4.6 Article

The Gut Microbiota and Associated Metabolites Are Altered in Sleep Disorder of Children With Autism Spectrum Disorders

Journal

FRONTIERS IN PSYCHIATRY
Volume 11, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fpsyt.2020.00855

Keywords

gut microbiota; metabolism; autism spectrum disorders; sleep disorder; microbiota-gut-brain axis

Categories

Funding

  1. Key Scientific and Technological Projects of Guangdong Province [2018B030335001]
  2. Guangzhou City [202007030002]

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Background Autism spectrum disorder (ASD) is a type of neurodevelopmental disease that is frequently accompanied by sleep disorder. Herein, we investigated changes in the gut microbiota and its metabolites correlated with core symptoms and sleep problems in children with ASD. Methods One hundred and twenty children diagnosed with ASD based on Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria were enrolled in our study. The Autism Behavior Checklist (ABC), Social Responsiveness Scale (SRS), and Childhood Autism Rating Scale (CARS) were used to assess autism symptoms, and the Children Sleep Habits Questionnaire (CSHQ) was employed to evaluate sleep problems in children with ASD. The 120 children were divided into a sleep disorder group (n = 60) and a control group without sleep disorder (n = 60) according to the CSHQ answers. Illumina MiSeq analysis of 16S rRNA genes was used to compare differences in gut microbiota, and metabolomics analysis was employed to asses associated metabolites. Results SRS and CARS scores for the sleep disorder group were significantly higher than for the control group (p< 0.05). The abundances of butyrate-producing bacteriaFaecalibacteriumandAgathobacterwere reduced significantly in the sleep disorder group (p< 0.05), and this was negatively correlated with CSHQ score (p= 0.007 andp= 0.014, respectively). The abundance ofAgathobacterwas also negatively associated with the ABC language score (p= 0.044). Furthermore, levels of 3-hydroxybutyric acid and melatonin were significantly lower (p< 0.05) while serotonin levels were higher (p< 0.05) in the sleep disorder group. The 3-hydroxybutyric acid level was positively associated withFaecalibacteriumabundance (p= 0.000), and melatonin was positively associated with the abundance ofFaecalibacterium(p= 0.036) andAgathobacter(p= 0.041). We also observed negative correlations between 3-hydroxybutyric acid and CSHQ (p= 0.000) and CARS (p= 0.009), between melatonin and CSHQ (p= 0.002) and ABC sensory score (p= 0.021), and a positive correlation between serotonin and CSHQ (p= 0.002) and ABC sensory score (p= 0.025). Conclusions ASD children with sleep disorder exhibited declines in the abundance ofFaecalibacteriumandAgathobacter, decreased levels of 3-hydroxybutyric acid and melatonin, and an increase in serotonin. These changes may aggravate sleep problems and core symptoms in children with ASD.

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