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Potential Biomarkers for Diagnosis and Screening of Autism Spectrum Disorders

机译:潜在的生物标志物,用于诊断和筛查自闭症谱系障碍

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摘要

BACKGROUND: Autism spectrum disorder (ASD) is a highly heritable neurodevelopmental condition, which is typically characterized by a triad of symptoms: impaired social communication, social reciprocity and repetitive stereotypic behavior. While the behavioral phenotype of ASD is well described, the search for reliable ‘autism biomarkers’ continues. CONTENT: Insulin growth factor (IGF) is essential for the myelination of developing fetal neurons; this is in addition to the well-known links between IGF, maternal inflammation, infection and autism supporting IGF as a potential marker. Combining IGF data with data regarding levels of the known markers, serotonin and anti-myelin basic protein, in order to calculate an autism index, could provide a new diagnostic method for at-risk neonates. Disruptions to multiple pathophysiological systems, including redox, folate, methylation, tryptophan metabolism, and mitochondrial metabolism, have been well documented in autistic patients. Maternal infection and inflammation have known links with autism. Autoimmunity has therefore been a well-studied area of autism research. The potential of using autoantibodies as novel biomarkers for autism, in addition to providing insights into the neurodevelopmental processes that lead to autism. SUMMARY: The six proposed causes of autism involve both metabolic and immunologic dysfunctions and include: increased oxidative stress; decreased methionine metabolism and trans-sulfuration: aberrant free and bound metal burden; gastrointestinal (GI) disturbances; immune/inflammation dysregulation; and autoimmune targeting. A newborn screening program for early-onset ASD should be capable of utilizing a combination of ASD-associated biomarkers representative of the six proposed causes of autism in order to identify newborns at risk. The biomarkers discussed in this article are useful to guide the selection, efficacy and sufficiency of biomedical interventions, which would likely include nutritional supplementation, dietary changes and specific medications for treating GI pathogens and reducing inflammation. KEYWORDS: ASD, autism, biomarkers, newborn screening, diagnosis.
机译:背景:自闭症谱系障碍(ASD)是一种高度遗传的神经发育病症,其通常是三合一症状的特征:社会沟通受损,社会互惠和重复的陈规定型行为。虽然ASD的行为表型很好地描述,但寻求可靠的“自闭症生物标志物”的继续。含量:胰岛素生长因子(IGF)对于开发胎儿神经元的髓鞘产生至关重要;除了IGF,母体炎症,感染和自闭症之间的众所周知的链接,支持IGF作为潜在标记。将IGF数据与关于已知标志物,血清素和抗髓鞘碱性蛋白水平的数据组合,以便计算自闭症指数,可以为风险新生儿提供新的诊断方法。在自闭症患者中,对多种病理生理体系的破坏,包括氧化还原,叶酸,甲基化,色氨酸代谢和线粒体代谢。母体感染和炎症与自闭症有关。因此,自身免疫已经是一个研究的自闭症研究领域。除了向导致自闭症的神经发育过程中的见解外,使用自身抗体作为自闭症的新生物标志物的潜力。摘要:六种拟议的自闭症原因涉及代谢和免疫功能性功能障碍,包括:增加氧化应激;降低甲硫氨酸代谢和反式硫化:异常自由和结合的金属负荷;胃肠道(GI)干扰;免疫/炎症失呼;和自身免疫目标。用于早期发病ASD的新生儿筛查计划应该能够利用代表六个拟议的自闭症原因的ASD相关生物标志物组合,以识别风险的新生儿。本文讨论的生物标志物可用于指导生物医学干预的选择,疗效和充分性,这可能包括用于治疗GI病原体和减少炎症的营养补充剂,饮食变化和特定药物。关键词:ASD,自闭症,生物标志物,新生儿筛查,诊断。

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  • 作者

    Anna Meiliana; Andi Wijaya;

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  • 年度 2014
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  • 正文语种 eng
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