Fructose Induced Endotoxemia in Pediatric Nonalcoholic Fatty Liver Disease

In preclinical studies of fructose-induced NAFLD, endotoxin appears to play an important role. We retrospectively examined samples from three pediatric cohorts (1) to investigate whether endotoxemia is associated with the presence of hepatic steatosis; (2) to evaluate postprandial endotoxin levels i...

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Main Authors: Jin, Ran, Willment, Andrew, Patel, Shivani S., Sun, Xiaoyan, Song, Ming, Mannery, Yanci O., Kosters, Astrid, McClain, Craig J., Vos, Miriam B.
Format: Online
Language:English
Published: Hindawi Publishing Corporation 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195259/
id pubmed-4195259
recordtype oai_dc
spelling pubmed-41952592014-10-19 Fructose Induced Endotoxemia in Pediatric Nonalcoholic Fatty Liver Disease Jin, Ran Willment, Andrew Patel, Shivani S. Sun, Xiaoyan Song, Ming Mannery, Yanci O. Kosters, Astrid McClain, Craig J. Vos, Miriam B. Research Article In preclinical studies of fructose-induced NAFLD, endotoxin appears to play an important role. We retrospectively examined samples from three pediatric cohorts (1) to investigate whether endotoxemia is associated with the presence of hepatic steatosis; (2) to evaluate postprandial endotoxin levels in response to fructose beverage in an acute 24-hour feeding challenge, and (3) to determine the change of fasting endotoxin amounts in a 4-week randomized controlled trial comparing fructose to glucose beverages in NAFLD. We found that adolescents with hepatic steatosis had elevated endotoxin levels compared to obese controls and that the endotoxin level correlated with insulin resistance and several inflammatory cytokines. In a 24-hour feeding study, endotoxin levels in NAFLD adolescents increased after fructose beverages (consumed with meals) as compared to healthy children. Similarly, endotoxin was significantly increased after adolescents consumed fructose beverages for 2 weeks and remained high although not significantly at 4 weeks. In conclusion, these data provide support for the concept of low level endotoxemia contributing to pediatric NAFLD and the possible role of fructose in this process. Further studies are needed to determine if manipulation of the microbiome or other methods of endotoxin reduction would be useful as a therapy for pediatric NAFLD. Hindawi Publishing Corporation 2014 2014-09-28 /pmc/articles/PMC4195259/ /pubmed/25328713 http://dx.doi.org/10.1155/2014/560620 Text en Copyright © 2014 Ran Jin et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Jin, Ran
Willment, Andrew
Patel, Shivani S.
Sun, Xiaoyan
Song, Ming
Mannery, Yanci O.
Kosters, Astrid
McClain, Craig J.
Vos, Miriam B.
spellingShingle Jin, Ran
Willment, Andrew
Patel, Shivani S.
Sun, Xiaoyan
Song, Ming
Mannery, Yanci O.
Kosters, Astrid
McClain, Craig J.
Vos, Miriam B.
Fructose Induced Endotoxemia in Pediatric Nonalcoholic Fatty Liver Disease
author_facet Jin, Ran
Willment, Andrew
Patel, Shivani S.
Sun, Xiaoyan
Song, Ming
Mannery, Yanci O.
Kosters, Astrid
McClain, Craig J.
Vos, Miriam B.
author_sort Jin, Ran
title Fructose Induced Endotoxemia in Pediatric Nonalcoholic Fatty Liver Disease
title_short Fructose Induced Endotoxemia in Pediatric Nonalcoholic Fatty Liver Disease
title_full Fructose Induced Endotoxemia in Pediatric Nonalcoholic Fatty Liver Disease
title_fullStr Fructose Induced Endotoxemia in Pediatric Nonalcoholic Fatty Liver Disease
title_full_unstemmed Fructose Induced Endotoxemia in Pediatric Nonalcoholic Fatty Liver Disease
title_sort fructose induced endotoxemia in pediatric nonalcoholic fatty liver disease
description In preclinical studies of fructose-induced NAFLD, endotoxin appears to play an important role. We retrospectively examined samples from three pediatric cohorts (1) to investigate whether endotoxemia is associated with the presence of hepatic steatosis; (2) to evaluate postprandial endotoxin levels in response to fructose beverage in an acute 24-hour feeding challenge, and (3) to determine the change of fasting endotoxin amounts in a 4-week randomized controlled trial comparing fructose to glucose beverages in NAFLD. We found that adolescents with hepatic steatosis had elevated endotoxin levels compared to obese controls and that the endotoxin level correlated with insulin resistance and several inflammatory cytokines. In a 24-hour feeding study, endotoxin levels in NAFLD adolescents increased after fructose beverages (consumed with meals) as compared to healthy children. Similarly, endotoxin was significantly increased after adolescents consumed fructose beverages for 2 weeks and remained high although not significantly at 4 weeks. In conclusion, these data provide support for the concept of low level endotoxemia contributing to pediatric NAFLD and the possible role of fructose in this process. Further studies are needed to determine if manipulation of the microbiome or other methods of endotoxin reduction would be useful as a therapy for pediatric NAFLD.
publisher Hindawi Publishing Corporation
publishDate 2014
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195259/
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