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Beyond the fourth wave of genome-wide obesity association studies

机译:超越第四波全基因组肥胖关联研究

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Obesity and related complications are major health burdens. Almost 700 million adults are currently obese globally and the prevalence is predicted to rise towards 2030. The sudden change of lifestyle with physical inactivity and excessive calorie intake undoubtedly have a major part of the epidemic development; however, some individuals seem to be more prone to be affected by an unhealthy lifestyle than others. Hence, genetic predisposition also has an essential role in determining disease susceptibility and response to lifestyle factors. Since the introduction of genome-wide association studies (GWAS), the success of identifying obesity susceptibility variants have increased, and a total of 32 variants have been identified associating genome-wide significantly with body mass index (BMI) and 18 with measures of fat distribution during four overall obesity GWAS waves. However, the immediate success of the GWAS approach has eased off, but the proportion of explained variance for BMI by the identified obesity variants remains low. This review suggests and discusses new initiatives to take GWAS of obesity to the next level, including gene–environment interactions as modulating/masking factors, low-frequent or rare variants and ways to address such analyses, and finally reflections about the applicability of epigenetic modifications when elucidating the genetic background of obesity.
机译:肥胖和相关并发症是主要的健康负担。目前,全球有将近7亿成年人肥胖,并且预计到2030年这一比例将上升。毫无运动能力的生活方式的突然改变和过多的卡路里摄入无疑是流行病发展的主要部分。但是,有些人似乎比其他人更容易受到不良生活方式的影响。因此,遗传易感性在确定疾病易感性和对生活方式因素的反应中也具有重要作用。自从引入全基因组关联研究(GWAS)以来,鉴定肥胖易感性变体的成功率不断提高,已鉴定出总共32个变体将全基因组显着与体重指数(BMI)相关联,将18个变体与脂肪测量相关联四个整体肥胖GWAS波的分布。然而,GWAS方法的立即成功已经减弱,但是通过识别出的肥胖症变异导致的BMI解释差异的比例仍然很低。这篇综述提出并讨论了将肥胖的GWAS提升到新水平的新举措,包括基因-环境相互作用作为调节/掩蔽因子,低频率或稀有变异以及解决此类分析的方法,最后对表观遗传修饰的适用性进行了反思在阐明肥胖症的遗传背景时。

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