Kramer Holly, Wu Xiaodong, Kan Donghui, Luke Amy, Zhu Xiaofeng, Adeyemo Adebowale, McKenzie Colin, Cooper Richard
Loyola Medical Center, Department of Preventive Medicine, 2160 First Avenue, Maywood, IL 60153, USA.
Obes Res. 2005 May;13(5):823-8. doi: 10.1038/oby.2005.94.
We examined the association between obesity and 13 angiotensin-converting enzyme (ACE) gene polymorphisms, including the presence (I) or absence (D) of an Alu element in intron 16 (I/D polymorphism), and performed haplotype analysis using data collected from participants of a community survey of hypertension among blacks living in Ibadan, Nigeria; Spanish Town, Jamaica; and Chicago, IL. Transmission distortion of ACE gene polymorphisms and haplotypes from heterozygous parents to affected offspring was examined in each study population. To estimate haplotypes, polymorphisms were divided into three groups based on their position on the ACE gene. No ACE gene polymorphism was consistently overtransmitted from parents to obese offspring among the three populations. However, the haplotype ACE1-ACE5 TACAT, located in the promoter region, was significantly overtransmitted from parents to obese offspring in both the U.S. and Nigerian populations. No haplotype was significantly overtransmitted from parents to obese offspring among the Jamaicans. In conclusion, we noted the overtransmission of a particular ACE gene promoter region haplotype from parents to obese offspring in two separate black populations. These data suggest that ACE gene polymorphisms may influence the development of weight gain.
我们研究了肥胖与13种血管紧张素转换酶(ACE)基因多态性之间的关联,包括第16内含子中Alu元件的存在(I)或缺失(D)(I/D多态性),并使用从尼日利亚伊巴丹、牙买加西班牙镇和伊利诺伊州芝加哥的黑人高血压社区调查参与者收集的数据进行单倍型分析。在每个研究人群中,检查了ACE基因多态性和单倍型从杂合子父母向受影响后代的传递扭曲情况。为了估计单倍型,根据多态性在ACE基因上的位置将其分为三组。在这三个人群中,没有ACE基因多态性从父母向肥胖后代持续过度传递。然而,位于启动子区域的单倍型ACE1-ACE5 TACAT在美国和尼日利亚人群中从父母向肥胖后代显著过度传递。在牙买加人中,没有单倍型从父母向肥胖后代显著过度传递。总之,我们注意到在两个不同的黑人种群中,特定的ACE基因启动子区域单倍型从父母向肥胖后代过度传递。这些数据表明,ACE基因多态性可能影响体重增加的发展。