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Ketogenic diet poses a significant effect on imbalanced gut microbiota in infants with refractory epilepsy
AIM: To investigate whether patients with refractory epilepsy and healthy infants differ in gut microbiota (GM), and how ketogenic diet (KD) alters GM. METHODS: A total of 14 epileptic and 30 healthy infants were recruited and seizure frequencies were recorded. Stool samples were collected for 16S r...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597508/ https://www.ncbi.nlm.nih.gov/pubmed/28970732 http://dx.doi.org/10.3748/wjg.v23.i33.6164 |
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author | Xie, Gan Zhou, Qian Qiu, Chuang-Zhao Dai, Wen-Kui Wang, He-Ping Li, Yin-Hu Liao, Jian-Xiang Lu, Xin-Guo Lin, Su-Fang Ye, Jing-Hua Ma, Zhuo-Ya Wang, Wen-Jian |
author_facet | Xie, Gan Zhou, Qian Qiu, Chuang-Zhao Dai, Wen-Kui Wang, He-Ping Li, Yin-Hu Liao, Jian-Xiang Lu, Xin-Guo Lin, Su-Fang Ye, Jing-Hua Ma, Zhuo-Ya Wang, Wen-Jian |
author_sort | Xie, Gan |
collection | PubMed |
description | AIM: To investigate whether patients with refractory epilepsy and healthy infants differ in gut microbiota (GM), and how ketogenic diet (KD) alters GM. METHODS: A total of 14 epileptic and 30 healthy infants were recruited and seizure frequencies were recorded. Stool samples were collected for 16S rDNA sequencing using the Illumina Miseq platform. The composition of GM in each sample was analyzed with MOTHUR, and inter-group comparison was conducted by R software. RESULTS: After being on KD treatment for a week, 64% of epileptic infants showed an obvious improvement, with a 50% decrease in seizure frequency. GM structure in epileptic infants (P1 group) differed dramatically from that in healthy infants (Health group). Proteobacteria, which had accumulated significantly in the P1 group, decreased dramatically after KD treatment (P2 group). Cronobacter predominated in the P1 group and remained at a low level both in the Health and P2 groups. Bacteroides increased significantly in the P2 group, in which Prevotella and Bifidobacterium also grew in numbers and kept increasing. CONCLUSION: GM pattern in healthy infants differed dramatically from that of the epileptic group. KD could significantly modify symptoms of epilepsy and reshape the GM of epileptic infants. |
format | Online Article Text |
id | pubmed-5597508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-55975082017-10-02 Ketogenic diet poses a significant effect on imbalanced gut microbiota in infants with refractory epilepsy Xie, Gan Zhou, Qian Qiu, Chuang-Zhao Dai, Wen-Kui Wang, He-Ping Li, Yin-Hu Liao, Jian-Xiang Lu, Xin-Guo Lin, Su-Fang Ye, Jing-Hua Ma, Zhuo-Ya Wang, Wen-Jian World J Gastroenterol Retrospective Study AIM: To investigate whether patients with refractory epilepsy and healthy infants differ in gut microbiota (GM), and how ketogenic diet (KD) alters GM. METHODS: A total of 14 epileptic and 30 healthy infants were recruited and seizure frequencies were recorded. Stool samples were collected for 16S rDNA sequencing using the Illumina Miseq platform. The composition of GM in each sample was analyzed with MOTHUR, and inter-group comparison was conducted by R software. RESULTS: After being on KD treatment for a week, 64% of epileptic infants showed an obvious improvement, with a 50% decrease in seizure frequency. GM structure in epileptic infants (P1 group) differed dramatically from that in healthy infants (Health group). Proteobacteria, which had accumulated significantly in the P1 group, decreased dramatically after KD treatment (P2 group). Cronobacter predominated in the P1 group and remained at a low level both in the Health and P2 groups. Bacteroides increased significantly in the P2 group, in which Prevotella and Bifidobacterium also grew in numbers and kept increasing. CONCLUSION: GM pattern in healthy infants differed dramatically from that of the epileptic group. KD could significantly modify symptoms of epilepsy and reshape the GM of epileptic infants. Baishideng Publishing Group Inc 2017-09-07 2017-09-07 /pmc/articles/PMC5597508/ /pubmed/28970732 http://dx.doi.org/10.3748/wjg.v23.i33.6164 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Retrospective Study Xie, Gan Zhou, Qian Qiu, Chuang-Zhao Dai, Wen-Kui Wang, He-Ping Li, Yin-Hu Liao, Jian-Xiang Lu, Xin-Guo Lin, Su-Fang Ye, Jing-Hua Ma, Zhuo-Ya Wang, Wen-Jian Ketogenic diet poses a significant effect on imbalanced gut microbiota in infants with refractory epilepsy |
title | Ketogenic diet poses a significant effect on imbalanced gut microbiota in infants with refractory epilepsy |
title_full | Ketogenic diet poses a significant effect on imbalanced gut microbiota in infants with refractory epilepsy |
title_fullStr | Ketogenic diet poses a significant effect on imbalanced gut microbiota in infants with refractory epilepsy |
title_full_unstemmed | Ketogenic diet poses a significant effect on imbalanced gut microbiota in infants with refractory epilepsy |
title_short | Ketogenic diet poses a significant effect on imbalanced gut microbiota in infants with refractory epilepsy |
title_sort | ketogenic diet poses a significant effect on imbalanced gut microbiota in infants with refractory epilepsy |
topic | Retrospective Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597508/ https://www.ncbi.nlm.nih.gov/pubmed/28970732 http://dx.doi.org/10.3748/wjg.v23.i33.6164 |
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