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Genetic Influences on Behavioral Outcomes After Childhood TBI: A Novel Systems Biology-Informed Approach

机译:遗传对儿童TBI后行为结局的影响:一种新型的系统生物学信息学方法

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摘要

Objectives: To test whether genetic associations with behavioral outcomes after early childhood traumatic brain injury (TBI) are enriched for biologic pathways underpinning neurocognitive and behavioral networks.Design: Cross-sectional evaluation of the association of genetic factors with early (~ 6 months) and long-term (~ 7 years) post-TBI behavioral outcomes. We combined systems biology and genetic association testing methodologies to identify biologic pathways associated with neurocognitive and behavior outcomes after TBI. We then evaluated whether genes/single nucleotide polymorphism (SNPs) associated with these biologic pathways were more likely to demonstrate a relationship (i.e., enrichment) with short and long-term behavioral outcomes after early childhood TBI compared to genes/SNPs not associated with these biologic pathways.Setting: Outpatient research setting.Participants:140 children, ages 3–6:11 years at time of injury, admitted for a TBI or orthopedic injury (OI).Interventions: Not Applicable.Main Outcome Measures: Child behavior checklist total problems T score.Results: Systems biology methodology identified neuronal systems and neurotransmitter signaling (Glutamate receptor, dopamine, serotonin, and calcium signaling), inflammatory response, cell death, immune systems, and brain development as important biologic pathways to neurocognitive and behavioral outcomes after TBI. At 6 months post injury, the group (TBI versus OI) by polymorphism interaction was significant when the aggregate signal from the highest ranked 40% of case gene associations was compared to the control set of genes. At ~ 7 years post injury, the selected polymorphisms had a significant main effect after controlling for injury type when the aggregate signal from the highest ranked 10% of the case genes were compared to the control set of genesConclusions: Findings demonstrate the promise of applying a genomics approach, informed by systems biology, to understanding behavioral recovery after pediatric TBI. A mixture of biologic pathways and processes are associated with behavioral recovery, specifically genes associated with cell death, inflammatory response, neurotransmitter signaling, and brain development. These results provide insights into the complex biology of TBI recovery.
机译:目的:要测试在早期儿童创伤性脑损伤(TBI)后与行为结果的遗传关联是否丰富了支持神经认知和行为网络的生物途径。设计:横断面评估遗传因素与TBI行为早期(〜6个月)和长期(〜7年)的关联。我们结合了系统生物学和遗传协会测试方法,以识别与TBI后的神经认知和行为结果相关的生物学途径。然后,我们评估了与这些生物学途径相关的基因/单核苷酸多态性(SNP)与不与这些生物学途径相关联的基因/ SNP相比,更可能表现出与儿童早期TBI后短期和长期行为结果的关系(即,丰富性)。生物学途径。设置:门诊研究设置。参与者: 140名受伤时年龄为3–6:11岁的儿童,因TBI或骨伤(OI)入院。干预措施:不适用。主要结果指标:儿童行为清单总问题T评分。结果:系统生物学方法识别出神经元系统和神经递质信号(谷氨酸受体,多巴胺,5-羟色胺和钙信号传导),炎症反应,细胞死亡,免疫系统和脑发育是TBI后获得神经认知和行为结果的重要生物学途径。在受伤后6个月,当将来自案例基因关联性最高的40%的最高信号的总信号与对照组基因进行比较时,多态性相互作用的组(TBI与OI)非常重要。在受伤后约7年,将来自病例排名最高10%的病例基因的聚集信号与对照组基因进行比较后,选定的多态性在控制损伤类型后具有重要的主要作用。结论:研究结果证明了应用基因组学方法(根据系统生物学知识)来理解小儿TBI后的行为恢复的希望。生物学途径和过程的混合与行为恢复有关,特别是与细胞死亡,炎症反应,神经递质信号传导和大脑发育有关的基因。这些结果提供了对TBI恢复的复杂生物学的见解。

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