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分析 KCNH2 和 CACNA1C 精神分裂症风险基因对听觉Oddball 任务中 EEG 功能网络调制的影响。

Analysis of KCNH2 and CACNA1C schizophrenia risk genes on EEG functional network modulation during an auditory odd-ball task.

机构信息

Psychiatry Department, School of Medicine, University of Valladolid, Av. Ramón y Cajal, 7, 47005, Valladolid, Spain.

FIDMAG Germanes Hospitalàries Research Foundation, Carrer Del Dr. Antoni Pujadas, 38 Sant Boi De Llobregat, 08830, Barcelona, Spain.

出版信息

Eur Arch Psychiatry Clin Neurosci. 2020 Jun;270(4):433-442. doi: 10.1007/s00406-018-0977-0. Epub 2019 Jan 3.

Abstract

A deficit in task-related functional connectivity modulation from electroencephalogram (EEG) has been described in schizophrenia. The use of measures of neuronal connectivity as an intermediate phenotype may allow identifying genetic factors involved in these deficits, and therefore, establishing underlying pathophysiological mechanisms. Genes involved in neuronal excitability and previously associated with the risk for schizophrenia may be adequate candidates in relation to functional connectivity alterations in schizophrenia. The objective was to study the association of two genes of voltage-gated ion channels (CACNA1C and KCNH2) with the functional modulation of the cortical networks measured with EEG and graph-theory parameter during a cognitive task, both in individuals with schizophrenia and healthy controls. Both CACNA1C (rs1006737) and KCNH2 (rs3800779) were genotyped in 101 controls and 50 schizophrenia patients. Small-world index (SW) was calculated from EEG recorded during an odd-ball task in two different temporal windows (pre-stimulus and response). Modulation was defined as the difference in SW between both windows. Genetic, group and their interaction effects on SW in the pre-stimulus window and in modulation were evaluated using ANOVA. The CACNA1C genotype was not associated with SW properties. KCNH2 was significantly associated with SW modulation. Healthy subjects showed a positive SW modulation irrespective of the KCNH2 genotype, whereas within patients allele-related differences were observed. Patients carrying the KCNH2 risk allele (A) presented a negative SW modulation and non-carriers showed SW modulation similar to the healthy subjects. Our data suggest that KCNH2 genotype contributes to the efficient modulation of brain electrophysiological activity during a cognitive task in schizophrenia patients.

摘要

研究表明,精神分裂症患者存在与任务相关的脑功能连接调制缺陷。使用神经元连接测量作为中间表型,可以识别参与这些缺陷的遗传因素,并因此确定潜在的病理生理机制。涉及神经元兴奋性的基因与精神分裂症的风险相关,可能是与精神分裂症脑功能连接改变相关的合适候选基因。本研究旨在研究电压门控离子通道(CACNA1C 和 KCNH2)的两个基因与 EEG 测量的皮质网络功能调制以及认知任务期间的图论参数之间的关联,包括精神分裂症患者和健康对照组。在 101 名对照者和 50 名精神分裂症患者中对 CACNA1C(rs1006737)和 KCNH2(rs3800779)进行了基因分型。在两种不同的时间窗口(刺激前和反应期)的Odd-ball 任务中记录 EEG,计算小世界指数(SW)。调制定义为两个窗口之间 SW 的差异。使用 ANOVA 评估遗传、组和它们之间的交互效应对刺激前窗口中的 SW 和调制的影响。CACNA1C 基因型与 SW 特性无关。KCNH2 与 SW 调制显著相关。健康受试者无论 KCNH2 基因型如何,均表现出正的 SW 调制,而在患者中观察到等位基因相关差异。携带 KCNH2 风险等位基因(A)的患者表现出负的 SW 调制,而非携带者表现出与健康受试者相似的 SW 调制。我们的数据表明,KCNH2 基因型有助于精神分裂症患者在认知任务期间大脑电生理活动的有效调制。

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