Cargando…
Causal effects of gut microbiome on autoimmune liver disease: a two-sample Mendelian randomization study
BACKGROUND: Epidemiological studies have indicated a potential link between the gut microbiome and autoimmune liver disease (AILD) such as autoimmune hepatitis (AIH), primary biliary cholangitis (PBC), and primary sclerosing cholangitis (PSC). The relationship between the gut microbiome and autoimmu...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548566/ https://www.ncbi.nlm.nih.gov/pubmed/37789337 http://dx.doi.org/10.1186/s12920-023-01670-0 |
_version_ | 1785115294934499328 |
---|---|
author | Fu, Yugang Li, Jiacheng Zhu, Yingying Chen, Chong Liu, Jing Gu, Simin Zheng, Yiyuan Li, Yong |
author_facet | Fu, Yugang Li, Jiacheng Zhu, Yingying Chen, Chong Liu, Jing Gu, Simin Zheng, Yiyuan Li, Yong |
author_sort | Fu, Yugang |
collection | PubMed |
description | BACKGROUND: Epidemiological studies have indicated a potential link between the gut microbiome and autoimmune liver disease (AILD) such as autoimmune hepatitis (AIH), primary biliary cholangitis (PBC), and primary sclerosing cholangitis (PSC). The relationship between the gut microbiome and autoimmune liver disease is still uncertain due to confounding variables. In our study, we aim to shed light on this relationship by employing a two-sample Mendelian randomization approach. METHODS: We conducted a two-sample Mendelian randomization (MR) study using the R package "TwoSampleMR". The exposure data consisted of genetic variants associated with 194 bacterial traits obtained from the MiBioGen consortium. Summary statistics for AILD were obtained from the GWAS Catalog website. Furthermore, a series of sensitivity analyses were performed to validate the initial MR results. RESULTS: There were two, four and three bacteria traits associated with an increased risk of AIH. PBC, and PSC respectively. In contrast, there were five, two and five bacteria traits associated with a decreased risk for AIH, PBC and PSC. Notably, the genus_Clostridium_innocuum_group showed a negative association with AIH (OR = 0.67, 95% CI: 0.49–0.93), and the genus_Actinomyces was found to be genetically associated with a decreased risk of PSC (OR = 0.62, 95% CI: 0.42–0.90). CONCLUSIONS: Our study identified the causal impact of specific bacterial features on the risk of AILD subtypes. Particularly, the genus_Clostridium_innocuum_group and the genus_Actinomyces demonstrated significant protective effects against AIH and PSC respectively. These findings provide further support for the potential use of targeted probiotics in the management of AILD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01670-0. |
format | Online Article Text |
id | pubmed-10548566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105485662023-10-05 Causal effects of gut microbiome on autoimmune liver disease: a two-sample Mendelian randomization study Fu, Yugang Li, Jiacheng Zhu, Yingying Chen, Chong Liu, Jing Gu, Simin Zheng, Yiyuan Li, Yong BMC Med Genomics Research BACKGROUND: Epidemiological studies have indicated a potential link between the gut microbiome and autoimmune liver disease (AILD) such as autoimmune hepatitis (AIH), primary biliary cholangitis (PBC), and primary sclerosing cholangitis (PSC). The relationship between the gut microbiome and autoimmune liver disease is still uncertain due to confounding variables. In our study, we aim to shed light on this relationship by employing a two-sample Mendelian randomization approach. METHODS: We conducted a two-sample Mendelian randomization (MR) study using the R package "TwoSampleMR". The exposure data consisted of genetic variants associated with 194 bacterial traits obtained from the MiBioGen consortium. Summary statistics for AILD were obtained from the GWAS Catalog website. Furthermore, a series of sensitivity analyses were performed to validate the initial MR results. RESULTS: There were two, four and three bacteria traits associated with an increased risk of AIH. PBC, and PSC respectively. In contrast, there were five, two and five bacteria traits associated with a decreased risk for AIH, PBC and PSC. Notably, the genus_Clostridium_innocuum_group showed a negative association with AIH (OR = 0.67, 95% CI: 0.49–0.93), and the genus_Actinomyces was found to be genetically associated with a decreased risk of PSC (OR = 0.62, 95% CI: 0.42–0.90). CONCLUSIONS: Our study identified the causal impact of specific bacterial features on the risk of AILD subtypes. Particularly, the genus_Clostridium_innocuum_group and the genus_Actinomyces demonstrated significant protective effects against AIH and PSC respectively. These findings provide further support for the potential use of targeted probiotics in the management of AILD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-023-01670-0. BioMed Central 2023-10-03 /pmc/articles/PMC10548566/ /pubmed/37789337 http://dx.doi.org/10.1186/s12920-023-01670-0 Text en © The Author(s) 2023 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Fu, Yugang Li, Jiacheng Zhu, Yingying Chen, Chong Liu, Jing Gu, Simin Zheng, Yiyuan Li, Yong Causal effects of gut microbiome on autoimmune liver disease: a two-sample Mendelian randomization study |
title | Causal effects of gut microbiome on autoimmune liver disease: a two-sample Mendelian randomization study |
title_full | Causal effects of gut microbiome on autoimmune liver disease: a two-sample Mendelian randomization study |
title_fullStr | Causal effects of gut microbiome on autoimmune liver disease: a two-sample Mendelian randomization study |
title_full_unstemmed | Causal effects of gut microbiome on autoimmune liver disease: a two-sample Mendelian randomization study |
title_short | Causal effects of gut microbiome on autoimmune liver disease: a two-sample Mendelian randomization study |
title_sort | causal effects of gut microbiome on autoimmune liver disease: a two-sample mendelian randomization study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548566/ https://www.ncbi.nlm.nih.gov/pubmed/37789337 http://dx.doi.org/10.1186/s12920-023-01670-0 |
work_keys_str_mv | AT fuyugang causaleffectsofgutmicrobiomeonautoimmuneliverdiseaseatwosamplemendelianrandomizationstudy AT lijiacheng causaleffectsofgutmicrobiomeonautoimmuneliverdiseaseatwosamplemendelianrandomizationstudy AT zhuyingying causaleffectsofgutmicrobiomeonautoimmuneliverdiseaseatwosamplemendelianrandomizationstudy AT chenchong causaleffectsofgutmicrobiomeonautoimmuneliverdiseaseatwosamplemendelianrandomizationstudy AT liujing causaleffectsofgutmicrobiomeonautoimmuneliverdiseaseatwosamplemendelianrandomizationstudy AT gusimin causaleffectsofgutmicrobiomeonautoimmuneliverdiseaseatwosamplemendelianrandomizationstudy AT zhengyiyuan causaleffectsofgutmicrobiomeonautoimmuneliverdiseaseatwosamplemendelianrandomizationstudy AT liyong causaleffectsofgutmicrobiomeonautoimmuneliverdiseaseatwosamplemendelianrandomizationstudy |