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Associated Genetics and Connectomic Circuitry in Schizophrenia and Bipolar Disorder

机译:精神分裂症和双相情感障碍中的相关遗传学和连接组学回路

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? 2022 Society of Biological PsychiatryBackground: Schizophrenia (SCZ) and bipolar disorder (BD) are severe psychiatric conditions that can involve symptoms of psychosis and cognitive dysfunction. The 2 conditions share symptomatology and genetic etiology and are regularly hypothesized to share underlying neuropathology. Here, we examined how genetic liability to SCZ and BD shapes normative variations in brain connectivity. Methods: We examined the effect of the combined genetic liability for SCZ and BD on brain connectivity from two perspectives. First, we examined the association between polygenic scores for SCZ and BD for 19,778 healthy subjects from the UK Biobank and individual variation in brain structural connectivity reconstructed by means of diffusion weighted imaging data. Second, we conducted genome-wide association studies using genotypic and imaging data from the UK Biobank, taking SCZ-/BD-involved brain circuits as phenotypes of interest. Results: Our findings showed brain circuits of superior parietal and posterior cingulate regions to be associated with polygenic liability for SCZ and BD, circuitry that overlaps with brain networks involved in disease conditions (r = 0.239, p < .001). Genome-wide association study analysis showed 9 significant genomic loci associated with SCZ-involved circuits and 14 loci associated with BD-involved circuits. Genes related to SCZ-/BD-involved circuits were significantly enriched in gene sets previously reported in genome-wide association studies for SCZ and BD. Conclusions: Our findings suggest that polygenic liability of SCZ and BD is associated with normative individual variation in brain circuitry.
机译:?2022 生物精神病学学会背景:精神分裂症 (SCZ) 和双相情感障碍 (BD) 是严重的精神疾病,可能涉及精神病和认知功能障碍的症状。这两种疾病具有共同的症状学和遗传病因学,并且经常被假设为具有共同的潜在神经病理学。在这里,我们研究了对 SCZ 和 BD 的遗传易感性如何塑造大脑连接的规范变异。方法:我们从两个角度研究了SCZ和BD的综合遗传责任对大脑连接的影响。首先,我们检查了来自英国生物银行的 19,778 名健康受试者的 SCZ 和 BD 多基因评分与通过扩散加权成像数据重建的大脑结构连接个体差异之间的关联。其次,我们使用来自英国生物银行的基因型和成像数据进行了全基因组关联研究,将 SCZ-/BD 参与的脑回路作为感兴趣的表型。结果:我们的研究结果显示,顶上和后扣带回区域的脑回路与 SCZ 和 BD 的多基因易感性有关,这些回路与与疾病状况相关的脑网络重叠 (r = 0.239,p < .001)。全基因组关联研究分析显示,9个与SCZ相关电路相关的重要基因组位点和14个与BD相关电路相关的位点。与SCZ-/BD相关电路相关的基因在先前在SCZ和BD的全基因组关联研究中报道的基因集中显着富集。 结论:我们的研究结果表明,SCZ和BD的多基因易感性与脑回路的规范个体变异有关。

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