Cargando…
Altered fecal microbiota composition in individuals who abuse methamphetamine
As a severe public health problem, methamphetamine (METH) abuse places a heavy burden on families and society. A growing amount of evidence has indicated communication between gut microbiota and the CNS in drug addiction, with associations to neural, endocrine and immune pathways. Thus, we searched...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8437956/ https://www.ncbi.nlm.nih.gov/pubmed/34518605 http://dx.doi.org/10.1038/s41598-021-97548-1 |
_version_ | 1783752265256927232 |
---|---|
author | Yang, Yongde Yu, Xuan Liu, Xuebing Liu, Guangya Zeng, Kuan Wang, Gang |
author_facet | Yang, Yongde Yu, Xuan Liu, Xuebing Liu, Guangya Zeng, Kuan Wang, Gang |
author_sort | Yang, Yongde |
collection | PubMed |
description | As a severe public health problem, methamphetamine (METH) abuse places a heavy burden on families and society. A growing amount of evidence has indicated communication between gut microbiota and the CNS in drug addiction, with associations to neural, endocrine and immune pathways. Thus, we searched for alterations in the gut microbiota and their potential effects in METH users through 16S rRNA gene sequencing. A decreased Shannon index indicated lower bacterial diversity in the METH users than in the age-matched control group. The gut microbial community composition in the METH users was also altered, including reductions in Deltaproteobacteria and Bacteroidaceae abundances and increases in Sphingomonadales, Xanthomonadales, Romboutsia and Lachnospiraceae abundances. Moreover, the Fusobacteria abundance was correlated with the duration of METH use. Enterobacteriaceae, Ruminococcaceae, Bacteroides, and Faecalibacterium had statistically significant correlations with items related to the positive and negative symptoms of schizophrenia and to general psychopathology in the METH users, and all have previously been reported to be altered in individuals with psychotic syndromes, especially depression. Abstraction, one of the items of the cognitive assessment, was positively related to Blautia. These findings revealed alterations in the gut microbiota of METH users, and these alterations may play a role in psychotic syndrome and cognitive impairment. Although the mechanisms behind the links between these disorders and METH abuse are unknown, the relationships may indicate similarities in the pathogenesis of psychosis induced by METH abuse and other causes, providing a new paradigm for addiction and METH use disorder treatment. |
format | Online Article Text |
id | pubmed-8437956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84379562021-09-15 Altered fecal microbiota composition in individuals who abuse methamphetamine Yang, Yongde Yu, Xuan Liu, Xuebing Liu, Guangya Zeng, Kuan Wang, Gang Sci Rep Article As a severe public health problem, methamphetamine (METH) abuse places a heavy burden on families and society. A growing amount of evidence has indicated communication between gut microbiota and the CNS in drug addiction, with associations to neural, endocrine and immune pathways. Thus, we searched for alterations in the gut microbiota and their potential effects in METH users through 16S rRNA gene sequencing. A decreased Shannon index indicated lower bacterial diversity in the METH users than in the age-matched control group. The gut microbial community composition in the METH users was also altered, including reductions in Deltaproteobacteria and Bacteroidaceae abundances and increases in Sphingomonadales, Xanthomonadales, Romboutsia and Lachnospiraceae abundances. Moreover, the Fusobacteria abundance was correlated with the duration of METH use. Enterobacteriaceae, Ruminococcaceae, Bacteroides, and Faecalibacterium had statistically significant correlations with items related to the positive and negative symptoms of schizophrenia and to general psychopathology in the METH users, and all have previously been reported to be altered in individuals with psychotic syndromes, especially depression. Abstraction, one of the items of the cognitive assessment, was positively related to Blautia. These findings revealed alterations in the gut microbiota of METH users, and these alterations may play a role in psychotic syndrome and cognitive impairment. Although the mechanisms behind the links between these disorders and METH abuse are unknown, the relationships may indicate similarities in the pathogenesis of psychosis induced by METH abuse and other causes, providing a new paradigm for addiction and METH use disorder treatment. Nature Publishing Group UK 2021-09-13 /pmc/articles/PMC8437956/ /pubmed/34518605 http://dx.doi.org/10.1038/s41598-021-97548-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yang, Yongde Yu, Xuan Liu, Xuebing Liu, Guangya Zeng, Kuan Wang, Gang Altered fecal microbiota composition in individuals who abuse methamphetamine |
title | Altered fecal microbiota composition in individuals who abuse methamphetamine |
title_full | Altered fecal microbiota composition in individuals who abuse methamphetamine |
title_fullStr | Altered fecal microbiota composition in individuals who abuse methamphetamine |
title_full_unstemmed | Altered fecal microbiota composition in individuals who abuse methamphetamine |
title_short | Altered fecal microbiota composition in individuals who abuse methamphetamine |
title_sort | altered fecal microbiota composition in individuals who abuse methamphetamine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8437956/ https://www.ncbi.nlm.nih.gov/pubmed/34518605 http://dx.doi.org/10.1038/s41598-021-97548-1 |
work_keys_str_mv | AT yangyongde alteredfecalmicrobiotacompositioninindividualswhoabusemethamphetamine AT yuxuan alteredfecalmicrobiotacompositioninindividualswhoabusemethamphetamine AT liuxuebing alteredfecalmicrobiotacompositioninindividualswhoabusemethamphetamine AT liuguangya alteredfecalmicrobiotacompositioninindividualswhoabusemethamphetamine AT zengkuan alteredfecalmicrobiotacompositioninindividualswhoabusemethamphetamine AT wanggang alteredfecalmicrobiotacompositioninindividualswhoabusemethamphetamine |