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Intestinal Surgery Contributes to Acute Cerebellar Ataxia Through Gut Brain Axis
Introduction: Acute cerebellar ataxia (ACA) is the most common form of pediatric ataxia. Changes in gut flora can modulate the nervous system, influencing brain function via the gut-brain axis (GBA). This study aimed to illustrate the relationship between intestinal microbiota and ACA. Method: A tot...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764330/ https://www.ncbi.nlm.nih.gov/pubmed/31616359 http://dx.doi.org/10.3389/fneur.2019.00995 |
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author | Yu, Jie Fan, Yuanming Wang, Li Huang, Yanjuan Xia, Jingyi Ding, Le Wu, Chun-Feng Lu, Xiaopeng Ma, Gaoxiang Kim, Samuel Zheng, Guo Guo, Hu Zhang, Gang |
author_facet | Yu, Jie Fan, Yuanming Wang, Li Huang, Yanjuan Xia, Jingyi Ding, Le Wu, Chun-Feng Lu, Xiaopeng Ma, Gaoxiang Kim, Samuel Zheng, Guo Guo, Hu Zhang, Gang |
author_sort | Yu, Jie |
collection | PubMed |
description | Introduction: Acute cerebellar ataxia (ACA) is the most common form of pediatric ataxia. Changes in gut flora can modulate the nervous system, influencing brain function via the gut-brain axis (GBA). This study aimed to illustrate the relationship between intestinal microbiota and ACA. Method: A total of 30 and 12 children were randomly sampled from history of intestinal surgery (HOIS) and no intestinal surgery groups (NHOIS), respectively. In addition, 10 healthy children who sought physical examination in Children's Hospital of Nanjing Medical University were recruited as a control group. The stool samples were 16S rRNA detected. Results: We observed that many ACA children had intestinal surgery history prior to the onset of ACA. The 16S rRNA sequencing indicated that HOIS and control groups were well-distinguished by principal component analysis. The discrepancy between HOIS and NHOIS groups were also displayed by principal component analysis score plot. However, no differences were found between NHOIS and control groups. The results of student's t-test were consistent with principal component analysis. A total of nine different genera were identified between HOIS and control groups. Five genera and a phylum showed significant differences between HOIS and NHOIS groups. Conclusion: Altered genera and phyla associated with ACA were identified. Our findings provide new insight into treating and preventing ACA. |
format | Online Article Text |
id | pubmed-6764330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67643302019-10-15 Intestinal Surgery Contributes to Acute Cerebellar Ataxia Through Gut Brain Axis Yu, Jie Fan, Yuanming Wang, Li Huang, Yanjuan Xia, Jingyi Ding, Le Wu, Chun-Feng Lu, Xiaopeng Ma, Gaoxiang Kim, Samuel Zheng, Guo Guo, Hu Zhang, Gang Front Neurol Neurology Introduction: Acute cerebellar ataxia (ACA) is the most common form of pediatric ataxia. Changes in gut flora can modulate the nervous system, influencing brain function via the gut-brain axis (GBA). This study aimed to illustrate the relationship between intestinal microbiota and ACA. Method: A total of 30 and 12 children were randomly sampled from history of intestinal surgery (HOIS) and no intestinal surgery groups (NHOIS), respectively. In addition, 10 healthy children who sought physical examination in Children's Hospital of Nanjing Medical University were recruited as a control group. The stool samples were 16S rRNA detected. Results: We observed that many ACA children had intestinal surgery history prior to the onset of ACA. The 16S rRNA sequencing indicated that HOIS and control groups were well-distinguished by principal component analysis. The discrepancy between HOIS and NHOIS groups were also displayed by principal component analysis score plot. However, no differences were found between NHOIS and control groups. The results of student's t-test were consistent with principal component analysis. A total of nine different genera were identified between HOIS and control groups. Five genera and a phylum showed significant differences between HOIS and NHOIS groups. Conclusion: Altered genera and phyla associated with ACA were identified. Our findings provide new insight into treating and preventing ACA. Frontiers Media S.A. 2019-09-20 /pmc/articles/PMC6764330/ /pubmed/31616359 http://dx.doi.org/10.3389/fneur.2019.00995 Text en Copyright © 2019 Yu, Fan, Wang, Huang, Xia, Ding, Wu, Lu, Ma, Kim, Zheng, Guo and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Yu, Jie Fan, Yuanming Wang, Li Huang, Yanjuan Xia, Jingyi Ding, Le Wu, Chun-Feng Lu, Xiaopeng Ma, Gaoxiang Kim, Samuel Zheng, Guo Guo, Hu Zhang, Gang Intestinal Surgery Contributes to Acute Cerebellar Ataxia Through Gut Brain Axis |
title | Intestinal Surgery Contributes to Acute Cerebellar Ataxia Through Gut Brain Axis |
title_full | Intestinal Surgery Contributes to Acute Cerebellar Ataxia Through Gut Brain Axis |
title_fullStr | Intestinal Surgery Contributes to Acute Cerebellar Ataxia Through Gut Brain Axis |
title_full_unstemmed | Intestinal Surgery Contributes to Acute Cerebellar Ataxia Through Gut Brain Axis |
title_short | Intestinal Surgery Contributes to Acute Cerebellar Ataxia Through Gut Brain Axis |
title_sort | intestinal surgery contributes to acute cerebellar ataxia through gut brain axis |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764330/ https://www.ncbi.nlm.nih.gov/pubmed/31616359 http://dx.doi.org/10.3389/fneur.2019.00995 |
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