Luo Wenshu, Chen Fengmei, Guo Zhirong, Wu Ming, Zhou Zhengyuan, Yao Xingjuan
a Changzhou Center for Disease Control and Prevention , Changzhou , Jiangsu , PR China .
b Suzhou Health College , Suzhou , Jiangsu , PR China .
Ann Hum Biol. 2016;43(1):67-72. doi: 10.3109/03014460.2015.1023847. Epub 2015 Jun 15.
Peroxisome proliferator-activated receptor (PPAR) gene plays an important role in obesity and PPAR δ protein is a potent inhibitor; however, few previous studies have focused on this gene.
To investigate the association of haplotypes of PPAR δ gene rs2016520 and rs9794 with abnormal weight (BMI ≥ 24 kg/m(2)) and abdominal obesity (WC ≥ 90 cm for males and ≥ 80 cm for females) in a Chinese Han population.
In total, 820 subjects (270 men, 550 women) were randomly selected from the PMMJS cohort population and no individuals were related. rs2016520 and rs9794 were detected by TaqMan fluorescence probe. Hardy-Weinberg equilibrium (HWE) was used to detect genotype typing errors by Fisher's exact test. Linkage disequilibrium (LD) between polymorphisms was estimated by using SHEsis. Two PPAR δ SNPs (rs2016520 and rs9794) were analysed by using the logistic regression model.
After adjustment for covariates, the haplotype containing the rs1026520-C and rs9794-C alleles was associated with a statistically significant decreased risk of obesity (OR = 0.64; 95% CI = 0.48-0.84, p = 0.0015). Coincidentally, the haplotype containing the rs1026520-C and rs9794-C alleles was also associated with a statistically decreased risk of abdominal obesity after covariate adjustment (OR = 0.59, 95% CI = 0.45-0.77, p < 0.001).
C-C haplotype, constructed from rs2016520 and rs9794 alleles, showed a significant protective effect for both abnormal weight and abdominal obesity.
过氧化物酶体增殖物激活受体(PPAR)基因在肥胖中起重要作用,PPARδ蛋白是一种有效的抑制剂;然而,以往很少有研究关注该基因。
在中国汉族人群中,研究PPARδ基因rs2016520和rs9794单倍型与体重异常(BMI≥24kg/m²)及腹型肥胖(男性腰围≥90cm,女性腰围≥80cm)的关联。
从PMMJS队列人群中随机选取820名受试者(男性270名,女性550名),且无个体间存在亲缘关系。采用TaqMan荧光探针检测rs2016520和rs9794。通过Fisher精确检验,运用哈迪-温伯格平衡(HWE)检测基因分型错误。使用SHEsis估计多态性之间的连锁不平衡(LD)。采用逻辑回归模型分析两个PPARδ单核苷酸多态性(rs2016520和rs9794)。
校正协变量后,包含rs1026520-C和rs9794-C等位基因的单倍型与肥胖风险显著降低相关(OR=0.64;95%CI=0.48-0.84,p=0.0015)。巧合的是,校正协变量后,包含rs1026520-C和rs9794-C等位基因的单倍型与腹型肥胖风险降低也具有统计学意义(OR=0.59,95%CI=0.45-0.77,p<0.001)。
由rs2016520和rs9794等位基因构建的C-C单倍型对体重异常和腹型肥胖均显示出显著的保护作用。