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首页> 外文期刊>International Journal of Molecular Sciences >GeneAnalytics Pathway Analysis and Genetic Overlap among Autism Spectrum Disorder, Bipolar Disorder and Schizophrenia
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GeneAnalytics Pathway Analysis and Genetic Overlap among Autism Spectrum Disorder, Bipolar Disorder and Schizophrenia

机译:自闭症谱系障碍,双相情感障碍和精神分裂症的基因分析途径分析和遗传重叠

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Bipolar disorder (BPD) and schizophrenia (SCH) show similar neuropsychiatric behavioral disturbances, including impaired social interaction and communication, seen in autism spectrum disorder (ASD) with multiple overlapping genetic and environmental influences implicated in risk and course of illness. GeneAnalytics software was used for pathway analysis and genetic profiling to characterize common susceptibility genes obtained from published lists for ASD (792 genes), BPD (290 genes) and SCH (560 genes). Rank scores were derived from the number and nature of overlapping genes, gene-disease association, tissue specificity and gene functions subdivided into categories (e.g., diseases, tissues or functional pathways). Twenty-three genes were common to all three disorders and mapped to nine biological Superpathways including Circadian entrainment (10 genes, score = 37.0), Amphetamine addiction (five genes, score = 24.2), and Sudden infant death syndrome (six genes, score = 24.1). Brain tissues included the medulla oblongata (11 genes, score = 2.1), thalamus (10 genes, score = 2.0) and hypothalamus (nine genes, score = 2.0) with six common genes ( BDNF , DRD2 , CHRNA7 , HTR2A , SLC6A3 , and TPH2 ). Overlapping genes impacted dopamine and serotonin homeostasis and signal transduction pathways, impacting mood, behavior and physical activity level. Converging effects on pathways governing circadian rhythms support a core etiological relationship between neuropsychiatric illnesses and sleep disruption with hypoxia and central brain stem dysfunction.
机译:躁郁症(BPD)和精神分裂症(SCH)表现出类似的神经精神行为障碍,包括自闭症谱系障碍(ASD)中出现的社交互动和沟通障碍,遗传和环境影响多重重叠,涉及疾病的风险和病程。使用GeneAnalytics软件进行途径分析和基因分析,以表征从已发表的ASD(792个基因),BPD(290个基因)和SCH(560个基因)列表中获得的常见易感基因。等级评分是根据重叠基因的数量和性质,基因-疾病关联,组织特异性和基因功能划分的类别(例如疾病,组织或功能途径)得出的。这三种疾病共有23个基因,并映射到9个生物超途径,包括昼夜节律(10个基因,得分= 37.0),苯丙胺成瘾(五个基因,得分= 24.2)和婴儿猝死综合征(六个基因,得分= 24.1)。脑组织包括延髓(11个基因,得分= 2.1),丘脑(10个基因,得分= 2.0)和下丘脑(9个基因,得分= 2.0)以及六个常见基因(BDNF,DRD2,CHRNA7,HTR2A,SLC6A3和TPH2)。重叠的基因影响多巴胺和5-羟色胺的稳态和信号转导途径,影响情绪,行为和身体活动水平。在控制昼夜节律的途径上的趋同效应支持神经精神疾病与睡眠不足与缺氧和中枢脑干功能障碍之间的核心病因学关系。

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