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衰老的进化理论与Gompertz相关参数问题。

Evolutionary theory of ageing and the problem of correlated Gompertz parameters.

作者信息

Burger Oskar, Missov Trifon I

机构信息

Max Planck Institute for Demographic Research, Konrad-Zuse-Str. 1, 18057, Rostock, Germany.

Max Planck Institute for Demographic Research, Konrad-Zuse-Str. 1, 18057, Rostock, Germany; Mathematical Demography, University of Rostock, Ulmenstr. 69, 18057 Rostock, Germany.

出版信息

J Theor Biol. 2016 Nov 7;408:34-41. doi: 10.1016/j.jtbi.2016.08.002. Epub 2016 Aug 5.

Abstract

The Gompertz mortality model is often used to evaluate evolutionary theories of ageing, such as the Medawar-Williams' hypothesis that high extrinsic mortality leads to faster ageing. However, fits of the Gompertz mortality model to data often find the opposite result that mortality is negatively correlated with the rate of ageing. This negative correlation has been independently discovered in several taxa and is known in actuarial studies of ageing as the Strehler-Mildvan correlation. We examine the role of mortality selection in determining late-life variation in susceptibility to death, which has been suggested to be the cause of this negative correlation. We demonstrate that fixed-frailty models that account for heterogeneity in frailty do not remove the correlation and that the correlation is an inherent statistical property of the Gompertz distribution. Linking actuarial and biological rates of ageing will continue to be a pressing challenge, but the Strehler-Mildvan correlation itself should not be used to diagnose any biological, physiological, or evolutionary process. These findings resolve some key tensions between theory and data that affect evolutionary and biological studies of ageing and mortality. Tests of evolutionary theories of ageing should include direct measures of physiological performance or condition.

摘要

冈珀茨死亡率模型常用于评估衰老的进化理论,比如梅达沃 - 威廉姆斯假说,即高外在死亡率会导致更快衰老。然而,将冈珀茨死亡率模型应用于数据时,常常得出相反的结果,即死亡率与衰老速率呈负相关。这种负相关已在多个分类群中独立发现,在衰老的精算研究中被称为斯特勒 - 米尔德万相关性。我们研究了死亡率选择在决定晚年死亡易感性变化中的作用,有人认为这是这种负相关的原因。我们证明,考虑到脆弱性异质性的固定脆弱性模型并不能消除这种相关性,而且这种相关性是冈珀茨分布的一种固有统计特性。将精算衰老率和生物学衰老率联系起来仍将是一个紧迫的挑战,但斯特勒 - 米尔德万相关性本身不应被用于诊断任何生物学、生理学或进化过程。这些发现解决了影响衰老和死亡率的进化与生物学研究的理论与数据之间的一些关键矛盾。衰老进化理论的检验应包括对生理性能或状况的直接测量。

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