Cargando…
Associations of the gut microbiome with hepatic adiposity in the Multiethnic Cohort Adiposity Phenotype Study
Nonalcoholic fatty liver disease (NAFLD) is a risk factor for liver cancer and prevalence varies by ethnicity. Along with genetic and lifestyle factors, the gut microbiome (GM) may contribute to NAFLD and its progression to advanced liver disease. Our cross-sectional analysis assessed the associatio...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425768/ https://www.ncbi.nlm.nih.gov/pubmed/34491886 http://dx.doi.org/10.1080/19490976.2021.1965463 |
_version_ | 1783749904588341248 |
---|---|
author | Hullar, Meredith A. J. Jenkins, Isaac C. Randolph, Timothy W. Curtis, Keith R. Monroe, Kristine R. Ernst, Thomas Shepherd, John A. Stram, Daniel O. Cheng, Iona Kristal, Bruce S. Wilkens, Lynne R. Franke, Adrian Le Marchand, Loic Lim, Unhee Lampe, Johanna W. |
author_facet | Hullar, Meredith A. J. Jenkins, Isaac C. Randolph, Timothy W. Curtis, Keith R. Monroe, Kristine R. Ernst, Thomas Shepherd, John A. Stram, Daniel O. Cheng, Iona Kristal, Bruce S. Wilkens, Lynne R. Franke, Adrian Le Marchand, Loic Lim, Unhee Lampe, Johanna W. |
author_sort | Hullar, Meredith A. J. |
collection | PubMed |
description | Nonalcoholic fatty liver disease (NAFLD) is a risk factor for liver cancer and prevalence varies by ethnicity. Along with genetic and lifestyle factors, the gut microbiome (GM) may contribute to NAFLD and its progression to advanced liver disease. Our cross-sectional analysis assessed the association of the GM with hepatic adiposity among African American, Japanese American, White, Latino, and Native Hawaiian participants in the Multiethnic Cohort. We used MRI to measure liver fat and determine nonalcoholic fatty liver disease (NAFLD) status (n = 511 cases) in 1,544 participants, aged 60–77 years, with 12–53% overall adiposity (BMI of 17.8–46.2 kg/m(2)). The GM was measured by 16S rRNA gene sequencing and, on a subset, by metagenomic sequencing. Alpha diversity was lower overall with NAFLD and in certain ethnicities (African Americans, Whites, and Latinos). In models regressing genus on NAFLD status, 62 of 149 genera (40%) exhibited a significant interaction between NAFLD and ethnicity stratified analysis found 69 genera significantly associated with NAFLD in at least one ethnic group. No single genus was significantly associated with NAFLD across all ethnicities. In contrast, the same bacterial metabolic pathways were over-represented in participants with NAFLD regardless of ethnicity. Imputed secondary bile acid and carbohydrate pathways were associated with NAFLD, the latter of which was corroborated by metagenomics, although different genera in different ethnicities were associated with these pathways. Overall, we found that NAFLD was associated with altered bacterial composition and metabolism, and that bacterial endotoxin, assessed by plasma lipopolysaccharide binding protein (LBP), may mediate liver fat-associated systemic inflammation in a manner that seems to vary by ethnicity. |
format | Online Article Text |
id | pubmed-8425768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-84257682021-09-09 Associations of the gut microbiome with hepatic adiposity in the Multiethnic Cohort Adiposity Phenotype Study Hullar, Meredith A. J. Jenkins, Isaac C. Randolph, Timothy W. Curtis, Keith R. Monroe, Kristine R. Ernst, Thomas Shepherd, John A. Stram, Daniel O. Cheng, Iona Kristal, Bruce S. Wilkens, Lynne R. Franke, Adrian Le Marchand, Loic Lim, Unhee Lampe, Johanna W. Gut Microbes Research Paper Nonalcoholic fatty liver disease (NAFLD) is a risk factor for liver cancer and prevalence varies by ethnicity. Along with genetic and lifestyle factors, the gut microbiome (GM) may contribute to NAFLD and its progression to advanced liver disease. Our cross-sectional analysis assessed the association of the GM with hepatic adiposity among African American, Japanese American, White, Latino, and Native Hawaiian participants in the Multiethnic Cohort. We used MRI to measure liver fat and determine nonalcoholic fatty liver disease (NAFLD) status (n = 511 cases) in 1,544 participants, aged 60–77 years, with 12–53% overall adiposity (BMI of 17.8–46.2 kg/m(2)). The GM was measured by 16S rRNA gene sequencing and, on a subset, by metagenomic sequencing. Alpha diversity was lower overall with NAFLD and in certain ethnicities (African Americans, Whites, and Latinos). In models regressing genus on NAFLD status, 62 of 149 genera (40%) exhibited a significant interaction between NAFLD and ethnicity stratified analysis found 69 genera significantly associated with NAFLD in at least one ethnic group. No single genus was significantly associated with NAFLD across all ethnicities. In contrast, the same bacterial metabolic pathways were over-represented in participants with NAFLD regardless of ethnicity. Imputed secondary bile acid and carbohydrate pathways were associated with NAFLD, the latter of which was corroborated by metagenomics, although different genera in different ethnicities were associated with these pathways. Overall, we found that NAFLD was associated with altered bacterial composition and metabolism, and that bacterial endotoxin, assessed by plasma lipopolysaccharide binding protein (LBP), may mediate liver fat-associated systemic inflammation in a manner that seems to vary by ethnicity. Taylor & Francis 2021-09-07 /pmc/articles/PMC8425768/ /pubmed/34491886 http://dx.doi.org/10.1080/19490976.2021.1965463 Text en © 2021 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Hullar, Meredith A. J. Jenkins, Isaac C. Randolph, Timothy W. Curtis, Keith R. Monroe, Kristine R. Ernst, Thomas Shepherd, John A. Stram, Daniel O. Cheng, Iona Kristal, Bruce S. Wilkens, Lynne R. Franke, Adrian Le Marchand, Loic Lim, Unhee Lampe, Johanna W. Associations of the gut microbiome with hepatic adiposity in the Multiethnic Cohort Adiposity Phenotype Study |
title | Associations of the gut microbiome with hepatic adiposity in the Multiethnic Cohort Adiposity Phenotype Study |
title_full | Associations of the gut microbiome with hepatic adiposity in the Multiethnic Cohort Adiposity Phenotype Study |
title_fullStr | Associations of the gut microbiome with hepatic adiposity in the Multiethnic Cohort Adiposity Phenotype Study |
title_full_unstemmed | Associations of the gut microbiome with hepatic adiposity in the Multiethnic Cohort Adiposity Phenotype Study |
title_short | Associations of the gut microbiome with hepatic adiposity in the Multiethnic Cohort Adiposity Phenotype Study |
title_sort | associations of the gut microbiome with hepatic adiposity in the multiethnic cohort adiposity phenotype study |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425768/ https://www.ncbi.nlm.nih.gov/pubmed/34491886 http://dx.doi.org/10.1080/19490976.2021.1965463 |
work_keys_str_mv | AT hullarmeredithaj associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT jenkinsisaacc associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT randolphtimothyw associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT curtiskeithr associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT monroekristiner associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT ernstthomas associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT shepherdjohna associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT stramdanielo associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT chengiona associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT kristalbruces associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT wilkenslynner associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT frankeadrian associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT lemarchandloic associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT limunhee associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy AT lampejohannaw associationsofthegutmicrobiomewithhepaticadiposityinthemultiethniccohortadiposityphenotypestudy |