Altered Gut Microbiota and Short-chain Fatty Acids in Chinese Children with Constipated Autism Spectrum Disorder

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作者
Jianquan He
Xiuhua Gong
Bing Hu
Lin Lin
Xiujuan Lin
Wenxiu Gong
Bangzhou Zhang
Man Cao
Yanzhi Xu
Rongmu Xia
Guohua Zheng
Shuijin Wu
Yuying Zhang
机构
[1] Fujian University of Traditional Chinese Medicine,College of Rehabilitation Medicine
[2] Zhongshan Hospital of Xiamen University,Department of Rehabilitation, School of Medicine
[3] Xiamen University,School of Nursing
[4] Xiamen Institute of Big Data of TCM Constitution and PreventiveTreatment for Disease,Department of Pediatrics
[5] Qingdao University,School of Medicine
[6] Yichun People’s Hospital,Clinical Research Institute
[7] Xiamen University,College of Nursing and Health Management
[8] Xiamen Treatgut Biotechnology Co.,Department of Gastroenterology
[9] Ltd,undefined
[10] The Second Affiliated Hospital of Fujian University of Traditional Chinese Medicine,undefined
[11] Shanghai University of Medicine and Health Sciences,undefined
[12] Xiamen Food and Drug Evaluation and Adverse Reaction Monitoring Center,undefined
[13] Weifang People’s Hospital,undefined
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摘要
Gastrointestinal symptoms are more prevalent in children with autism spectrum disorder (ASD) than in typically developing (TD) children. Constipation is a significant gastrointestinal comorbidity of ASD, but the associations among constipated autism spectrum disorder (C-ASD), microbiota and short-chain fatty acids (SCFAs) are still debated. We enrolled 80 children, divided into the C-ASD group (n = 40) and the TD group (n = 40). In this study, an integrated 16S rRNA gene sequencing and gas chromatography–mass spectrometry-based metabolomics approach was applied to explore the association of the gut microbiota and SCFAs in C-ASD children in China. The community diversity estimated by the Observe, Chao1, and ACE indices was significantly lower in the C-ASD group than in the TD group. We observed that Ruminococcaceae_UCG_002, Erysipelotrichaceae_UCG_003, Phascolarctobacterium, Megamonas, Ruminiclostridium_5, Parabacteroides, Prevotella_2, Fusobacterium, and Prevotella_9 were enriched in the C-ASD group, and Anaerostipes, Lactobacillus, Ruminococcus_gnavus_group, Lachnospiraceae_NK4A136_group, Ralstonia, Eubacterium_eligens_group, and Ruminococcus_1 were enriched in the TD group. The propionate levels, which were higher in the C-ASD group, were negatively correlated with the abundance of Lactobacillus taxa, but were positively correlated with the severity of ASD symptoms. The random forest model, based on the 16 representative discriminant genera, achieved a high accuracy (AUC = 0.924). In conclusion, we found that C-ASD is related to altered gut microbiota and SCFAs, especially decreased abundance of Lactobacillus and excessive propionate in faeces, which provide new clues to understand C-ASD and biomarkers for the diagnosis and potential strategies for treatment of the disorder. This study was registered in the Chinese Clinical Trial Registry (www.chictr.org.cn; trial registration number ChiCTR2100052106; date of registration: October 17, 2021).
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