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
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
e0261555Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
Références
Lancet. 2018 Nov 24;392(10161):2299-2312
pubmed: 30396512
J Hepatol. 2016 Jun;64(6):1388-402
pubmed: 27062661
J Card Fail. 2011 Sep;17(9):755-63
pubmed: 21872146
J Lipid Res. 2010 Jun;51(6):1344-53
pubmed: 20129912
FASEB J. 2007 Apr;21(4):1227-32
pubmed: 17218538
J Affect Disord. 2020 Jun 15;271:39-48
pubmed: 32312696
Brain Commun. 2021 Apr 19;3(2):fcab084
pubmed: 33997784
J Clin Psychiatry. 2020 Nov 17;82(1):
pubmed: 33211910
Dialogues Clin Neurosci. 2018 Mar;20(1):63-73
pubmed: 29946213
Clin Chem. 2015 May;61(5):714-23
pubmed: 25779987
Aliment Pharmacol Ther. 2019 Sep;50(5):590-598
pubmed: 31328300
BMC Gastroenterol. 2014 Jun 10;14:106
pubmed: 24916323
Hepatology. 2016 Jul;64(1):73-84
pubmed: 26707365
J Proteome Res. 2015 Aug 7;14(8):3322-35
pubmed: 26088811
Int J Mol Sci. 2014 Apr 11;15(4):6184-223
pubmed: 24733068
Hepatol Commun. 2020 Jun 22;4(9):1293-1301
pubmed: 32923833
Diabetes Care. 2012 May;35(5):1171-80
pubmed: 22517938
Gen Hosp Psychiatry. 2010 Nov-Dec;32(6):583-9
pubmed: 21112449
Sci Rep. 2016 Mar 23;6:23441
pubmed: 27006086
Mol Psychiatry. 2021 Aug;26(8):4265-4276
pubmed: 31959849
Nutrients. 2019 Dec 07;11(12):
pubmed: 31817857
Mol Psychiatry. 2019 Jan;24(1):18-33
pubmed: 29453413
J Gastroenterol Hepatol. 2015 Jun;30(6):1009-14
pubmed: 25619308
Liver Int. 2013 Aug;33(7):1062-70
pubmed: 23560860
BMC Bioinformatics. 2011 Mar 17;12:77
pubmed: 21414208
Hepatol Commun. 2018 Aug 06;2(8):893-905
pubmed: 30094401
J Crohns Colitis. 2018 Nov 15;12(11):1326-1337
pubmed: 30016408
Am J Clin Nutr. 2021 Sep 1;114(3):1028-1038
pubmed: 34100082
Biol Psychiatry. 2020 Mar 1;87(5):409-418
pubmed: 31635762
J Clin Psychiatry. 2006 Oct;67(10):1536-41
pubmed: 17107244
Acta Neuropsychiatr. 2016 Jun;28(3):173-8
pubmed: 26512905