Depressive symptoms in non-alcoholic fatty liver disease are identified by perturbed lipid and lipoprotein metabolism.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2022
Historique:
received: 26 07 2021
accepted: 06 12 2021
entrez: 6 1 2022
pubmed: 7 1 2022
medline: 17 2 2022
Statut: epublish

Résumé

Non-alcoholic fatty liver disease (NAFLD) and depression are common disorders and have bidirectional contributing relationships to metabolic syndrome. We aimed to determine whether a fasting serum signature of recent, self-reported depressive symptoms could be identified in a heterogeneous NAFLD cohort using nuclear magnetic resonance (NMR)-based metabolomics integrated with clinical chemistry. Serum nuclear magnetic resonance (NMR) metabolite profiles and corresponding clinical chemistry were compared between patients with depressive symptoms in the last 12-months (n = 81) and patients without recent depressive symptoms (n = 137 controls) using multivariate statistics. Orthogonal partial least squares discriminant analysis (OPLS-DA) of the biochemical and metabolomic data identified NAFLD patients with recent depression with a cross-validated accuracy of 61.5%, independent of age, sex, medication, and other comorbidities. This led to the development of a diagnostic algorithm with AUC 0.83 for future testing in larger clinical cohorts. Serum triglycerides, VLDL cholesterol, and the inflammatory biomarker GlycA were key metabolites increased in patients with recent depressive symptoms, while serum glutamine level was reduced. Here, serum NMR metabolite analysis provides a link between disturbed lipid metabolism, inflammation, and active mental health issues in NAFLD, irrespective of disease severity.

Identifiants

pubmed: 34990473
doi: 10.1371/journal.pone.0261555
pii: PONE-D-21-24239
pmc: PMC8735618
doi:

Substances chimiques

Biomarkers 0
Lipoproteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0261555

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Daniel E Radford-Smith (DE)

Department of Pharmacology, University of Oxford, Oxford, United Kingdom.
Department of Chemistry, University of Oxford, Oxford, United Kingdom.
Department of Psychiatry, Warneford Hospital, University of Oxford, Oxford, United Kingdom.

Preya J Patel (PJ)

Institute for Liver and Digestive Health, University College London, London, United Kingdom.
The Liver Unit, Newcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.

Katharine M Irvine (KM)

Centre for Liver Disease Research, The University of Queensland, Brisbane, Australia.
Mater Research, The University of Queensland, Brisbane, Australia.

Anthony Russell (A)

Department of Diabetes and Endocrinology, Princess Alexandra Hospital, Brisbane, Australia.
Centre for Health Services Research, The University of Queensland, Brisbane, Australia.

Dan Siskind (D)

School of Clinical Medicine, The University of Queensland, Woolloongabba, QLD, Australia.
Metro South Addiction and Mental Health Service, Woolloongabba, QLD, Australia.

Daniel C Anthony (DC)

Department of Pharmacology, University of Oxford, Oxford, United Kingdom.

Elizabeth E Powell (EE)

Centre for Liver Disease Research, The University of Queensland, Brisbane, Australia.
Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Australia.

Fay Probert (F)

Department of Chemistry, University of Oxford, Oxford, United Kingdom.

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