» Articles » PMID: 38668319

Lipidome Changes Associated with a Diet-Induced Reduction in Hepatic Fat Among Adolescent Boys with Metabolic Dysfunction-Associated Steatotic Liver Disease

Overview
Journal Metabolites
Publisher MDPI
Date 2024 Apr 26
PMID 38668319
Authors
Affiliations
Soon will be listed here.
Abstract

Little is known about lipid changes that occur in the setting of metabolic-dysfunction-associated steatotic liver disease (MASLD) regression. We previously reported improvements in hepatic steatosis, de novo lipogenesis (DNL), and metabolomic profiles associated with oxidative stress, inflammation, and selected lipid metabolism in 40 adolescent boys (11-16 y) with hepatic steatosis ≥5% (98% meeting the definition of MASLD). Participants were randomized to a low-free-sugar diet (LFSD) (n = 20) or usual diet (n = 20) for 8 weeks. Here, we employed untargeted/targeted lipidomics to examine lipid adaptations associated with the LFSD and improvement of hepatic steatosis. Our LC-MS/MS analysis revealed decreased triglycerides (TGs), diacylglycerols (DGs), cholesteryl esters (ChE), lysophosphatidylcholine (LPC), and phosphatidylcholine (PC) species with the diet intervention ( < 0.05). Network analysis demonstrated significantly lower levels of palmitate-enriched TG species post-intervention, mirroring the previously shown reduction in DNL in response to the LFSD. Targeted oxylipins analysis revealed a decrease in the abundance of 8-isoprostane and 14,15-DiHET and an increase in 8,9-DiHET ( < 0.05). Overall, we observed reductions in TGs, DGs, ChE, PC, and LPC species among participants in the LFSD group. These same lipids have been associated with MASLD progression; therefore, our findings may indicate normalization of key biological processes, including lipid metabolism, insulin resistance, and lipotoxicity. Additionally, our targeted oxylipins assay revealed novel changes in eicosanoids, suggesting improvements in oxidative stress. Future studies are needed to elucidate the mechanisms of these findings and prospects of these lipids as biomarkers of MASLD regression.

Citing Articles

Oxylipins Derived from PUFAs in Cardiometabolic Diseases: Mechanism of Actions and Possible Nutritional Interactions.

Agagunduz D, Yesildemir O, Kocyigit E, Kocak T, Ozen Unaldi B, Ayakdas G Nutrients. 2024; 16(22).

PMID: 39599599 PMC: 11597274. DOI: 10.3390/nu16223812.

References
1.
Cohen C, Huneault H, Accardi C, Jones D, Liu K, Maner-Smith K . Metabolome × Microbiome Changes Associated with a Diet-Induced Reduction in Hepatic Fat among Adolescent Boys. Metabolites. 2023; 13(3). PMC: 10053986. DOI: 10.3390/metabo13030401. View

2.
Maner-Smith K, Goll J, Khadka M, Jensen T, Colucci J, Gelber C . Alterations in the Human Plasma Lipidome in Response to Tularemia Vaccination. Vaccines (Basel). 2020; 8(3). PMC: 7564507. DOI: 10.3390/vaccines8030414. View

3.
Langfelder P, Horvath S . WGCNA: an R package for weighted correlation network analysis. BMC Bioinformatics. 2008; 9:559. PMC: 2631488. DOI: 10.1186/1471-2105-9-559. View

4.
Bakdash J, Marusich L . Repeated Measures Correlation. Front Psychol. 2017; 8:456. PMC: 5383908. DOI: 10.3389/fpsyg.2017.00456. View

5.
Cantero I, Abete I, Del Bas J, Caimari A, Arola L, Zulet M . Changes in lysophospholipids and liver status after weight loss: the RESMENA study. Nutr Metab (Lond). 2018; 15:51. PMC: 6050739. DOI: 10.1186/s12986-018-0288-5. View