Risk assessment with gut microbiome and metabolite markers in NAFLD development

Author:

Leung Howell1ORCID,Long Xiaoxue2ORCID,Ni Yueqiong12ORCID,Qian Lingling2,Nychas Emmanouil1ORCID,Siliceo Sara Leal1ORCID,Pohl Dennis34ORCID,Hanhineva Kati567ORCID,Liu Yan89ORCID,Xu Aimin8910ORCID,Nielsen Henrik B.3,Belda Eugeni11ORCID,Clément Karine11ORCID,Loomba Rohit12,Li Huating2ORCID,Jia Weiping2ORCID,Panagiotou Gianni189ORCID

Affiliation:

1. Systems Biology and Bioinformatics Unit, Leibniz Institute for Natural Product Research and Infection Biology–Hans Knöll Institute, Beutenbergstraße 11A, 07745 Jena, Germany.

2. 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.

3. Clinical Microbiomics, Fruebjergvej 3, 2100 Copenhagen, Denmark.

4. Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kemitorvet, Building 220, 2800 Kgs. Lyngby, Denmark.

5. Department of Life Technologies, Food Chemistry and Food Development Unit, University of Turku, 20014 Turku, Finland.

6. Department of Biology and Biological Engineering, Division of Food and Nutrition Science, Chalmers University of Technology, 412 96 Gothenburg, Sweden.

7. School of Medicine, Institute of Public Health and Clinical Nutrition, University of Eastern Finland, 70211 Kuopio, Finland.

8. The State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong SAR, China.

9. Department of Medicine, The University of Hong Kong, Hong Kong SAR, China.

10. Department of Pharmacology and Pharmacy, The University of Hong Kong, Hong Kong SAR, China.

11. Sorbonne Université, INSERM, NutriOmics Research Unit, Nutrition Department, Pitié-Salpêtrière Hospital, Assistance Publique-Hôpitaux de Paris, 75013 Paris, France.

12. NAFLD Research Center, Department of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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