Laboratory of Neuro Imaging, Department of Neurology, UCLA School of Medicine, Los Angeles, CA 90095-1769, USA.
Neuroimage. 2011 Jun 15;56(4):1875-91. doi: 10.1016/j.neuroimage.2011.03.077. Epub 2011 Apr 8.
Imaging traits provide a powerful and biologically relevant substrate to examine the influence of genetics on the brain. Interest in genome-wide, brain-wide search for influential genetic variants is growing, but has mainly focused on univariate, SNP-based association tests. Moving to gene-based multivariate statistics, we can test the combined effect of multiple genetic variants in a single test statistic. Multivariate models can reduce the number of statistical tests in gene-wide or genome-wide scans and may discover gene effects undetectable with SNP-based methods. Here we present a gene-based method for associating the joint effect of single nucleotide polymorphisms (SNPs) in 18,044 genes across 31,662 voxels of the whole brain in 731 elderly subjects (mean age: 75.56±6.82SD years; 430 males) from the Alzheimer's Disease Neuroimaging Initiative (ADNI). Structural MRI scans were analyzed using tensor-based morphometry (TBM) to compute 3D maps of regional brain volume differences compared to an average template image based on healthy elderly subjects. Using the voxel-level volume difference values as the phenotype, we selected the most significantly associated gene (out of 18,044) at each voxel across the brain. No genes identified were significant after correction for multiple comparisons, but several known candidates were re-identified, as were other genes highly relevant to brain function. GAB2, which has been previously associated with late-onset AD, was identified as the top gene in this study, suggesting the validity of the approach. This multivariate, gene-based voxelwise association study offers a novel framework to detect genetic influences on the brain.
成像特征为研究遗传对大脑的影响提供了一个强大且与生物学相关的基础。人们对全基因组、全脑范围内寻找有影响力的遗传变异的兴趣日益浓厚,但主要集中在单变量、基于 SNP 的关联测试上。采用基于基因的多元统计方法,我们可以在单个统计检验中测试多个遗传变异的综合效应。多元模型可以减少基因或全基因组扫描中的统计检验次数,并可能发现基于 SNP 的方法无法检测到的基因效应。在这里,我们提出了一种基于基因的方法,用于关联 18044 个基因中 SNP 的联合效应,这些 SNP 分布在 731 名老年受试者(平均年龄:75.56±6.82SD 岁;430 名男性)的整个大脑的 31662 个体素中,这些受试者来自阿尔茨海默病神经影像学倡议 (ADNI)。使用基于张量的形态测量学 (TBM) 分析结构 MRI 扫描,以计算与基于健康老年人的平均模板图像相比的区域脑体积差异的 3D 图谱。使用体素水平的体积差异值作为表型,我们在整个大脑的每个体素中选择最显著相关的基因(在 18044 个基因中)。经过多重比较校正后,没有基因被确定为显著,但重新识别了一些已知的候选基因,以及与大脑功能高度相关的其他基因。GAB2 先前与迟发性 AD 相关,在本研究中被确定为排名最高的基因,表明该方法的有效性。这种多元、基于基因的体素关联研究为检测遗传对大脑的影响提供了一个新的框架。