K.G. Jebsen Centre for Psychosis Research, Norwegian Centre for Mental Disorders Research (NORMENT), Department of Clinical Science, University of Bergen, Bergen, Norway; Dr. Einar Martens Research Group for Biological Psychiatry, Center for Medical Genetics and Molecular Medicine, Haukeland University Hospital, Bergen, Norway; K.G. Jebsen Centre for Psychosis Research, Norwegian Centre for Mental Disorders Research (NORMENT), Department of Clinical Science, University of Bergen, Bergen, Norway.
K.G. Jebsen Centre for Psychosis Research, Norwegian Centre For Mental Disorders Research (NORMENT), Division of Mental Health and Addiction, Oslo University Hospital & Institute of Clinical Medicine, University of Oslo, Oslo, Norway; Department of Psychology, University of Oslo, Oslo N-0317, Norway.
Psychiatry Res. 2014 Apr 30;222(1-2):60-6. doi: 10.1016/j.pscychresns.2014.02.009. Epub 2014 Feb 22.
The rs1344706 single nucleotide polymorphism within intron 2 of the ZNF804A gene is strongly associated with schizophrenia and bipolar disorder. This variant has also been associated in some studies with a range of cognitive and neuroimaging phenotypes, but several studies have reported no effect on the same phenotypes in other samples. Here, we genotyped 670 healthy adult Norwegian subjects and 1753 healthy adult Swedish subjects for rs1344706, and tested for associations with cognitive phenotypes including general intellectual abilities, memory functions and cognitive inhibition. We also tested whether rs1344706 is associated with white matter microstructural properties using diffusion tensor imaging (DTI) data from 250 to 340 of the Norwegian and Swedish subjects, respectively. Whole-brain voxel-wise statistical modeling of the effect of the ZNF804A variant on two DTI indices, fractional anisotropy (FA) and radial diffusivity (RD), was performed using tract-based spatial statistics (TBSS), and commonly reported effect sizes were calculated within several large-scale white matter pathways based on neuroanatomical atlases. No significant associations were found between rs1344706 and the cognitive traits or white matter microstructure. We conclude that the rs1344706 SNP has no significant effect on these phenotypes in our two reasonably powered samples.
锌指蛋白 804A 基因(ZNF804A)内含子 2 内的 rs1344706 单核苷酸多态性与精神分裂症和双相情感障碍强烈相关。该变体在一些研究中还与一系列认知和神经影像学表型相关,但几项研究报告在其他样本中对相同表型没有影响。在这里,我们对 670 名健康的挪威成年受试者和 1753 名健康的瑞典成年受试者进行了 rs1344706 基因分型,并测试了其与认知表型的关联,包括一般智力、记忆功能和认知抑制。我们还使用分别来自 250 至 340 名挪威和瑞典受试者的弥散张量成像 (DTI) 数据,测试了 rs1344706 是否与白质微观结构特性相关。使用基于纤维束的空间统计学 (TBSS) 对 ZNF804A 变体对两个 DTI 指数(各向异性分数 (FA) 和径向扩散率 (RD))的影响进行全脑体素统计建模,并根据神经解剖图谱在几个大规模白质通路上计算了常见的报告效应量。rs1344706 与认知特征或白质微观结构之间没有发现显著关联。我们得出结论,在我们两个具有合理效力的样本中,rs1344706 SNP 对这些表型没有显著影响。