Neuroscience and Mental Health Research Institute (NMHI), College of Biomedical and Life Sciences, Cardiff University, Maindy Road CF24 4HQ, Cardiff, Wales, UK.
Cardiff University Brain Research Imaging Centre (CUBRIC), School of Psychology, College of Biomedical and Life Sciences, Cardiff University, Maindy Road CF24 4HQ, Cardiff, Wales, UK.
Cereb Cortex. 2023 Mar 10;33(6):2997-3011. doi: 10.1093/cercor/bhac256.
Research studies based on tractography have revealed a prominent reduction of asymmetry in some key white-matter tracts in schizophrenia (SCZ). However, we know little about the influence of common genetic risk factors for SCZ on the efficiency of routing on structural brain networks (SBNs). Here, we use a novel recall-by-genotype approach, where we sample young adults from a population-based cohort (ALSPAC:N genotyped = 8,365) based on their burden of common SCZ risk alleles as defined by polygenic risk score (PRS). We compared 181 individuals at extremes of low (N = 91) or high (N = 90) SCZ-PRS under a robust diffusion MRI-based graph theoretical SBN framework. We applied a semi-metric analysis revealing higher SMR values for the high SCZ-PRS group compared with the low SCZ-PRS group in the left hemisphere. Furthermore, a hemispheric asymmetry index showed a higher leftward preponderance of indirect connections for the high SCZ-PRS group compared with the low SCZ-PRS group (PFDR < 0.05). These findings might indicate less efficient structural connectivity in the higher genetic risk group. This is the first study in a population-based sample that reveals differences in the efficiency of SBNs associated with common genetic risk variants for SCZ.
基于束路径追踪的研究表明,精神分裂症(SCZ)患者的一些关键白质束的不对称性明显减少。然而,我们对 SCZ 的常见遗传风险因素对结构脑网络(SBN)路由效率的影响知之甚少。在这里,我们使用了一种新的基于基因型召回的方法,根据多基因风险评分(PRS)定义的常见 SCZ 风险等位基因的负担,从基于人群的队列(ALSPAC:N 基因分型= 8365)中抽样年轻成年人。我们比较了在稳健的基于扩散磁共振成像的图理论 SBN 框架下处于 SCZ-PRS 低值(N=91)或高值(N=90)极端的 181 个人。我们应用了一种半度量分析,结果显示高 SCZ-PRS 组的 SMR 值高于低 SCZ-PRS 组的 SMR 值,这一结果在左半球更为明显。此外,半球不对称指数显示,高 SCZ-PRS 组的间接连接左偏优势高于低 SCZ-PRS 组(PFDR<0.05)。这些发现可能表明在具有更高遗传风险的组中,结构连接的效率较低。这是在基于人群的样本中首次揭示与 SCZ 常见遗传风险变异相关的 SBN 效率差异的研究。