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Risk assessment with gut microbiome and metabolite markers in NAFLD development.
Leung, Howell; Long, Xiaoxue; Ni, Yueqiong; Qian, Lingling; Nychas, Emmanouil; Siliceo, Sara Leal; Pohl, Dennis; Hanhineva, Kati; Liu, Yan; Xu, Aimin; Nielsen, Henrik B; Belda, Eugeni; Clément, Karine; Loomba, Rohit; Li, Huating; Jia, Weiping; Panagiotou, Gianni.
Afiliação
  • Leung H; Systems Biology and Bioinformatics Unit, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute, Beutenbergstraße 11A, 07745 Jena, Germany.
  • Long X; Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai Diabetes Institute, Shanghai Clinical Center for Diabetes, Shanghai Key Laboratory of Diabetes Mellitus, 200233 Shanghai, China.
  • Ni Y; Systems Biology and Bioinformatics Unit, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute, Beutenbergstraße 11A, 07745 Jena, Germany.
  • Qian L; Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai Diabetes Institute, Shanghai Clinical Center for Diabetes, Shanghai Key Laboratory of Diabetes Mellitus, 200233 Shanghai, China.
  • Nychas E; Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai Diabetes Institute, Shanghai Clinical Center for Diabetes, Shanghai Key Laboratory of Diabetes Mellitus, 200233 Shanghai, China.
  • Siliceo SL; Systems Biology and Bioinformatics Unit, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute, Beutenbergstraße 11A, 07745 Jena, Germany.
  • Pohl D; Systems Biology and Bioinformatics Unit, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute, Beutenbergstraße 11A, 07745 Jena, Germany.
  • Hanhineva K; Clinical Microbiomics, Fruebjergvej 3, 2100 Copenhagen, Denmark.
  • Liu Y; Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kemitorvet, Building 220, 2800 Kgs. Lyngby, Denmark.
  • Xu A; Department of Life Technologies, Food Chemistry and Food Development Unit, University of Turku, 20014 Turku, Finland.
  • Nielsen HB; Department of Biology and Biological Engineering, Division of Food and Nutrition Science, Chalmers University of Technology, 412 96 Gothenburg, Sweden.
  • Belda E; School of Medicine, Institute of Public Health and Clinical Nutrition, University of Eastern Finland, 70211 Kuopio, Finland.
  • Clément K; The State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong SAR, China.
  • Loomba R; Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Li H; The State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong SAR, China.
  • Jia W; Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.
  • Panagiotou G; Department of Pharmacology and Pharmacy, The University of Hong Kong, Hong Kong SAR, China.
Sci Transl Med ; 14(648): eabk0855, 2022 06 08.
Article em En | MEDLINE | ID: mdl-35675435
ABSTRACT
A growing body of evidence suggests interplay between the gut microbiota and the pathogenesis of nonalcoholic fatty liver disease (NAFLD). However, the role of the gut microbiome in early detection of NAFLD is unclear. Prospective studies are necessary for identifying reliable, microbiome markers for early NAFLD. We evaluated 2487 individuals in a community-based cohort who were followed up 4.6 years after initial clinical examination and biospecimen sampling. Metagenomic and metabolomic characterizations using stool and serum samples taken at baseline were performed for 90 participants who progressed to NAFLD and 90 controls who remained NAFLD free at the follow-up visit. Cases and controls were matched for gender, age, body mass index (BMI) at baseline and follow-up, and 4-year BMI change. Machine learning models integrating baseline microbial signatures (14 features) correctly classified participants (auROCs of 0.72 to 0.80) based on their NAFLD status and liver fat accumulation at the 4-year follow up, outperforming other prognostic clinical models (auROCs of 0.58 to 0.60). We confirmed the biological relevance of the microbiome features by testing their diagnostic ability in four external NAFLD case-control cohorts examined by biopsy or magnetic resonance spectroscopy, from Asia, Europe, and the United States. Our findings raise the possibility of using gut microbiota for early clinical warning of NAFLD development.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatopatia Gordurosa não Alcoólica / Microbioma Gastrointestinal Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatopatia Gordurosa não Alcoólica / Microbioma Gastrointestinal Idioma: En Ano de publicação: 2022 Tipo de documento: Article