Rebelo Miguel Ângelo, Gómez Carlos, Gomes Iva, Poza Jesús, Martins Sandra, Maturana-Candelas Aarón, Ruiz-Gómez Saúl J, Durães Luis, Sousa Patrícia, Figueruelo Manuel, Rodríguez María, Pita Carmen, Arenas Miguel, Álvarez Luis, Hornero Roberto, Pinto Nádia, Lopes Alexandra M
IPATIMUP-Instituto de Patologia e Imunologia Molecular da Universidade do Porto, 4200-135 Porto, Portugal.
I3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.
Brain Sci. 2020 Nov 18;10(11):870. doi: 10.3390/brainsci10110870.
Brain waves, measured by electroencephalography (EEG), are a powerful tool in the investigation of neurophysiological traits and a noninvasive and cost-effective alternative in the diagnostic of some neurological diseases. In order to identify novel Quantitative Trait Loci (QTLs) for brain wave relative power (RP), we collected resting state EEG data in five frequency bands (δ, θ, α, β1, and β2) and genome-wide data in a cohort of 105 patients with late onset Alzheimer's disease (LOAD), 41 individuals with mild cognitive impairment and 45 controls from Iberia, correcting for disease status. One novel association was found with an interesting candidate for a role in brain wave biology, (C-type lectin domain family 16), with a variant at this locus passing the adjusted genome-wide significance threshold after Bonferroni correction. This finding reinforces the importance of immune regulation in brain function. Additionally, at a significance cutoff value of 5 × 10, 18 independent association signals were detected. These signals comprise brain expression Quantitative Loci (eQTLs) in caudate basal ganglia, spinal cord, anterior cingulate cortex and hypothalamus, as well as chromatin interactions in adult and fetal cortex, neural progenitor cells and hippocampus. Moreover, in the set of genes showing signals of association with brain wave RP in our dataset, there is an overrepresentation of loci previously associated with neurological traits and pathologies, evidencing the pleiotropy of the genetic variation modulating brain function.
通过脑电图(EEG)测量的脑电波是研究神经生理特征的有力工具,也是诊断某些神经系统疾病的一种非侵入性且经济高效的替代方法。为了确定脑电波相对功率(RP)的新数量性状基因座(QTL),我们收集了105名晚发性阿尔茨海默病(LOAD)患者、41名轻度认知障碍个体和45名来自伊比利亚的对照的静息态EEG数据,涵盖五个频段(δ、θ、α、β1和β2)以及全基因组数据,并对疾病状态进行了校正。发现了一个与脑电波生物学中一个有趣的候选基因(C型凝集素结构域家族16)的新关联,该位点的一个变体在Bonferroni校正后超过了调整后的全基因组显著性阈值。这一发现强化了免疫调节在脑功能中的重要性。此外,在显著性截止值为5×10时,检测到18个独立的关联信号。这些信号包括尾状基底神经节、脊髓、前扣带回皮质和下丘脑的脑表达数量基因座(eQTL),以及成人和胎儿皮质、神经祖细胞和海马体中的染色质相互作用。此外,在我们的数据集中显示与脑电波RP有关联信号的基因集中,先前与神经特征和病理学相关的基因座存在过度表达,这证明了调节脑功能的遗传变异具有多效性。