Suppr超能文献

肿瘤坏死因子-α启动子甲基化作为减肥反应的预测生物标志物。

TNF-alpha promoter methylation as a predictive biomarker for weight-loss response.

作者信息

Campión Javier, Milagro Fermin I, Goyenechea Estibaliz, Martínez J Alfredo

机构信息

Department of Food Sciences, Physiology and Toxicology, University of Navarra, Navarra, Spain.

出版信息

Obesity (Silver Spring). 2009 Jun;17(6):1293-7. doi: 10.1038/oby.2008.679. Epub 2009 Feb 19.

Abstract

Tumor necrosis factor-alpha (TNF-alpha) is a proinflammatory cytokine which is commonly elevated in obese subjects and whose promoter is susceptible to be regulated by cytosine methylation. The aim of this research was to analyze whether epigenetic regulation of human TNF-alpha promoter by cytosine methylation could be involved in the predisposition to lose body weight after following a balanced hypocaloric diet. Twenty-four patients (12 women/12 men) with excessive body weight-for-height (BMI: 30.5+/-0.32 kg/m2; age: 34+/-4 years old) followed an 8-week energy-restricted diet. Blood mononuclear cell DNA, isolated before the nutritional intervention, was treated with bisulfite and a region of TNF-alpha gene promoter (from -360 to +50 bp) was sequenced. Obese men with successful weight loss (>or=5% of initial body weight) showed lower levels of total TNF-alpha promoter methylation (r=0.74; P=0.021), especially in the positions -170 bp (r=0.75, P=0.005) and -120 bp (r=0.70, P=0.011). Baseline TNF-alpha circulating levels were positively associated with total promoter methylation (r=0.84, P=0.005) and methylation at position -245 bp (r=0.75, P=0.020). TNF-alpha promoter methylation could be a good inflammation marker predicting the hypocaloric diet-induced weight-loss, and constitutes a first step toward personalized nutrition based on epigenetic criteria.

摘要

肿瘤坏死因子-α(TNF-α)是一种促炎细胞因子,在肥胖个体中通常会升高,其启动子易受胞嘧啶甲基化调控。本研究的目的是分析胞嘧啶甲基化对人TNF-α启动子的表观遗传调控是否与在均衡低热量饮食后体重减轻的易感性有关。24例身高体重超标患者(12名女性/12名男性;体重指数:30.5±0.32kg/m²;年龄:34±4岁)接受了为期8周的能量限制饮食。在营养干预前分离的血液单核细胞DNA用亚硫酸氢盐处理,并对TNF-α基因启动子区域(从-360至+50bp)进行测序。体重成功减轻(≥初始体重的5%)的肥胖男性显示出较低水平的TNF-α启动子总甲基化(r=0.74;P=0.021),尤其是在-170bp(r=0.75,P=0.005)和-120bp(r=0.70,P=0.011)位置。基线TNF-α循环水平与启动子总甲基化(r=0.84,P=0.005)和-245bp位置的甲基化(r=0.75,P=0.020)呈正相关。TNF-α启动子甲基化可能是预测低热量饮食诱导体重减轻的良好炎症标志物,并且是基于表观遗传标准迈向个性化营养的第一步。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验