Metabolic Profile Reflects Stages of Fibrosis in Patients with Non-Alcoholic Fatty Liver Disease

Author:

Jambulingam Nila1,Forlano Roberta1ORCID,Preston Benjamin1ORCID,Mullish Benjamin H.1ORCID,Portone Greta1,Baheer Yama1,Yee Michael2,Goldin Robert D.3,Thursz Mark R.1ORCID,Manousou Pinelopi1

Affiliation:

1. Liver Unit, Division of Digestive Diseases, Department of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London W2 1NY, UK

2. Section of Endocrinology and Metabolic Medicine, St Mary’s Hospital, Imperial College NHS Trust, London W2 1NY, UK

3. Department of Cellular Pathology, Faculty of Medicine, Imperial College London, London W2 1NY, UK

Abstract

Nonalcoholic fatty liver disease (NAFLD) is a leading cause of chronic liver disease worldwide, with fibrosis stage being the main predictor for clinical outcomes. Here, we present the metabolic profile of NAFLD patients with regards to fibrosis progression. We included all consecutive new referrals for NAFLD services between 2011 and 2019. Demographic, anthropometric and clinical features and noninvasive markers of fibrosis were recorded at baseline and at follow-up. Significant and advanced fibrosis were defined using liver stiffness measurement (LSM) as LSM ≥ 8.1 kPa and LSM ≥ 12.1 kPa, respectively. Cirrhosis was diagnosed either histologically or clinically. Fast progressors of fibrosis were defined as those with delta stiffness ≥ 1.03 kPa/year (25% upper quartile of delta stiffness distribution). Targeted and untargeted metabolic profiles were analysed on fasting serum samples using Proton nuclear magnetic resonance (1H NMR). A total of 189 patients were included in the study; 111 (58.7%) underwent liver biopsy. Overall, 11.1% patients were diagnosed with cirrhosis, while 23.8% were classified as fast progressors. A combination of metabolites and lipoproteins could identify the fast fibrosis progressors (AUROC 0.788, 95% CI: 0.703–0.874, p < 0.001) and performed better than noninvasive markers. Specific metabolic profiles predict fibrosis progression in patients with nonalcoholic fatty liver disease. Algorithms combining metabolites and lipids could be integrated in the risk-stratification of these patients.

Funder

National Institute of Health Research (NIHR) Imperial Biomedical Research Centre

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Reference29 articles.

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2. Design and validation of a histological scoring system for nonalcoholic fatty liver disease;Kleiner;Hepatology,2005

3. Fibrosis Stage Is the Strongest Predictor for Dis-ease-Specific Mortality in NAFLD After Up to 33Years of Follow-Up;Ekstedt;Hepatology,2015

4. EASL Clinical Practice Guidelines on non-invasive tests for evaluation of liver disease severity and prognosis—2021 update;Berzigotti;J. Hepatol.,2021

5. National Institute for Health and Care Excellence (2023, January 10). Non-Alcoholic Fatty Liver Disease (NAFLD): Assessment and Management NG49. Available online: https://www.nice.org.uk/guidance/ng49.

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