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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
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