首页> 外文期刊>Brain Sciences >Genome, Environment, Microbiome and Metabolome in Autism (GEMMA) Study Design: Biomarkers Identification for Precision Treatment and Primary Prevention of Autism Spectrum Disorders by an Integrated Multi-Omics Systems Biology Approach
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Genome, Environment, Microbiome and Metabolome in Autism (GEMMA) Study Design: Biomarkers Identification for Precision Treatment and Primary Prevention of Autism Spectrum Disorders by an Integrated Multi-Omics Systems Biology Approach

机译:基因组,环境,微生物组和代谢物中的自闭症(Gemma)研究设计:Biomarkers通过集成多OMICS系统生物学方法识别精确治疗和初步预防自闭症谱系统障碍

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Autism Spectrum Disorder (ASD) affects approximately 1 child in 54, with a 35-fold increase since 1960. Selected studies suggest that part of the recent increase in prevalence is likely attributable to an improved awareness and recognition, and changes in clinical practice or service availability. However, this is not sufficient to explain this epidemiological phenomenon. Research points to a possible link between ASD and intestinal microbiota because many children with ASD display gastro-intestinal problems. Current large-scale datasets of ASD are limited in their ability to provide mechanistic insight into ASD because they are predominantly cross-sectional studies that do not allow evaluation of perspective associations between early life microbiota composition/function and later ASD diagnoses. Here we describe GEMMA (Genome, Environment, Microbiome and Metabolome in Autism), a prospective study supported by the European Commission, that follows at-risk infants from birth to identify potential biomarker predictors of ASD development followed by validation on large multi-omics datasets. The project includes clinical (observational and interventional trials) and pre-clinical studies in humanized murine models (fecal transfer from ASD probands) and in vitro colon models. This will support the progress of a microbiome-wide association study (of human participants) to identify prognostic microbiome signatures and metabolic pathways underlying mechanisms for ASD progression and severity and potential treatment response.
机译:自闭症谱系障碍(ASD)影响了54名儿童,自1960年以来增加了35倍。所选研究表明,最近普遍增加的部分可能会归因于改善的认识和认可,以及临床实践或服务的变化可用性。然而,这不足以解释这种流行病学现象。研究指出ASD和肠道微生物群之间可能的联系,因为许多具有ASD展示胃肠问题的儿童。 ASD的当前大规模数据集是有限的,他们能够提供对ASD的机械洞察力的能力,因为它们主要是横截面研究,其不允许评估早期生命微生物群组合/功能和后面的ASD诊断之间的透视关联。在这里,我们描述了欧洲委员会支持的杰玛(基因组,环境,微生物和代谢物),欧洲委员会支持的前瞻性研究,涉及出生的风险婴儿,以确定ASD开发的潜在生物标志物预测因子,然后对大型多OMICS数据集进行验证。该项目包括临床(观察和介入试验)和人源鼠模型的临床研究(来自ASD证据的粪便转移)和体外结肠模型。这将支持微生物组 - 宽协会研究(人参与者)的进展,以鉴定亚本症进展和严重程度和潜在治疗反应的预后微生物组签名和代谢途径。

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