Zong Xiaofen, He Changchun, Huang Xinyue, Xiao Jinming, Li Lei, Li Meiling, Yao Tao, Hu Maolin, Liu Zhongchun, Duan Xujun, Zheng Junjie
Department of Psychiatry, Renmin Hospital of Wuhan University, Wuhan, China.
The High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, University of Electronic Science and Technology of China, Chengdu, China.
Front Neurosci. 2022 May 9;16:853186. doi: 10.3389/fnins.2022.853186. eCollection 2022.
Volumetric alterations of subcortical structures as predictors of antipsychotic treatment response have been previously corroborated, but less is known about whether their morphological covariance relates to treatment outcome and is driven by gene expression and epigenetic modifications.
Subcortical volumetric covariance was analyzed by using baseline T1-weighted magnetic resonance imaging (MRI) in 38 healthy controls and 38 drug-naïve first-episode schizophrenia patients. Patients were treated with 8-week risperidone monotherapy and divided into responder and non-responder groups according to the Remission in Schizophrenia Working Group (RSWG). We utilized partial least squares (PLS) regression to examine the spatial associations between gene expression of subcortical structures from a publicly available transcriptomic dataset and between-group variances of structural covariance. The peripheral DNA methylation (DNAm) status of a gene of interest (GOI), overlapping between genes detected in the PLS and 108 schizophrenia candidate gene loci previously reported, was examined in parallel with MRI scanning.
In the psychotic symptom dimension, non-responders had a higher baseline structural covariance in the putamen-hippocampus-pallidum-accumbens pathway compared with responders. For disorganized symptoms, significant differences in baseline structural covariant connections were found in the putamen-hippocampus-pallidum-thalamus circuit between the two subgroups. The imaging variances related to psychotic symptom response were spatially related to the expression of genes enriched in neurobiological processes and dopaminergic pathways. The DNAm of GOI demonstrated significant associations with patients' improvement of psychotic symptoms.
Baseline subcortical structural covariance and peripheral DNAm may relate to antipsychotic treatment response. Phenotypic variations in subcortical connectome related to psychotic symptom response may be transcriptomically and epigenetically underlaid. This study defines a roadmap for future studies investigating multimodal imaging epigenetic biomarkers for treatment response in schizophrenia.
先前已证实皮质下结构的体积改变可作为抗精神病药物治疗反应的预测指标,但对于它们的形态协方差是否与治疗结果相关以及是否由基因表达和表观遗传修饰驱动,我们了解得较少。
使用基线T1加权磁共振成像(MRI)对38名健康对照者和38名未服用过药物的首发精神分裂症患者的皮质下体积协方差进行分析。患者接受为期8周的利培酮单药治疗,并根据精神分裂症缓解工作组(RSWG)的标准分为反应者和无反应者组。我们利用偏最小二乘(PLS)回归来研究来自公开可用转录组数据集的皮质下结构基因表达与结构协方差组间差异之间的空间关联。在进行MRI扫描的同时,平行检测了一个感兴趣基因(GOI)的外周DNA甲基化(DNAm)状态,该基因在PLS检测到的基因与先前报道的108个精神分裂症候选基因位点之间存在重叠。
在精神病性症状维度上,与反应者相比,无反应者在壳核-海马-苍白球-伏隔核通路中的基线结构协方差更高。对于紊乱症状,在两个亚组之间的壳核-海马-苍白球-丘脑回路中发现基线结构协变连接存在显著差异。与精神病性症状反应相关的成像差异在空间上与神经生物学过程和多巴胺能通路中富集的基因表达相关。GOI的DNAm与患者精神病性症状的改善显著相关。
基线皮质下结构协方差和外周DNAm可能与抗精神病药物治疗反应相关。与精神病性症状反应相关的皮质下连接组表型变异可能在转录组和表观遗传层面有其基础。本研究为未来研究精神分裂症治疗反应的多模态成像表观遗传生物标志物定义了路线图。