Lagou Vasiliki, Scott Robert A, Manios Yannis, Chen Tun-Li Joshua, Wang Guan, Grammatikaki Evangelia, Kortsalioudaki Christine, Liarigkovinos Thodoris, Moschonis George, Roma-Giannikou Eleftheria, Pitsiladis Yannis P
Faculty of Biomedical and Life Sciences, Institute of Diet, Exercise and Lifestyle (IDEAL), University of Glasgow, Glasgow, UK.
Obesity (Silver Spring). 2008 Apr;16(4):913-8. doi: 10.1038/oby.2008.1. Epub 2008 Jan 31.
Peroxisome proliferator-activated receptor gamma (PPAR gamma) and peroxisome proliferator-activated receptor delta (PPAR delta) are promising candidate genes for obesity. Associations between adiposity-related phenotypes and genetic variation in PPAR gamma (Pro12Ala and C1431T), as well as PPAR delta (T+294C) were assessed in 2,102 Greek children aged 1-6 years, as part of a large-scale epidemiological study (Growth, Exercise and Nutrition Epidemiological Study In preSchoolers). In girls aged 3-4 years, the Ala12 allele was associated with higher mid-upper arm (P = 0.010) and hip (P = 0.005) circumferences, as well as subscapular (P = 0.008) and total skinfolds (P = 0.011) that explained 2.0, 3.7, 2.1, and 1.9% of the phenotypic variance, respectively, while the T1431 allele was associated with higher mean values for waist circumference (P = 0.018) and suprailiac skinfold (P = 0.017), genotype accounting for 1.6% of the variance in both phenotypes. No significant effects of PPAR delta T+294C polymorphism or the interaction of the PPAR delta and PPAR gamma variants on adiposity-related phenotypes were observed in any age group or gender. Haplotype-based analysis including both PPAR gamma polymorphisms revealed that in girls aged 3-4 years, the Ala-T haplotype was associated with higher waist (P = 0.014) and hip (P = 0.007) circumferences compared to the common Pro-C haplotype. The PPAR gamma Pro12Ala and C1431T polymorphisms are associated with increased adiposity during early childhood in a gender- and age-specific manner and independently of the PPAR delta T+294C polymorphism.
过氧化物酶体增殖物激活受体γ(PPARγ)和过氧化物酶体增殖物激活受体δ(PPARδ)是肥胖症很有前景的候选基因。作为一项大规模流行病学研究(学龄前儿童生长、运动与营养流行病学研究)的一部分,对2102名1至6岁的希腊儿童进行了肥胖相关表型与PPARγ(Pro12Ala和C1431T)以及PPARδ(T+294C)基因变异之间关联的评估。在3至4岁的女孩中,Ala12等位基因与较高的上臂中部(P = 0.010)和髋部(P = 0.005)周长以及肩胛下(P = 0.008)和总皮褶厚度(P = 0.011)相关,分别解释了表型变异的2.0%、3.7%、2.1%和1.9%,而T1431等位基因与较高的腰围平均值(P = 0.018)和髂上皮肤褶厚度(P = 0.017)相关,基因型在两种表型中占变异的1.6%。在任何年龄组或性别中均未观察到PPARδ T+294C多态性或PPARδ与PPARγ变异的相互作用对肥胖相关表型有显著影响。包括PPARγ两种多态性的单倍型分析显示,在3至4岁的女孩中,与常见的Pro-C单倍型相比,Ala-T单倍型与较高的腰围(P = 0.014)和髋部(P = 0.007)周长相关。PPARγ Pro12Ala和C1431T多态性以性别和年龄特异性方式且独立于PPARδ T+294C多态性与幼儿期肥胖增加相关。