肥胖是遗传性疾病吗?

T. Duran, Hasanain Akram Zainalbden Zainalbden, N. Koçak
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引用次数: 0

摘要

肥胖是一种复杂的疾病,在世界范围内对所有民族人口都有不利的影响。遗传、环境和生活方式是该病的病因。与该疾病相关的遗传贡献通常分为两种类型:表现严重肥胖的单基因综合征和常见肥胖的多基因模型。单基因突变可导致中枢和外周食欲控制机制的改变而导致严重的肥胖。候选基因和全基因组关联研究已经鉴定出9个与孟德尔型肥胖相关的基因位点和58个与多基因型肥胖相关的基因位点。这些基因座只解释了肥胖遗传的一小部分,还有许多基因有待鉴定。多种多态性与表观遗传修饰的相互作用为常见肥胖开辟了新的研究领域。因此,至今仍是一个谜。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Is obesity genetic disease
Obesity is a complex disease that has unfavorable impacts for all ethnic populations in worldwide. Genetics, environment and lifestyle are among aetiological factors of this disease. Genetic contribution associated with this disease is generally classified into 2 types: monogenic syndromes that display severe obesity, and the polygenic model of common obesity. Single-gene mutations can cause severe obesity resulting from alteration in central and peripheral appetite control mechanisms. Candidate gene and genome-wide association studies have led to the identification of nine loci associated with Mendelian forms of obesity and 58 loci contributing to polygenic obesity. These loci explain a small fraction of the heritability for obesity and many genes remain to be identified. The interaction of several polymorphisms and epigenetic modifications open a new research field for common obesity. As a result, still remains to be a mystery.
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