4.7 Article

Effects of lifestyle interventions on epigenetic signatures of liver fat: Central randomized controlled trial

Journal

LIVER INTERNATIONAL
Volume 41, Issue 9, Pages 2101-2111

Publisher

WILEY
DOI: 10.1111/liv.14916

Keywords

Diet; DNA‐ methylation; genetic variation; nonalcoholic fatty liver disease; physical activity

Funding

  1. Free State of Saxony
  2. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [209933838-SFB 1052]
  3. German Diabetes Association
  4. Deutsches Zentrum fur Diabetesforschung
  5. Israel Science Foundation (ISF), Israel Ministry of Science and Technology [3-13604]
  6. Dr Robert C. and Veronica Atkins Research Foundation

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In the CENTRAL trial, diverse liver fat dynamics were observed in response to different dietary interventions. Epigenetic mechanisms and genetic factors contribute to the variation in intrahepatic fat levels and development of NAFLD. However, long-term lifestyle interventions may lead to epigenetic remodeling and changes in DNA methylation patterns associated with IHF.
Background and Aims In the CENTRAL trial context, we found diverse liver fat dynamics in response to different dietary interventions. Epigenetic mechanisms may contribute to the intraindividual variation. Moreover, genetic factors are involved in developing nonalcoholic fatty-liver disease (NAFLD), a disease reflected by an increase in intrahepatic fat (IHF). In this exploratory analysis, we primarily aimed to examine the effect of lifestyle interventions on DNA-methylation of NAFLD related genes associated with IHF. Methods For 120 participants from the CENTRAL trial, an 18-month regimen of either low-fat (LF) or Mediterranean-low carbohydrate (MED/LC) diets, with or without physical activity (PA+/PA-), was instructed. Magnetic resonance imaging was used to measure IHF%, which was analysed for association with CpG specific DNA-methylation levels of 41 selected candidate genes. Single-nucleotide polymorphisms known to be associated with NAFLD within the studied genes were genotyped by TaqMan assays. Results At baseline, participants (92% men; body mass index = 30.2 kg/m(2)) had mean IHF of 10.7% (59% NAFLD). Baseline-IHF% was inversely correlated with DNA-methylation at individual CpGs within AC074286.1, CRACR2A, A2MP1, FARP1 (P < .05 for all multivariate models). FARP1 rs9584805 showed association with IHF, with the prevalence of NAFLD and baseline methylation level of the CpG site (cg00071727) associated with IHF%. Following 18-month lifestyle intervention, differential DNA-methylation patterns were observed between diets at cg14335324 annotated to A2MP1 (P = .04, LF vs. MED/LC), and differential DNA-methylation between PA groups within AC074286.1, CRACR2A, and FARP1 CpGs (P < .05 for all, PA-vs. PA+). Conclusions This study suggests epigenetic markers for IHF and potential epigenetic remodeling after long-term lifestyle interventions.

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