Wang Tsu-Nai, Huang Meng-Chuan, Chang Wen-Tsan, Ko Albert Min-Shan, Tsai Eing-Mei, Liu Chih-Shan, Lee Chien-Hung, Ko Ying-Chin
Faculty of Public Health, Kaohsiung Medical University, Kaohsiung, Taiwan.
Obesity (Silver Spring). 2006 Feb;14(2):183-7. doi: 10.1038/oby.2006.23.
We examined the genetic associations of the G-2548A polymorphism in the promoter of the leptin (LEP) gene and the Gln223Arg (Q223R) polymorphism of the leptin receptor (LEPR) gene with obesity. Two hundred twenty-six obese aboriginal subjects (BMI > or = 27 kg/m2) and 182 aboriginal subjects with normal weight (BMI < 25 kg/m2) participated in this study. The polymorphisms of LEP G-2548A and LEPR Q223R were genotyped by polymerase chain reaction/restriction fragment length polymorphism, and their anthropometric characteristics were measured. Levels of leptin, triglycerides, and cholesterol were measured after overnight fasting. We found that the frequencies of the LEP G/G homozygote (22.6%) with Mendelian recessive (chi2 = 7.89, p = 0.005) and codominant (chi2 = 7.93, p = 0.02) models to be higher in the extremely obese subjects (BMI > or = 35 kg/m2) than in normal weight subjects (6.9%) but not in moderately obese subjects (35 > BMI > or = 27 kg/m2). There was no difference in genotypic frequency of the LEPR Q223R polymorphism between the extreme obese and control groups. We suggest that the LEP -2548 G/G homozygote plays a genetic recessive role in the development of extreme obesity in Taiwanese aborigines.
我们研究了瘦素(LEP)基因启动子中G-2548A多态性以及瘦素受体(LEPR)基因的Gln223Arg(Q223R)多态性与肥胖的遗传关联。226名肥胖原住民受试者(BMI≥27kg/m²)和182名体重正常的原住民受试者(BMI<25kg/m²)参与了本研究。通过聚合酶链反应/限制性片段长度多态性对LEP G-2548A和LEPR Q223R的多态性进行基因分型,并测量其人体测量学特征。过夜禁食后测量瘦素、甘油三酯和胆固醇水平。我们发现,在极度肥胖受试者(BMI≥35kg/m²)中,LEP G/G纯合子的频率(22.6%)在孟德尔隐性模型(χ² = 7.89,p = 0.005)和共显性模型(χ² = 7.93,p = 0.02)下高于体重正常的受试者(6.9%),但在中度肥胖受试者(35>BMI≥27kg/m²)中并非如此。极端肥胖组和对照组之间LEPR Q223R多态性的基因型频率没有差异。我们认为,LEP -2548 G/G纯合子在台湾原住民极端肥胖的发生中起遗传隐性作用。