Department of Preventive Medicine and Public Health, Universidad de Zaragoza, Zaragoza, Spain.
Department of Biochemistry and Molecular and Cell Biology, Universidad de Zaragoza, Zaragoza, Spain; Instituto Agroalimentario de Aragón - IA2- (Universidad de Zaragoza - CITA), Zaragoza, Spain; Instituto de Investigación Sanitaria de Aragón (IIS Aragón), Zaragoza, Spain.
Asian J Psychiatr. 2020 Jan;47:101874. doi: 10.1016/j.ajp.2019.101874. Epub 2019 Nov 12.
The high frequency of functional gastrointestinal disorders (FGIDs) in autism spectrum disorders (ASD) has drawn attention to the composition of gut microbiota as a possible factor in ASD pathogenesis. However, characterization of a distinctive ASD microbial pattern is still unclear.
To conduct a narrative review on ASD microbial profile and diversity changes relative to NT children and FGID comorbidity and ASD pathogenesis.
First, we searched the PubMed database in peer-reviewed journals for evidence regarding the current epidemiological evidence on FGID comorbidity. For the identification of a microbial profile in ASD children, only original studies examining gut bacterial and fungal abundances and diversity in ASD children and adolescents were included. Lastly, research on the role of microbial dysbiosis as an interface between genetic and environmental risk factors in the pathogenesis of neuropsychiatric disorders, and specifically ASD, was examined.
Prevalence and risk of FGIDs is significantly higher in ASD children and correlates with the severity of ASD. Bacterial and fungal diversity differ between ASD and NT children, indicating a difference in taxonomic abundance profiles, which have been reported at all bacterial phylogenetic levels. However, studies analyzing gut microbiota have a heterogeneous methodology and several limitations that could account for the variety of findings for each taxon. Also, covariate analysis reveals influence of demographics, diet, disease severity, GI comorbidity and allergies. Integration of these findings with changes in metabolome and genetic risk factors allowed for a better understanding of microbiota involvement in ASD pathogenesis for future research.
自闭症谱系障碍(ASD)中功能性胃肠疾病(FGIDs)的高发率引起了人们对肠道微生物群落组成作为 ASD 发病机制中一个可能因素的关注。然而,具有独特 ASD 微生物模式的特征仍然不清楚。
对 ASD 微生物特征和多样性变化进行叙述性综述,这些变化与 NT 儿童和 FGID 共病以及 ASD 发病机制有关。
首先,我们在同行评审期刊的 PubMed 数据库中搜索了有关 FGID 共病的当前流行病学证据。为了确定 ASD 儿童的微生物特征,仅纳入了检查 ASD 儿童肠道细菌和真菌丰度和多样性的原始研究。最后,研究了微生物失调作为遗传和环境风险因素在神经精神疾病发病机制中(特别是 ASD)的接口作用。
FGIDs 的患病率和风险在 ASD 儿童中显著更高,并且与 ASD 的严重程度相关。ASD 儿童和 NT 儿童之间的细菌和真菌多样性存在差异,表明分类丰度图谱存在差异,这在所有细菌系统发育水平上都有报道。然而,分析肠道微生物组的研究具有异质的方法和多种局限性,这些局限性可能解释了每个分类群的各种发现。此外,协变量分析揭示了人口统计学、饮食、疾病严重程度、GI 共病和过敏的影响。将这些发现与代谢组和遗传风险因素的变化相结合,有助于更好地理解微生物在 ASD 发病机制中的作用,为未来的研究提供了依据。