Boutin P, Froguel P
CNRS-Institute of Biology of Lille, Pasteur Institute of Lille, France.
Best Pract Res Clin Endocrinol Metab. 2001 Sep;15(3):391-404. doi: 10.1053/beem.2001.0153.
Obesity is a multifactorial condition. Environmental risk factors related to a sedentary life-style and unlimited access to food apply constant pressure in subjects with a genetic predisposition to gain weight. The fact that genetic defects can result in human obesity has been unequivocally established over the past 3 years with the identification of the genetic defects responsible for different monogenic forms of human obesity: the leptin, leptin receptor, pro-opiomelanocortin, pro-hormone convertase-1 and melanocortin-4 receptor genes. The common forms of obesity are, however, polygenic. The examination of specific genes for involvement in the susceptibility to common obesity has not yet yielded convincing results. Approaches involving the candidate genes and the positional cloning of major obesity-linked regions (state-of-the-art future prospects) will be discussed.
肥胖是一种多因素疾病。与久坐不动的生活方式以及无节制获取食物相关的环境风险因素,对具有体重增加遗传易感性的个体持续施加压力。在过去3年里,随着导致人类不同单基因形式肥胖的遗传缺陷被确定,即瘦素、瘦素受体、阿黑皮素原、激素原转化酶-1和黑皮质素-4受体基因,遗传缺陷可导致人类肥胖这一事实已得到明确证实。然而,常见的肥胖形式是多基因的。对参与常见肥胖易感性的特定基因进行检测尚未得出令人信服的结果。将讨论涉及候选基因以及主要肥胖相关区域定位克隆的方法(最先进的未来前景)。