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Effects of lifestyle interventions on epigenetic signatures of liver fat: Central randomized controlled trial
Author(s) -
Yaskolka Meir Anat,
Keller Maria,
Müller Luise,
Bernhart Stephan H.,
Tsaban Gal,
Zelicha Hila,
Rinott Ehud,
Kaplan Alon,
Gepner Yftach,
Shelef Ilan,
Schwarzfuchs Dan,
Ceglarek Uta,
Stadler Peter,
Blüher Matthias,
Stumvoll Michael,
Kovacs Peter,
Shai Iris
Publication year - 2021
Publication title -
liver international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.873
H-Index - 110
eISSN - 1478-3231
pISSN - 1478-3223
DOI - 10.1111/liv.14916
Subject(s) - dna methylation , epigenetics , cpg site , context (archaeology) , methylation , nonalcoholic fatty liver disease , medicine , body mass index , biology , endocrinology , fatty liver , bioinformatics , genetics , gene , disease , gene expression , paleontology
Abstract 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.