*** TEST ***
Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

Regional distribution of body fat in relation to DNA methylation within the LPL, ADIPOQ and PPARγ promoters in subcutaneous adipose tissue

[thumbnail of Article] PDF (Article) - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
195kB
[thumbnail of Supplementary Table] Other (Supplementary Table)
10kB

Item Type:Article
Title:Regional distribution of body fat in relation to DNA methylation within the LPL, ADIPOQ and PPARγ promoters in subcutaneous adipose tissue
Creators Name:Drogan, D., Boeing, H., Janke, J., Schmitt, B., Zhou, Y., Walter, J., Pischon, T. and Tierling, S.
Abstract:Obesity may be related to differential DNA methylation and thus to differential expression of key genes in adipose tissue metabolism, such as LPL, ADIPOQ and PPARγ. Using subcutaneous adipose tissue (SAT) from 59 individuals of the European Prospective Investigation into Cancer and Nutrition-Potsdam study, we performed quantitative DNA methylation analysis within the promoters of LPL (LPL-CG1 and -CG2), ADIPOQ (ADIPOQ-CG1 and-CG2) and PPARγ (PPARγ-CG1). We then studied DNA methylation in relation to SAT gene expression, body composition measured using whole-body magnetic resonance imaging, body mass index (BMI), waist circumference (WC) and long-term changes in BMI and WC. For LPL-CG1 and LPL-CG2, higher methylation levels were associated with lower LPL expression, but with higher past WC gain. LPL-CG1 was also positively associated with BMI, WC, and visceral and subcutaneous fat mass. ADIPOQ-CG1 or -CG2 methylation exhibited no association with ADIPOQ expression or with anthropometric parameters. PPARγ-CG1 methylation was significantly higher in individuals with higher visceral fat mass. Among the investigated sites, LPL-CG1 methylation showed the strongest association with gene expression and regional body fat distribution, thereby possibly linking the degree of obesity with major metabolic processes in SAT.
Source:Nutrition & Diabetes
ISSN:2044-4052
Publisher:Nature Publishing Group
Volume:5
Page Range:e168
Date:6 July 2015
Official Publication:https://doi.org/10.1038/nutd.2015.19
PubMed:View item in PubMed

Repository Staff Only: item control page

Downloads

Downloads per month over past year

Open Access
MDC Library