Department of Psychology, University of New Mexico, Albuquerque, New Mexico, USA.
Biol Psychiatry. 2013 Mar 15;73(6):540-5. doi: 10.1016/j.biopsych.2012.10.013. Epub 2012 Dec 11.
General cognitive ability is usually lower in individuals with schizophrenia, partly due to genetic influences. However, the specific genetic features related to general cognitive ability are poorly understood. Individual variation in a specific type of mutation, uncommon genetic deletions, has recently been linked with both general cognitive ability and risk for schizophrenia.
We derived measures of the aggregate number of "uncommon" deletions (i.e., those occurring in 3% or less of our combined samples) and the total number of base pairs affected by these deletions in individuals with schizophrenia (n = 79) and healthy control subjects (n = 110) and related each measure to the first principal component of a large battery of cognitive tests, a common technique for characterizing general cognitive ability. These two measures of mutation load were also evaluated for relationships with total brain gray matter, white matter, and lateral ventricle volume.
The groups did not differ on genetic variables. Multivariate general linear models revealed a group (control subjects vs. patients) × uncommon deletion number interaction, such that the latter variable was associated with lower general cognitive ability and larger ventricles in patients but not control subjects.
These data suggest that aggregate uncommon deletion burden moderates central features of the schizophrenia phenotype.
一般认知能力在精神分裂症患者中通常较低,部分原因是遗传影响。然而,与一般认知能力相关的具体遗传特征还知之甚少。最近,一种特定类型的突变——罕见的遗传缺失——个体变异与一般认知能力和精神分裂症风险都有关联。
我们在精神分裂症患者(n=79)和健康对照受试者(n=110)中得出了罕见缺失(即发生在我们合并样本的 3%或更少的个体中)的总数和这些缺失影响的碱基对总数的综合指标,并将每个指标与大量认知测试的第一主成分相关联,这是一种描述一般认知能力的常用技术。还评估了这两种突变负荷指标与总脑灰质、白质和侧脑室体积的关系。
两组在遗传变量上没有差异。多变量一般线性模型显示出组(对照受试者与患者)×罕见缺失数量的相互作用,表明后者变量与患者的一般认知能力降低和脑室增大有关,但与对照受试者无关。
这些数据表明,罕见缺失负担的总和调节了精神分裂症表型的中枢特征。