ARTÍCULO

TNF-alpha promoter methylation in peripheral white blood cells: Relationship with circulating TNFalpha, truncal fat and n-6 PUFA intake in young women

Autores: Hermsdorff, H.H.; Mansego Talavera, María Luisa; Campión Zabalza, Francisco Javier; Milagro Yoldi, Fermín Ignacio; Zulet Alzórriz, María de los Ángeles; Martínez Hernández, Alfredo
Título de la revista: CYTOKINE
ISSN: 1043-4666
Volumen: 64
Número: 1
Páginas: 265 - 271
Fecha de publicación: 2013
Resumen:
The aim of this article is to assess the potential relationships between TNFalpha gene promoter methylation in peripheral white blood cells and central adiposity (truncal fat), metabolic features and dietary fat intake. A group of 40 normal-weight young women (213y; BMI 21.01.7kg/m(2)) was included in this cross-sectional study. Anthropometric, biochemical and dietary data were assessed using validated procedures. DNA from white blood cells was isolated and 5-methylcytosine levels of the CpGs sites present in TNFalpha gene promoter (from -170 to +359 pb) were analyzed by Sequenom EpiTyper. Those women with high truncal fat (¿52.3%) showed lower 5-methylcytosine levels (P<0.05) in the site CpG13 (at position +207) and CpG19 (+317 pb) of the TNFalpha gene promoter when were compared to women with lower truncal adiposity. The methylation levels of CpG13 were also correlated with circulating TNFalpha levels, which were higher in those women with greater truncal adiposity. In a linear regression model, truncal fat, HDL-cholesterol, insulin, plasma TNFalpha, and daily n-6 PUFA intake explained the methylation levels of CpG13 site +207 by 48% and the average of CpG13 and CpG19 by 43% (P<0.001). In conclusion, women with higher truncal fat showed lower methylation levels of TNFalpha promoter in peripheral white blood cells and higher plasma TNFalpha concentrations. DNA methylation levels of TNFalpha promoter were associated with some metabolic features and with n-6 PUFA intake, suggesting a complex nutriepigenomic network in the regulation of this recognized pro-inflammatory marker.