Literature DB >> 30197273

Effects of free omega-3 carboxylic acids and fenofibrate on liver fat content in patients with hypertriglyceridemia and non-alcoholic fatty liver disease: A double-blind, randomized, placebo-controlled study.

Jan Oscarsson1, Kristina Önnerhag2, Ulf Risérus3, Mattias Sundén4, Lars Johansson5, Per-Anders Jansson6, Linda Moris7, Peter M Nilsson2, Jan W Eriksson8, Lars Lind8.   

Abstract

BACKGROUND: Treatment with omega-3 fatty acids and fenofibrates reduces serum triglyceride levels, but few studies have compared the effect of these agents on liver fat.
OBJECTIVE: The aim of the EFFECT I trial (NCT02354976) was to determine the effects of free omega-3 carboxylic acids (OM-3CA) and fenofibrate on liver fat in overweight or obese individuals with non-alcoholic fatty liver disease and hypertriglyceridemia.
METHODS: Seventy-eight patients were randomized to receive oral doses of 4 g OM-3CA (n = 25), 200 mg fenofibrate (n = 27), or placebo (n = 26) for 12 weeks in a double-blind, parallel-group study. Liver proton density fat fraction (PDFF) and volume, pancreas volume, and adipose tissue volumes were assessed by magnetic resonance imaging.
RESULTS: Changes in liver PDFF at 12 weeks were not significantly different across treatment groups (relative changes from baseline: placebo, +4%; OM-3CA, -2%; and fenofibrate, +17%). The common PNPLA3 genetic polymorphism (I148M) did not significantly influence the effects of OM-3CA or fenofibrate on liver PDFF. Fenofibrate treatment significantly increased liver and pancreas volumes vs placebo treatment, and the changes in liver and pancreas volumes were positively correlated (rho 0.45, P = .02). Total liver fat volume increased significantly in patients using fenofibrate vs OM-3CA (+23% vs -3%, P = .04). Compared with OM-3CA, fenofibrate increased total liver fat and liver volume. Serum triglycerides decreased with OM-3CA (-26%, P = .02) and fenofibrate (-38%, P < .001) vs placebo. In contrast to OM-3CA, fenofibrate reduced plasma docosahexaenoic acid levels and increased plasma acetylcarnitine and butyrylcarnitine levels, estimated delta-9 desaturase activity and the concentration of urine F2-isoprostanes.
CONCLUSIONS: OM-3CA and fenofibrate reduced serum triglycerides but did not reduce liver fat. Fenofibrate increased total liver volume and total liver fat volume vs OM-3CA, indicating a complex effect of fenofibrate on human hepatic lipid metabolism.
Copyright © 2018 National Lipid Association. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cholesterol; Fatty liver disease; Lipoproteins; Liver; Non-alcoholic fatty liver disease; Omega-3 fatty acids; PPARs; Pancreas; Triglycerides

Mesh:

Substances:

Year:  2018        PMID: 30197273     DOI: 10.1016/j.jacl.2018.08.003

Source DB:  PubMed          Journal:  J Clin Lipidol        ISSN: 1876-4789            Impact factor:   4.766


  23 in total

Review 1.  Efficacy of Dietary Manipulations for Depleting Intrahepatic Triglyceride Content: Implications for the Management of Non-alcoholic Fatty Liver Disease.

Authors:  Karoline Sandby; Nina Rica Wium Geiker; Maria Dalamaga; Henning Grønbæk; Faidon Magkos
Journal:  Curr Obes Rep       Date:  2021-02-13

Review 2.  Targeted therapeutics and novel signaling pathways in non-alcohol-associated fatty liver/steatohepatitis (NAFL/NASH).

Authors:  Xiaohan Xu; Kyle L Poulsen; Lijuan Wu; Shan Liu; Tatsunori Miyata; Qiaoling Song; Qingda Wei; Chenyang Zhao; Chunhua Lin; Jinbo Yang
Journal:  Signal Transduct Target Ther       Date:  2022-08-13

Review 3.  Metabolic liver disease in diabetes - From mechanisms to clinical trials.

Authors:  Bedair Dewidar; Sabine Kahl; Kalliopi Pafili; Michael Roden
Journal:  Metabolism       Date:  2020-06-20       Impact factor: 8.694

Review 4.  Metabolic Targets in Nonalcoholic Fatty Liver Disease.

Authors:  William P Esler; Kendra K Bence
Journal:  Cell Mol Gastroenterol Hepatol       Date:  2019-04-18

5.  Absolute Quantification of Apolipoproteins Following Treatment with Omega-3 Carboxylic Acids and Fenofibrate Using a High Precision Stable Isotope-labeled Recombinant Protein Fragments Based SRM Assay.

Authors:  Andreas Hober; Fredrik Edfors; Maria Ryaboshapkina; Jonas Malmqvist; Louise Rosengren; Andrew J Percy; Lars Lind; Björn Forsström; Mathias Uhlén; Jan Oscarsson; Tasso Miliotis
Journal:  Mol Cell Proteomics       Date:  2019-10-07       Impact factor: 5.911

6.  Nutritional supplementation for nonalcohol-related fatty liver disease: a network meta-analysis.

Authors:  Oluyemi Komolafe; Elena Buzzetti; Audrey Linden; Lawrence Mj Best; Angela M Madden; Danielle Roberts; Thomas Jg Chase; Dominic Fritche; Suzanne C Freeman; Nicola J Cooper; Alex J Sutton; Elisabeth Jane Milne; Kathy Wright; Chavdar S Pavlov; Brian R Davidson; Emmanuel Tsochatzis; Kurinchi Selvan Gurusamy
Journal:  Cochrane Database Syst Rev       Date:  2021-07-19

7.  The PPAR pan-agonist tetradecylthioacetic acid promotes redistribution of plasma cholesterol towards large HDL.

Authors:  Thomas Lundåsen; Matteo Pedrelli; Bodil Bjørndal; Björn Rozell; Raoul V Kuiper; Lena Burri; Chiara Pavanello; Marta Turri; Jon Skorve; Rolf K Berge; Stefan E H Alexson; Veronika Tillander
Journal:  PLoS One       Date:  2020-03-16       Impact factor: 3.240

8.  Effects of Omega-3 Polyunsaturated Fatty Acid Supplementation on Non-Alcoholic Fatty Liver: A Systematic Review and Meta-Analysis.

Authors:  Cheng-Han Lee; Yun Fu; Shih-Jyun Yang; Ching-Chi Chi
Journal:  Nutrients       Date:  2020-09-11       Impact factor: 5.717

Review 9.  Peroxisome Proliferator-Activated Receptors and Their Novel Ligands as Candidates for the Treatment of Non-Alcoholic Fatty Liver Disease.

Authors:  Anne Fougerat; Alexandra Montagner; Nicolas Loiseau; Hervé Guillou; Walter Wahli
Journal:  Cells       Date:  2020-07-08       Impact factor: 6.600

10.  Efficacy of Dietary Supplements to Reduce Liver Fat.

Authors:  Brittanie Kilchoer; Anina Vils; Beatrice Minder; Taulant Muka; Marija Glisic; Lia Bally
Journal:  Nutrients       Date:  2020-07-31       Impact factor: 5.717

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