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多基因风险评分衍生的皮质下连接介导注意缺陷/多动障碍的诊断。

Polygenic Risk Score-Derived Subcortical Connectivity Mediates Attention-Deficit/Hyperactivity Disorder Diagnosis.

机构信息

Department of Behavioral Neuroscience, Oregon Health & Science University, Portland, Oregon.

Division of Bioinformatics & Computational Biology, Oregon Health & Science University, Portland, Oregon; Knight Cancer Institute, Oregon Health & Science University, Portland, Oregon.

出版信息

Biol Psychiatry Cogn Neurosci Neuroimaging. 2020 Mar;5(3):330-341. doi: 10.1016/j.bpsc.2019.11.014. Epub 2019 Dec 13.

Abstract

BACKGROUND

Attention-deficit/hyperactivity disorder (ADHD) has substantial heritability, and a recent large-scale investigation has identified common genome-wide significant loci associated with increased risk for ADHD. Along the same lines, many studies using noninvasive neuroimaging have identified differences in brain functional connectivity in children with ADHD. We attempted to bridge these studies to identify differences in functional connectivity associated with common genetic risk for ADHD using polygenic risk score (PRS).

METHODS

We computed ADHD PRSs for all participants in our sample (N = 315, children 7-13 years of age, 196 with ADHD and 119 unaffected comparison children) using ADHD data from the Psychiatric Genomics Consortium as a discovery set. Magnetic resonance imaging was used to evaluate resting-state functional connectivity of targeted subcortical structures.

RESULTS

The functional connectivity between 2 region pairs demonstrated a significant correlation to PRS: right caudate-parietal cortex and nucleus accumbens-occipital cortex. Connectivity between these areas, in addition to being correlated with PRS, was correlated with ADHD status. The connection between the caudate and the parietal region acted as a statistical suppressor, such that when it was included in a path model, the association between PRS and ADHD status was enhanced.

CONCLUSIONS

Our results suggest that functional connectivity to certain subcortical brain regions is directly altered by genetic variants, and certain cortico-subcortical connections may modulate ADHD-related genetic effects.

摘要

背景

注意缺陷多动障碍(ADHD)具有显著的遗传性,最近一项大规模的研究已经确定了与 ADHD 风险增加相关的常见全基因组显著位点。同样,许多使用非侵入性神经影像学的研究已经在 ADHD 儿童中发现了大脑功能连接的差异。我们试图将这些研究联系起来,使用多基因风险评分(PRS)来识别与 ADHD 常见遗传风险相关的功能连接差异。

方法

我们使用来自精神疾病基因组学联盟的 ADHD 数据作为发现集,为我们样本中的所有参与者(N=315,年龄为 7-13 岁,196 名患有 ADHD,119 名未受影响的对照儿童)计算了 ADHD PRS。磁共振成像用于评估靶向皮质下结构的静息状态功能连接。

结果

2 个区域对之间的功能连接与 PRS 呈显著相关:右侧尾状核-顶叶皮层和伏隔核-枕叶皮层。这些区域之间的连通性不仅与 PRS 相关,而且与 ADHD 状态相关。尾状核和顶叶区域之间的连接充当统计抑制器,使得当它被包含在路径模型中时,PRS 与 ADHD 状态之间的关联得到增强。

结论

我们的结果表明,某些皮质下脑区的功能连接直接受到遗传变异的影响,某些皮质下连接可能调节与 ADHD 相关的遗传效应。

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