Cell-type-specific genes associated with cortical structural abnormalities in pediatric bipolar disorder.

Psychoradiology Pub Date : 2022-09-23 eCollection Date: 2022-06-01 DOI:10.1093/psyrad/kkac009
Wenkun Lei, Qian Xiao, Chun Wang, Weijia Gao, Yiwen Xiao, Yingliang Dai, Guangming Lu, Linyan Su, Yuan Zhong
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Abstract

Background: Pediatric bipolar disorder (PBD) has been proven to be related to abnormal brain structural connectivity, but how the abnormalities in PBD correlate with gene expression is debated.

Objective: This study aims at identification of cell-type-specific gene modules based on cortical structural differences in PBD.

Methods: Morphometric similarity networks (MSN) were computed as a marker of interareal cortical connectivity based on MRI data from 102 participants (59 patients and 43 controls). Partial least squares (PLS) regression was used to calculate MSN differences related to transcriptomic data in AHBA. The biological processes and cortical cell types associated with this gene expression profile were determined by gene enrichment tools.

Results: MSN analysis results demonstrated differences of cortical structure between individuals diagnosed with PBD and healthy control participants. MSN differences were spatially correlated with the PBD-related weighted genes. The weighted genes were enriched for "trans-synaptic signaling" and "regulation of ion transport", and showed significant specific expression in excitatory and inhibitory neurons.

Conclusions: This study identified the genes that contributed to structural network aberrations in PBD. It was found that transcriptional changes of excitatory and inhibitory neurons might be associated with abnormal brain structural connectivity in PBD.

与小儿躁郁症皮质结构异常相关的细胞类型特异基因。
背景:小儿双相情感障碍(PBD)已被证实与大脑结构连接异常有关,但PBD的异常如何与基因表达相关还存在争议:本研究旨在根据PBD的皮层结构差异鉴定细胞类型特异性基因模块:方法:根据102名参与者(59名患者和43名对照组)的核磁共振成像数据,计算形态计量相似性网络(MSN),作为区域间皮质连通性的标记。使用偏最小二乘法(PLS)回归计算与 AHBA 转录组数据相关的 MSN 差异。通过基因富集工具确定了与该基因表达谱相关的生物过程和皮层细胞类型:结果:MSN分析结果表明,被诊断为PBD的患者与健康对照组患者的大脑皮层结构存在差异。MSN 差异与 PBD 相关加权基因在空间上相关。加权基因富集于 "跨突触信号转导 "和 "离子转运调节",并在兴奋性和抑制性神经元中表现出显著的特异性表达:本研究确定了导致 PBD 结构网络畸变的基因。结论:本研究确定了导致 PBD 结构网络异常的基因,发现兴奋性和抑制性神经元的转录变化可能与 PBD 的大脑结构连接异常有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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