Nutrition & Metabolism · 2018 · 18 citations · 45 references
Life SciencesNutritionNutritional SciencesEpigeneticsGene ExpressionHuman NutritionEpigenetic BiomarkersMicronutrient SupplementationMicrorna BiologyMicrorna-mediated RegulationVitamin PhysiologyWeight ManagementDietary EpigeneticsEnergy-restricted DietsEpigenetic Regulation By MicronutrientsMicrorna EpigeneticsMicrorna In MetabolismMicrorna-mediated Epigenetic ControlNutritional EpigeneticsPromoter Methylation
BACKGROUND: promoter DNA methylation in overweight women. METHODS: = 44) who ingested synthetic vitamin E (all-rac-α-tocopherol), natural source vitamin E (RRR-rac-α-tocopherol) or placebo capsules and were followed up for a period of 8 weeks. Supplemented groups also received dietary guidance for an energy-restricted diet. An additional group that received no supplementation and did not follow an energy-restricted diet was also followed up. The intervention effect was evaluated by DNA methylation levels (quantitative real-time PCR assay) and anthropometric and biochemical variables (fasting plasma glucose, haemoglobin A1C, insulin, and vitamin E). RESULTS: < 0.05) were observed in the natural source vitamin E group after intervention. Increased fasting plasma glucose was observed in the synthetic vitamin E group, despite the significant reduction of anthropometric variables compared to the other groups. CONCLUSIONS: promoter region and reduced haemoglobin A1C in overweight women following an energy-restricted diet. These results provide novel information about the influence of vitamin E on DNA methylation. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02922491. Registered 4 October, 2016.
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