4.8 Article

Risk assessment with gut microbiome and metabolite markers in NAFLD development

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SCIENCE TRANSLATIONAL MEDICINE
卷 14, 期 648, 页码 -

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/scitranslmed.abk0855

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资金

  1. Marie Sklodowska-Curie Actions (MSCA) [H2020-MSCA-ITN-2018 813781]
  2. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [EXC 2051, 390713860]
  3. Hong Kong Research Grants Council/Area of Excellence [AoE/M/707-18]
  4. EU [E/HKU703/20]
  5. National Natural Science Foundation of China (NSFC)-NHMRC joint research grant [81561128016]
  6. Shanghai Municipal Key Clinical Specialty
  7. National Key Research and Development Program of China [2018YFA0800402]
  8. NSFC [81870598, 82022012]
  9. Two Hundred Program from Shanghai Jiao Tong University School of Medicine [20191830]
  10. Innovative Research Team of High-level Local Universities in Shanghai [SHSMU-ZDCX20212700]
  11. Assistance Publique Hopitaux de Paris (APHP) DGOS
  12. NCATS [5UL1TR001442]
  13. NIDDK [U01DK061734, U01DK130190, R01DK106419, R01DK121378, R01DK124318, P30DK120515]
  14. NHLBI [P01HL147835]
  15. NIAAA [U01AA029019]

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A growing body of evidence suggests that the gut microbiota plays a role in the pathogenesis of nonalcoholic fatty liver disease (NAFLD). This study found that machine learning models integrating microbial signatures were able to accurately classify individuals based on their NAFLD status and liver fat accumulation, outperforming other clinical models. These findings raise the possibility of using gut microbiota for early clinical warning of NAFLD development.
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.

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