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历史人口学与长寿遗传学:回到未来。

Historical demography and longevity genetics: Back to the future.

机构信息

Department of Molecular Epidemiology, Leiden University, Albinusdreef 2, 2333 ZA Leiden, The Netherlands.

Department of Family and Consumer Studies, Population Sciences, Huntsman Cancer Institute, University of Utah, 225 S. 1400 E. Rm 228, Salt Lake City, United States.

出版信息

Ageing Res Rev. 2017 Sep;38:28-39. doi: 10.1016/j.arr.2017.06.005. Epub 2017 Jul 5.

Abstract

Research into the genetic component of human longevity can provide important insights in mechanisms that may protect against age-related diseases and multi-morbidity. Thus far only a limited number of robust longevity loci have been detected in either candidate or genome wide association studies. One of the issues in these genetic studies is the definition of the trait being either lifespan, including any age at death or longevity, i.e. survival above a diverse series of thresholds. Likewise heritability and segregation research have conflated lifespan with longevity. The heritability of lifespan estimated across most studies has been rather low. Environmental factors have not been sufficiently investigated and the total amount of genetic variance contributing to longevity has not been estimated in sufficiently well-defined and powered studies. Up to now, genetic longevity studies lack the required insights into the nature and size of the genetic component and the optimal strategies for meta-analysis and subject selection for Next Generation Sequencing efforts. Historical demographic data containing deep genealogical information may help in estimating the best definition and heritability for longevity, its transmission patterns in multi-generational datasets and may allow relevant additive and modifying environmental factors such as socio-economic status, geographical background, exposure to environmental effects, birth order, and number of children to be included. In this light historical demographic data may be very useful for identifying lineages in human populations that are worth investigating further by geneticists.

摘要

对人类长寿的遗传因素的研究可以为可能预防与年龄相关的疾病和多种疾病的机制提供重要的见解。迄今为止,在候选或全基因组关联研究中仅检测到了有限数量的稳健的长寿基因座。这些遗传研究中的一个问题是将特征定义为寿命,包括任何死亡年龄或长寿,即超过一系列不同阈值的存活。同样,遗传性和分离研究将寿命与长寿混淆了。大多数研究中估计的寿命遗传性相当低。环境因素尚未得到充分研究,并且在充分定义和有力的研究中尚未估计出对长寿有贡献的遗传方差总量。到目前为止,遗传长寿研究缺乏对遗传成分的性质和大小以及荟萃分析和下一代测序工作的主题选择的最佳策略的必要了解。包含深入系谱信息的历史人口数据可能有助于估计长寿的最佳定义和遗传性,其在多代数据集的传播模式,并可能允许包括相关的加性和修饰性环境因素,如社会经济地位、地理背景、暴露于环境影响、出生顺序和子女数量。从这个角度来看,历史人口数据对于识别人类群体中的谱系非常有用,遗传学家可能会进一步对这些谱系进行研究。

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