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Postmortem Studies of Neuroinflammation in Autism Spectrum Disorder: a Systematic Review

机译:自闭症谱系疾病中神经炎症的后期研究:系统评价

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Although the neurobiological basis for autism spectrum disorder (ASD) has not yet been fully clarified, converging lines of evidence implicated a role of neuroinflammation in the etiological pathway of this disorder. The present article provided a systematic review of publications regarding the involvement of different components of neuroinflammation in postmortem brain samples of subjects diagnosed with ASD. A systematic search of PubMed, Embase, and Web of Science was conducted, which was supplemented by manual searching of reference lists of included articles. The screening for study and extraction of data were conducted by two independent authors after reviewing the abstract and full text. Of 356 articles identified in the literature search, 27 articles comprising 685 subjects (ASD = 313, controls = 351, schizophrenia = 10, epilepsy = 11) covering 19 brain regions met the eligibility criteria for this review. The search yielded 11 studies that estimated astrocyte-related changes, 8 studies that reported microglia-related changes, 2 studies that evaluated oligodendrocyte-related changes, 3 studies that examined changes in glial cells without differentiating cell types, 6 studies that evaluated the levels of cytokines and chemokines, and 7 studies that measured other inflammatory parameters in postmortem brain samples of subjects with ASD compared with controls. Although a few studies noted a lack of changes in neuroinflammatory markers in postmortem brain samples of ASD subjects, the majority of studies supported the presence of neuroinflammation in the neurobiological pattern of ASD as shown by activation of astrocytes and microglia together with abnormal levels of cytokines and chemokines.
机译:虽然自闭症谱系障碍(ASD)的神经生物学基础尚未完全澄清,但融合了证据线条对该疾病的病因途径致力于神经炎症的作用。本文提供了对有关诊断疗效的受试者的后期脑样品中神经炎性炎症的不同组分的出版物的系统审查。进行了对Pubmed,Embase和Science Web进行了系统的系统搜索,通过手动搜索包含的文章的参考列表补充。在审查抽象和全文后,两个独立的作者进行了研究和提取数据的筛选。在文献搜索中确定的356篇文章,27种包含685-6-6个受试者(ASD = 313,对照= 351,Schizopheria = 10,癫痫= 11)覆盖19脑区域的审查资格标准。该搜索的11项研究估计了星形胶质细胞相关的变化,8项研究报告了与微胶质相关变化的研究,2研究评估了少突胶质细胞相关变化的研究,3研究,在不区分细胞类型的情况下检查胶质细胞的变化,6项研究评估了细胞因子和趋化因子,以及7项研究,以与对照组的受试者的后期脑样品中测量其他炎症参数。虽然一些研究指出的是ASD受试者的后期脑样本中神经胰腺炎患者的缺乏变化,但大多数研究都支持在ASD的神经生理学模式中存在神经炎性的存在,如半胶质细胞和微胶质的激活和细胞因子的异常水平所示。趋化因子。

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