uniquely to the discrimination of degree of genetic loading for schizophrenia and, when combined, were more highly correlated within MZ pairs than within DZ pairs, in both discordant and control twins: spatial working memory (i.e., remembering a sequence of spatial locations over a brief delay), divided attention (i.e., simultaneous performance of a counting and visual-search task), intrusions during recall of a word list (i.e., "remembering" nonlist items), and choice reaction time to visual targets. Together with evidence from human and animal studies of mediation of these functions by partially distinct brain systems, our findings suggest that there are multiple independently inherited dimensions of neural deficit in schizophrenia and encourage a search for genes contributing to quantitative variation in discrete aspects of disease liability. On tests of verbal and visual episodic memory, but not on the liability-related measures, patients were more impaired than their own MZ co-twins, suggesting a preferential impact of nongenetic influences on long-term memory systems.
虽然精神分裂症受遗传因素的影响很大,但其分子遗传学基础仍不清楚。缺乏检测易感基因非显性携带者的方法以及基因座异质性程度的不确定性阻碍了这方面的研究进展。解决这一复杂性问题的一种方法是研究介导基因型和疾病表型之间的病理生理过程的遗传方式。在此,我们评估了精神分裂症患者未患病的同卵双生子(MZ)和异卵双生子(DZ)中,神经认知功能缺陷是否与先证者的遗传关系程度相关。从总体人群队列中招募了精神分裂症不一致的双生子对,并与人口统计学上平衡的对照双生子对样本进行比较,进行全面的神经心理测试。以下四种神经心理功能对区分精神分裂症的遗传负荷程度有独特作用,并且在不一致和对照双生子对中,当组合在一起时,MZ对中的相关性高于DZ对:空间工作记忆(即短时间延迟后记住一系列空间位置)、分散注意力(即同时执行计数和视觉搜索任务)、单词列表回忆中的侵入(即“记住”非列表项目)以及对视觉目标的选择反应时间。结合来自人类和动物研究的证据,表明这些功能由部分不同的脑系统介导,我们的研究结果表明,精神分裂症存在多个独立遗传的神经缺陷维度,并鼓励寻找导致疾病易感性离散方面数量变异的基因。在言语和视觉情景记忆测试中,但在与易感性相关的测量中并非如此,患者比他们自己的MZ同卵双生子受损更严重,这表明非遗传因素对长期记忆系统有优先影响。