颞叶癫痫患者小脑功能梯度和分子遗传机制的变化:横断面和纵向功能磁共振成像研究。

IF 2.4 3区 医学 Q3 NEUROSCIENCES
Shujun Su, Qin Zhou, Xuemei Chen, Bailing Qin, Yuting Sun, Lu Qin, Chuan Yong Qu, Jinou Zheng
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引用次数: 0

摘要

目的探讨颞叶癫痫(TLE)患者小脑功能梯度的横断面和纵向变化特征,并探讨其分子遗传机制。本研究包括横断面和纵向两个阶段。横断面研究纳入115例TLE患者和75例健康对照(hc),采用静息状态功能磁共振成像(rs-fMRI)分析小脑功能连接梯度;纵向研究随访29例TLE患者和29例hc患者,评估4年(44.24±16.64个月)期间小脑功能连通性梯度的变化。来自Allen人脑图谱的基因表达数据被用来分析梯度变化差异与基因表达的关系。(1) TLE患者和hc患者均表现出典型的功能性小脑梯度模式。(2)横断面分析显示,TLE患者小脑主梯度范围缩小,默认模式网络(DMN)梯度值明显升高。(3)纵向分析显示,TLE患者的小脑DMN梯度在基线时(BL)初始异常;随着疾病进展,DMN趋于稳定。(4)共鉴定出151个与梯度差异相关的基因,氧化石墨烯富集分析主要涉及胞吞作用、突触结构、代谢和离子通道。蛋白相互作用网络分析发现WASF1、RAC1和MTG1是关键枢纽基因。本研究首次通过功能磁共振成像梯度分析为TLE患者小脑功能梯度的动态变化及其潜在的分子相关性提供了初步证据,为认识TLE的神经可塑性提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in Cerebellar Functional Gradients and Molecular Genetic Mechanisms in Patients with Temporal Lobe Epilepsy: a cross-sectional and Longitudinal Functional Magnetic Resonance Imaging Study.

To investigate the characteristics of cross-sectional and longitudinal changes in cerebellar functional gradients in patients with temporal lobe epilepsy (TLE) and to explore the underlying molecular genetic mechanisms.This study included both cross-sectional and longitudinal phases. The cross-sectional study included 115 TLE patients and 75 healthy controls (HCs) and analyzed the cerebellar functional connectivity gradient using resting-state functional magnetic resonance imaging (rs-fMRI); the longitudinal study followed 29 TLE patients and 29 HCs and assessed the changes in the cerebellar functional connectivity gradient over a four-year period (44.24 ± 16.64 months). Gene expression data from the Allen Human Brain Atlas were used to analyze the association of differences in gradient changes with gene expression. (1) Both TLE patients and HCs showed typical functional cerebellar gradient patterns. (2) Cross-sectional analyses revealed that TLE patients had a contracted range of main cerebellar gradients and significantly higher gradient values in the default mode network (DMN). (3) Longitudinal analyses showed that cerebellar DMN gradients were initially abnormal in TLE patients at baseline(BL); with disease progression, the DMN stabilized. (4) 151 genes associated with gradient differences were identified, and GO enrichment analysis mainly involved endocytosis, synaptic structure, metabolism, and ion channels. Protein interaction network analysis identified WASF1, RAC1 and MTG1 as key hub genes. This study provides initial evidence of dynamic changes in cerebellar functional gradients and their potential molecular correlates in TLE patients for the first time by functional magnetic resonance imaging gradient analysis, providing a new perspective for understanding the neuroplasticity of TLE.

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来源期刊
Cerebellum
Cerebellum 医学-神经科学
CiteScore
6.40
自引率
14.30%
发文量
150
审稿时长
4-8 weeks
期刊介绍: Official publication of the Society for Research on the Cerebellum devoted to genetics of cerebellar ataxias, role of cerebellum in motor control and cognitive function, and amid an ageing population, diseases associated with cerebellar dysfunction. The Cerebellum is a central source for the latest developments in fundamental neurosciences including molecular and cellular biology; behavioural neurosciences and neurochemistry; genetics; fundamental and clinical neurophysiology; neurology and neuropathology; cognition and neuroimaging. The Cerebellum benefits neuroscientists in molecular and cellular biology; neurophysiologists; researchers in neurotransmission; neurologists; radiologists; paediatricians; neuropsychologists; students of neurology and psychiatry and others.
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