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Potential Biomarkers for Diagnosis and Screening of Autism Spectrum Disorders

机译:诊断和筛选自闭症谱系障碍的潜在生物标志物

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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\u27 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.
机译:背景:自闭症谱系障碍(ASD)是一种高度可遗传的神经发育疾病,通常表现为三联征:社交沟通受损,社交互惠和重复刻板行为。虽然对ASD的行为表型进行了很好的描述,但仍在寻找可靠的“自闭症生物标志物”。内容:胰岛素生长因子(IGF)对于发育中的胎儿神经元的髓鞘形成至关重要;这是IGF,孕产妇炎症,感染和自闭症之间众所周知的联系的补充,支持IGF作为潜在标志物。将IGF数据与有关已知标志物,5-羟色胺和抗髓鞘碱性蛋白水平的数据相结合,以计算自闭症指数,可以为高危新生儿提供一种新的诊断方法。自闭症患者已被证明对多种病理生理系统的破坏,包括氧化还原,叶酸,甲基化,色氨酸代谢和线粒体代谢。产妇感染和炎症与自闭症有已知的联系。因此,自身免疫一直是自闭症研究的一个被充分研究的领域。总结:自闭症的六个提出原因涉及代谢和免疫功能障碍,包括:氧化应激增加;自闭症的六种原因。蛋氨酸代谢和反式硫减少:游离和结合的金属负荷异常;胃肠道(GI)障碍;免疫/炎症失调;和自身免疫靶向。早期筛查ASD的新生儿筛查程序应能够利用代表六个自闭症拟议病因的ASD相关生物标志物的组合,以识别有风险的新生儿。本文中讨论的生物标志物可用于指导生物医学干预措施的选择,功效和充分性,其中可能包括营养补充,饮食变化和用于治疗胃肠道病原体和减轻炎症的特定药物。

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