Role of interaction between variants in the PPARG and interleukin-6 genes on obesity related metabolic risk factors

被引:43
作者
Barbieri, M
Rizzo, MR
Papa, M
Acampora, R
De Angelis, L
Olivieri, F
Marchegiani, F
Franceschi, C
Paolisso, G
机构
[1] Univ Naples Federico II, Dept Geriatr Med & Metab Dis 2, Div Med Interna 6, I-80138 Naples, Italy
[2] Italian Natl Res Ctr Aging, I-60100 Ancona, Italy
[3] Univ Bologna, Dept Expt Pathol, I-40126 Bologna, Italy
关键词
PPARG; IL-6; gene polymorphism; insulin resistance; body mass index;
D O I
10.1016/j.exger.2005.05.004
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The combined effect of Peroxisome proliferator-activated receptor gamma (PPARG) Pro/Ala and interleukin-6 G174C gene variants, was evaluated in 429 Caucasian subjects in order to determine whether subjects carrying both variants were at different risk for obesity. In particular, the combined contribution of these two variants (both independent and interaction effects) to the total variation of obesity-related factors was estimated. All subjects were genotyped for codon 12 Pro/Ala locus variability and for the interleukin-6-174 C/G promoter polymorphism. Subjects with the Ala variant had significantly lower BMI, insulin resistance, triglyceride levels than those without. Furthermore, subjects with Ala variant had significantly lower IL-6 levels (0.88 +/- 0.9 vs 1.61 +/- 2.25 pg/ml; p = 0.041). In contrast, the IL6-C variant was significantly associated with lower plasma IL-6 and with lower total cholesterol levels but was not significantly associated with any other obesity risk factors. Indeed, subjects carrying both PPARG and IL-6 gene variants, had a clearly more favourable profile of obesity related risk factors than subjects with one variant, having Ala+/C+ carriers lower BMI (22.8 +/- 2.3 vs 24.14 +/- 1.9; f = 5.31; p < 0.005), insulin resistance (1.49 +/- 0.70 vs 2.13 +/- 0.92; f = 4.342; p = 0.038) and triglyceride levels (79.15 +/- 32.9 vs 98 +/- 6.73 mg/dl; f = 3.120; p < 0.005). These findings suggest that the effect of the two genetic variants on 'obesity related' factors is additive. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:599 / 604
页数:6
相关论文
共 44 条
[41]   Circulating interleukin-6 in relation to adiposity, insulin action, and insulin secretion [J].
Vozarova, B ;
Weyer, C ;
Hanson, K ;
Tataranni, PA ;
Bogardus, C ;
Pratley, RE .
OBESITY RESEARCH, 2001, 9 (07) :414-417
[42]   Chronic inflammation in fat plays a crucial role in the development of obesity-related insulin resistance [J].
Xu, HY ;
Barnes, GT ;
Yang, Q ;
Tan, Q ;
Yang, DS ;
Chou, CJ ;
Sole, J ;
Nichols, A ;
Ross, JS ;
Tartaglia, LA ;
Chen, H .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (12) :1821-1830
[43]   Molecular scanning of the human peroxisome proliferator activated receptor γ (hPPARγ) gene in diabetic Caucasians:: Identification of a Pro12Ala PPARγ2 missense mutation [J].
Yen, CJ ;
Beamer, BA ;
Negri, C ;
Silver, K ;
Brown, KA ;
Yarnall, DP ;
Burns, DK ;
Roth, J ;
Shuldiner, AR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 241 (02) :270-274
[44]   Selective disruption of PPARγ2 impairs the development of adipose tissue and insulin sensitivity [J].
Zhang, JF ;
Fu, MG ;
Cui, TX ;
Chen, X ;
Xu, KF ;
Zhong, W ;
Xiao, Y ;
Floyd, D ;
Liang, J ;
Li, E ;
Song, Q ;
Chen, YE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (29) :10703-10708