Relationship between BsmI polymorphism and VDR gene methylation profile, gender, metabolic profile, oxidative stress, and inflammation in adolescents

• Published in: Nutrición hospitalaria : organo oficial de la Sociedad Española de Nutrición Parenteral y Enteral Vol. 38; no. 5; pp. 911 - 918
• Main Authors: Lacerda de Lucena, Lavoisiana, Silva, Alexandre Sérgio, Nascimento, Rayner Anderson Ferreira do, Persuhn, Darlene Camati, Neves, Juliana Padilha Ramos, Costa, Maria José Carvalho, Queiroz, Dayana Joyce Marques, de Lima, Rafaela Lira Formiga Covalcanti, Ataíde de Lima, Raquel Patrícia, de Paiva, Maria Paula, Francis Paulo de Oliveira, Naila, Gonçalves, Maria da Conceição Rodrigues
• Format: Journal Article
• Language: English
• Published: Spain Grupo Arán 13-10-2021
• Subjects: Adolescent; Female; Humans; Inflammation - genetics; Inflammation - prevention & control; Male; Metabolome - genetics; Methylation; Nutrition & Dietetics; Oxidative Stress - genetics; Polymorphism, Genetic - genetics; Receptors, Calcitriol - drug effects; Receptors, Calcitriol - genetics; Sex Factors; Polimorfismos. Metilación del ADN. Vitamina D. Gen VDR; Vitamin D; Gen VDR; Metilación del ADN; DNA methylation; Polymorphisms; VDR gene; Polimorfismos; Vitamina D
• ISSN: 0212-1611; 1699-5198; 1699-5198
• DOI: 10.20960/nh.03383

Background: the biological activity of vitamin D depends on the activity of its receptor or VDR. On the other hand, the activity of this receptor is influenced by its state of methylation. The objective of this study was to verify if the BsmI polymorphism of the VDR gene influences its methylation profile in adolescents. Secondly, it was to verify if the status of some metabolic factors (oxidative stress, inflammation, lipid profile, and glycemia) in the serum, and gender-adjusted vitamin D levels are independent factors with an influence on the VDR methylation profile. Methods and results: the study included 198 adolescents of both sexes, aged 15-19 years, who underwent testing for VDR gene methylation polymorphisms, serum vitamin D levels, and metabolic, oxidative stress, and systemic inflammation markers. It was observed that the BB genotype was less methylated than the other groups (26.1 % versus 30.3 %, and 29.3 % for Bb and bb, respectively), although without statistical differences between them. The odds ratio indicated a protection of 13 % (partially methylated) for vitamin D status, while alpha glycols increased the risk ratio (of being partially methylated) by 3 %. MDA was protective at a 28 % chance of risk that adolescents with higher levels of lipid peroxidation would be hypomethylated. Conclusion: we conclude that the methylation profile of the VDR gene is not influenced by the different BsmI polymorphism genotypes, and that serum vitamin D and serum markers of oxidative stress and inflammation can modulate this profile.