Department of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Department of Computer Science, University College London, London, UK.
Neuroimage Clin. 2018;20:1026-1036. doi: 10.1016/j.nicl.2018.10.008. Epub 2018 Oct 9.
Psychiatric illnesses are complex and polygenic. They are associated with widespread alterations in the brain, which are partly influenced by genetic factors. There have been some attempts to relate polygenic risk scores (PRS) - a measure of the overall genetic risk an individual carries for a disorder - to brain structure using univariate methods. However, PRS are likely associated with distributed and covarying effects across the brain. We therefore used multivariate machine learning in this proof-of-principle study to investigate associations between brain structure and PRS for four psychiatric disorders; attention deficit-hyperactivity disorder (ADHD), autism, bipolar disorder and schizophrenia. The sample included 213 individuals comprising patients with depression (69), bipolar disorder (33), and healthy controls (111). The five psychiatric PRSs were calculated based on summary data from the Psychiatric Genomics Consortium. T1-weighted magnetic resonance images were obtained and voxel-based morphometry was implemented in SPM12. Multivariate relevance vector regression was implemented in the Pattern Recognition for Neuroimaging Toolbox (PRoNTo). Across the whole sample, a multivariate pattern of grey matter significantly predicted the PRS for autism (r = 0.20, p = 0.03; MSE = 4.20 × 10, p = 0.02). For the schizophrenia PRS, the MSE was significant (MSE = 1.30 × 10, p = 0.02) although the correlation was not (r = 0.15, p = 0.06). These results lend support to the hypothesis that polygenic liability for autism and schizophrenia is associated with widespread changes in grey matter concentrations. These associations were seen in individuals not affected by these disorders, indicating that this is not driven by the expression of the disease, but by the genetic risk captured by the PRSs.
精神疾病是复杂的多基因疾病。它们与大脑的广泛改变有关,而这些改变部分受到遗传因素的影响。已经有人试图使用单变量方法将多基因风险评分(PRS)——个体对一种疾病携带的总体遗传风险的衡量标准——与大脑结构联系起来。然而,PRS 可能与大脑中分布和共变的效应有关。因此,在这项原理验证研究中,我们使用多变量机器学习来研究四种精神障碍(注意缺陷多动障碍(ADHD)、自闭症、双相情感障碍和精神分裂症)的大脑结构与 PRS 之间的关联。样本包括 213 名个体,包括抑郁症患者(69 名)、双相情感障碍患者(33 名)和健康对照组(111 名)。五个精神 PRS 是根据精神病基因组学联合会的汇总数据计算的。获得 T1 加权磁共振图像,并在 SPM12 中实施基于体素的形态测量学。模式识别神经影像学工具箱(PRoNTo)中实施了多变量相关性向量回归。在整个样本中,灰质的多变量模式显著预测了自闭症 PRS(r=0.20,p=0.03;MSE=4.20×10,p=0.02)。对于精神分裂症 PRS,MSE 是显著的(MSE=1.30×10,p=0.02),尽管相关性不显著(r=0.15,p=0.06)。这些结果支持这样一种假设,即自闭症和精神分裂症的多基因易感性与灰质浓度的广泛变化有关。这些关联在不受这些疾病影响的个体中可见,表明这不是由疾病的表达驱动的,而是由 PRS 捕获的遗传风险驱动的。