Title of article
Genetics of human obesity
Author/Authors
Philippe Boutin، نويسنده , , Philippe Froguel، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2001
Pages
14
From page
391
To page
404
Abstract
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.
Keywords
obesity , genetics , leptin , Leptin receptor , POMC , Positional cloning , multifactorial disease , MC4R , genome-wide scans , susceptibility genes for obesity , linkage studies , association studies , linkage disequilibrium.
Journal title
Best Practice and Research Clinical Endocrinology and Metabolism
Serial Year
2001
Journal title
Best Practice and Research Clinical Endocrinology and Metabolism
Record number
465830
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