Genetic approaches to understanding human obesity

被引:132
作者
Ramachandrappa, Shwetha [1 ]
Farooqi, I. Sadaf [1 ]
机构
[1] Univ Cambridge, Metab Res Labs, Inst Metab Sci, Addenbrookes Hosp, Cambridge CB2 0QQ, England
关键词
EARLY-ONSET OBESITY; BODY-MASS INDEX; CONGENITAL LEPTIN DEFICIENCY; BARDET-BIEDL-SYNDROME; PRADER-WILLI-SYNDROME; MELANOCYTE-STIMULATING HORMONE; CENTRAL MELANOCORTIN SYSTEM; MORBID-OBESITY; FTO GENE; NEUROTROPHIC FACTOR;
D O I
10.1172/JCI46044
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Obesity and its associated comorbidities represent one of the biggest public health challenges facing the world today. The heritability of body weight is high, and genetic variation plays a major role in determining the interindividual differences in susceptibility or resistance to the obesogenic environment. Here we discuss how genetic studies in humans have contributed to our understanding of the central pathways that govern energy homeostasis. We discuss how the arrival of technological advances such as next-generation sequencing will result in a major acceleration in the pace of gene discovery. The study of patients harboring these genetic variants has informed our understanding of the molecular and physiological pathways involved in energy homeostasis. We anticipate that future studies will provide the framework for the development of a more rational targeted approach to the prevention and treatment of genetically susceptible individuals.
引用
收藏
页码:2080 / 2086
页数:7
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