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Deviated and early unsustainable stunted development of gut microbiota in children with autism spectrum disorder.
Lou, Mingxing; Cao, Aihua; Jin, Cuiyuan; Mi, Kai; Xiong, Xiyue; Zeng, Zhaoyang; Pan, Xu; Qie, Jinlong; Qiu, Shangfeng; Niu, Yaofang; Liang, Hao; Liu, Yanping; Chen, Lin; Liu, Zhi; Zhao, Qing; Qiu, Xiyan; Jin, Yuanxiang; Sheng, Xiaoqi; Hu, Zhibin; Jin, Gulei; Liu, Jingshi; Liu, Xingyin; Wang, Yichao.
Afiliação
  • Lou M; National Health Commission (NHC) Key Laboratory of Birth Defect for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, China.
  • Cao A; Department of Pediatrics, Shandong University Qilu Hospital, Jinan, Shandong, China.
  • Jin C; Institute of Translational Medicine, Zhejiang Shuren University, Hangzhou, Zhejiang, China.
  • Mi K; State Key Laboratory of Reproductive Medicine, Key Laboratory of Pathogen of Jiangsu Province, Key Laboratory of Human Functional Genomics of Jiangsu Province Center of Global Health, Nanjing Medical University, Nanjing, Jiangsu, China.
  • Xiong X; National Health Commission (NHC) Key Laboratory of Birth Defect for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, China.
  • Zeng Z; Institute of Translational Medicine, Zhejiang Shuren University, Hangzhou, Zhejiang, China.
  • Pan X; College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
  • Qie J; State Key Laboratory of Reproductive Medicine, Key Laboratory of Pathogen of Jiangsu Province, Key Laboratory of Human Functional Genomics of Jiangsu Province Center of Global Health, Nanjing Medical University, Nanjing, Jiangsu, China.
  • Qiu S; National Health Commission (NHC) Key Laboratory of Birth Defect for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, China.
  • Niu Y; Guhe Information Technology Co Ltd, Hangzhou, China.
  • Liang H; National Health Commission (NHC) Key Laboratory of Birth Defect for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, China.
  • Liu Y; National Health Commission (NHC) Key Laboratory of Birth Defect for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, China.
  • Chen L; National Health Commission (NHC) Key Laboratory of Birth Defect for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, China.
  • Liu Z; State Key Laboratory of Reproductive Medicine, Key Laboratory of Pathogen of Jiangsu Province, Key Laboratory of Human Functional Genomics of Jiangsu Province Center of Global Health, Nanjing Medical University, Nanjing, Jiangsu, China.
  • Zhao Q; State Key Laboratory of Reproductive Medicine, Key Laboratory of Pathogen of Jiangsu Province, Key Laboratory of Human Functional Genomics of Jiangsu Province Center of Global Health, Nanjing Medical University, Nanjing, Jiangsu, China.
  • Qiu X; National Health Commission (NHC) Key Laboratory of Birth Defect for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, China.
  • Jin Y; College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou, Zhejiang, China.
  • Sheng X; National Health Commission (NHC) Key Laboratory of Birth Defect for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, China.
  • Hu Z; State Key Laboratory of Reproductive Medicine, Center of Global Health, Nanjing Medical University, Nanjing, Jiangsu, China.
  • Jin G; Guhe Information Technology Co Ltd, Hangzhou, China xingyinliu@njmu.edu.cn guleijin@126.com ylisaoydwxy@126.com lisaoydwxy@yeah.net.
  • Liu J; National Health Commission (NHC) Key Laboratory of Birth Defect for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, China xingyinliu@njmu.edu.cn guleijin@126.com ylisaoydwxy@126.com lisaoydwxy@yeah.net.
  • Liu X; State Key Laboratory of Reproductive Medicine, Key Laboratory of Pathogen of Jiangsu Province, Key Laboratory of Human Functional Genomics of Jiangsu Province Center of Global Health, Nanjing Medical University, Nanjing, Jiangsu, China xingyinliu@njmu.edu.cn guleijin@126.com ylisaoydwxy@126.com lisa
  • Wang Y; National Health Commission (NHC) Key Laboratory of Birth Defect for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, China xingyinliu@njmu.edu.cn guleijin@126.com ylisaoydwxy@126.com lisaoydwxy@yeah.net.
Gut ; 71(8): 1588-1599, 2022 08.
Article em En | MEDLINE | ID: mdl-34930815
ABSTRACT

OBJECTIVE:

Recent studies have provided insights into the gut microbiota in autism spectrum disorder (ASD); however, these studies were restricted owing to limited sampling at the unitary stage of childhood. Herein, we aimed to reveal developmental characteristics of gut microbiota in a large cohort of subjects with ASD combined with interindividual factors impacting gut microbiota.

DESIGN:

A large cohort of 773 subjects with ASD (aged 16 months to 19 years), 429 neurotypical (NT) development subjects (aged 11 months to 15 years) were emolyed to determine the dynamics change of gut microbiota across different ages using 16S rRNA sequencing.

RESULT:

In subjects with ASD, we observed a distinct but progressive deviation in the development of gut microbiota characterised by persistently decreased alpha diversity, early unsustainable immature microbiota, altered aboudance of 20 operational taxonomic units (OTUs), decreased taxon detection rate and 325 deregulated microbial metabolic functions with age-dependent patterns. We further revealed microbial relationships that have changed extensively in ASD before 3 years of age, which were associated with the severity of behaviour, sleep and GI symptoms in the ASD group. This analysis demonstrated that a signature of the combination of 2 OTUs, Veillonella and Enterobacteriaceae, and 17 microbial metabolic functions efficiently discriminated ASD from NT subjects in both the discovery (area under the curve (AUC)=0.86), and validation 1 (AUC=0.78), 2 (AUC=0.82) and 3 (AUC=0.67) sets.

CONCLUSION:

Our large cohort combined with clinical symptom analysis highlights the key regulator of gut microbiota in the pathogenesis of ASD and emphasises the importance of monitoring and targeting the gut microbiome in future clinical applications of ASD.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Microbiota / Transtorno do Espectro Autista / Microbioma Gastrointestinal Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Revista: Gut Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Microbiota / Transtorno do Espectro Autista / Microbioma Gastrointestinal Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Revista: Gut Ano de publicação: 2022 Tipo de documento: Article