一种新的高度透的肥胖形式,由于染色体16p11.2上的缺失
R G Walters1, S Jacquemont, A Valsesia
1Section of Genomic Medicine, Imperial College London, London W12 0NN, UK.
Nature
|February 5, 2010
概括
在16p11.2的罕见遗传缺失与严重肥胖有很强的联系,挑战了常见变异理论. 研究极端肥胖病例有助于发现导致遗传性的罕见遗传因素.
科学领域:
- 遗传学 是一个遗传学.
- 公共卫生 公共卫生
- 肥胖问题研究研究
背景情况:
- 肥胖是一个全球性的健康问题,受到环境和遗传学的影响.
- 全基因组关联研究 (GWAS) 确定了许多与肥胖相关的单核酸多态,但解释了遗传性很少.
- "常见疾病,常见变体"假设越来越受到质疑.
研究的目的:
- 研究罕见遗传变异在严重肥胖中的作用.
- 确定导致肥胖"遗传性缺失"的遗传因素.
- 探索研究极端现象型对遗传发现的实用性.
主要方法:
- 在31名肥胖和认知缺陷的受试者中分析了16p11.2删除.
- 在来自16053名欧洲人的GWAS数据中发现了19个类似的删除.
- 病态肥胖病例与健康对照之间的删除频率的比较.
主要成果:
- 在16p11.2的异构缺失在0.7%的病态肥胖病例中被发现 (OR=43.0,P=6.4x10^-8).
- 这些删除在健康的非肥胖对照中不存在.
- 具有强烈影响的罕见变异在肥胖等常见疾病中很重要.
结论:
- 罕见的变异,如16p11.2删除,显著促进肥胖遗传性.
- 研究具有极端表型的队列是发现罕见变异的有力策略.
- 将极端表型研究与人口队伍结合起来,可以进一步揭示对复杂特征的遗传贡献.
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