Targeted metabolomics reveals bioactive inflammatory mediators from gut into blood circulation in children with NAFLD

Abstract Altered gut metabolites are important for the inflammatory progression in children with NAFLD. Fecal and plasma samples were collected from 145 subjects including 53 non-alcoholic fatty liver (NAFL), 39 nonalcoholic steatohepatitis (NASH) and 53 obese controls. We performed G350 targeted in...

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Main Authors: Miyang Luo, Jiayou Luo, Atipatsa C. Kaminga, Jia Wei, Wen Dai, Yan Zhong, Ningan Xu, Xiongwei Li, Haixiang Zhou, Xiongfeng Pan
Format: Article
Language:English
Published: Nature Portfolio 2025-07-01
Series:npj Biofilms and Microbiomes
Online Access:https://doi.org/10.1038/s41522-025-00706-w
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author Miyang Luo
Jiayou Luo
Atipatsa C. Kaminga
Jia Wei
Wen Dai
Yan Zhong
Ningan Xu
Xiongwei Li
Haixiang Zhou
Xiongfeng Pan
author_facet Miyang Luo
Jiayou Luo
Atipatsa C. Kaminga
Jia Wei
Wen Dai
Yan Zhong
Ningan Xu
Xiongwei Li
Haixiang Zhou
Xiongfeng Pan
author_sort Miyang Luo
collection DOAJ
description Abstract Altered gut metabolites are important for the inflammatory progression in children with NAFLD. Fecal and plasma samples were collected from 145 subjects including 53 non-alcoholic fatty liver (NAFL), 39 nonalcoholic steatohepatitis (NASH) and 53 obese controls. We performed G350 targeted integrative metabolomics using high performance liquid chromatography mass spectrometry for fecal and plasma analysis of NAFL, NASH, and obese children. We found 9 metabolites involved in metabolic reprogramming of inflammation in NAFLD, such as lipid, carbohydrate, amino acid metabolism, and TCA cycle pathway. Moreover, 7 inflammation-related metabolites could discriminate NAFLD severity by machine learning model. This study identified three novel elevated inflammatory pathogenic metabolites and the relationship between increased inflammation, may be involved in TLR5/MYD88/NFκB pathway. These findings reveal that specific inflammatory metabolites entering the blood circulation from the gut are associated with disease severity and inflammatory pathogenesis in children with NAFLD.
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publishDate 2025-07-01
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spelling doaj-art-a00f16d5318d481a93aab9ddc608edb22025-08-20T03:03:38ZengNature Portfolionpj Biofilms and Microbiomes2055-50082025-07-0111111310.1038/s41522-025-00706-wTargeted metabolomics reveals bioactive inflammatory mediators from gut into blood circulation in children with NAFLDMiyang Luo0Jiayou Luo1Atipatsa C. Kaminga2Jia Wei3Wen Dai4Yan Zhong5Ningan Xu6Xiongwei Li7Haixiang Zhou8Xiongfeng Pan9Department of Epidemiology and Health Statistics, Department of Maternal and Child Health, Xiangya School of Public Health, Central South UniversityDepartment of Epidemiology and Health Statistics, Department of Maternal and Child Health, Xiangya School of Public Health, Central South UniversityDepartment of Epidemiology and Health Statistics, Department of Maternal and Child Health, Xiangya School of Public Health, Central South UniversityDepartment of Epidemiology and Health Statistics, Department of Maternal and Child Health, Xiangya School of Public Health, Central South UniversityDepartment of Epidemiology and Health Statistics, Department of Maternal and Child Health, Xiangya School of Public Health, Central South UniversityInstitute of Children Health, Hunan Children’s HospitalInstitute of Children Health, Hunan Children’s HospitalCenter for Disease Control and Prevention of NingxiangCenter for Disease Control and Prevention of NingxiangPediatrics Research Institute of Hunan Province, Hunan Children’s Hospital, The Affiliated Children’s Hospital of Xiangya School of Medicine, Central South UniversityAbstract Altered gut metabolites are important for the inflammatory progression in children with NAFLD. Fecal and plasma samples were collected from 145 subjects including 53 non-alcoholic fatty liver (NAFL), 39 nonalcoholic steatohepatitis (NASH) and 53 obese controls. We performed G350 targeted integrative metabolomics using high performance liquid chromatography mass spectrometry for fecal and plasma analysis of NAFL, NASH, and obese children. We found 9 metabolites involved in metabolic reprogramming of inflammation in NAFLD, such as lipid, carbohydrate, amino acid metabolism, and TCA cycle pathway. Moreover, 7 inflammation-related metabolites could discriminate NAFLD severity by machine learning model. This study identified three novel elevated inflammatory pathogenic metabolites and the relationship between increased inflammation, may be involved in TLR5/MYD88/NFκB pathway. These findings reveal that specific inflammatory metabolites entering the blood circulation from the gut are associated with disease severity and inflammatory pathogenesis in children with NAFLD.https://doi.org/10.1038/s41522-025-00706-w
spellingShingle Miyang Luo
Jiayou Luo
Atipatsa C. Kaminga
Jia Wei
Wen Dai
Yan Zhong
Ningan Xu
Xiongwei Li
Haixiang Zhou
Xiongfeng Pan
Targeted metabolomics reveals bioactive inflammatory mediators from gut into blood circulation in children with NAFLD
npj Biofilms and Microbiomes
title Targeted metabolomics reveals bioactive inflammatory mediators from gut into blood circulation in children with NAFLD
title_full Targeted metabolomics reveals bioactive inflammatory mediators from gut into blood circulation in children with NAFLD
title_fullStr Targeted metabolomics reveals bioactive inflammatory mediators from gut into blood circulation in children with NAFLD
title_full_unstemmed Targeted metabolomics reveals bioactive inflammatory mediators from gut into blood circulation in children with NAFLD
title_short Targeted metabolomics reveals bioactive inflammatory mediators from gut into blood circulation in children with NAFLD
title_sort targeted metabolomics reveals bioactive inflammatory mediators from gut into blood circulation in children with nafld
url https://doi.org/10.1038/s41522-025-00706-w
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