Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, 149 13th Street Charlestown, Boston, MA 02129, USA.
Harvard Medical School, Boston, 25 Shattuck Street, Boston, MA 02115, USA.
Nutrients. 2019 Sep 6;11(9):2128. doi: 10.3390/nu11092128.
Autism Spectrum Disorder (ASD) is a complex neurological and developmental disorder characterized by behavioral and social impairments as well as multiple co-occurring conditions, such as gastrointestinal abnormalities, dental/periodontal diseases, and allergies. The etiology of ASD likely involves interaction between genetic and environmental factors. Recent studies suggest that oral and gut microbiome play important roles in the pathogenesis of inflammation, immune dysfunction, and disruption of the gut-brain axis, which may contribute to ASD pathophysiology. The majority of previous studies used unrelated neurotypical individuals as controls, and they focused on the gut microbiome, with little attention paid to the oral flora. In this pilot study, we used a first degree-relative matched design combined with high fidelity 16S rRNA (ribosomal RNA) gene amplicon sequencing in order to characterize the oral and gut microbiotas of patients with ASD compared to neurotypical individuals, and explored the utility of microbiome markers for ASD diagnosis and subtyping of clinical comorbid conditions. Additionally, we aimed to develop microbiome biomarkers to monitor responses to a subsequent clinical trial using probiotics supplementation. We identified distinct features of gut and salivary microbiota that differed between ASD patients and neurotypical controls. We next explored the utility of some differentially enriched markers for ASD diagnosis and examined the association between the oral and gut microbiomes using network analysis. Due to the tremendous clinical heterogeneity of the ASD population, we explored the relationship between microbiome and clinical indices as an attempt to extract microbiome signatures assocociated with clinical subtypes, including allergies, abdominal pain, and abnormal dietary habits. The diagnosis of ASD currently relies on psychological testing with potentially high subjectivity. Given the emerging role that the oral and gut microbiome plays in systemic diseases, our study will provide preliminary evidence for developing microbial markers that can be used to diagnose or guide treatment of ASD and comorbid conditions. These preliminary results also serve as a starting point to test whether altering the oral and gut microbiome could improve co-morbid conditions in patients with ASD and further modify the core symptoms of ASD.
自闭症谱系障碍(ASD)是一种复杂的神经发育障碍,其特征为行为和社交障碍,以及多种并发疾病,如胃肠道异常、口腔/牙周疾病和过敏等。ASD 的病因可能涉及遗传和环境因素的相互作用。最近的研究表明,口腔和肠道微生物群在炎症、免疫功能障碍和肠道-大脑轴紊乱的发病机制中发挥着重要作用,这可能有助于 ASD 的病理生理学。以前的大多数研究都使用不相关的神经典型个体作为对照,并且主要关注肠道微生物群,而对口腔菌群的关注较少。在这项初步研究中,我们使用一级亲属匹配设计结合高保真 16S rRNA(核糖体 RNA)基因扩增子测序,以比较 ASD 患者与神经典型个体的口腔和肠道微生物组,并探索微生物组标志物在 ASD 诊断和临床共病亚型中的应用。此外,我们旨在开发微生物组生物标志物,以监测随后使用益生菌补充剂的临床试验的反应。我们确定了 ASD 患者和神经典型对照组之间肠道和唾液微生物组不同的特征。我们接下来探索了一些差异富集的标记物在 ASD 诊断中的应用,并使用网络分析检查了口腔和肠道微生物组之间的关联。由于 ASD 人群的临床异质性很大,我们探索了微生物组与临床指标之间的关系,试图提取与临床亚型相关的微生物组特征,包括过敏、腹痛和异常饮食习惯。ASD 的诊断目前依赖于具有潜在高度主观性的心理测试。鉴于口腔和肠道微生物组在系统性疾病中的作用日益显现,我们的研究将为开发可用于诊断或指导 ASD 及共病治疗的微生物标志物提供初步证据。这些初步结果也为测试改变口腔和肠道微生物组是否可以改善 ASD 患者的共病状况以及进一步改变 ASD 的核心症状提供了一个起点。