Department of Mathematical Sciences, University of Liverpool, Liverpool, UK.
Exp Gerontol. 2013 Aug;48(8):801-11. doi: 10.1016/j.exger.2013.05.054. Epub 2013 May 23.
The mortality patterns in human populations reflect biological, social and medical factors affecting our lives, and mathematical modelling is an important tool for the analysis of these patterns. It is known that the mortality rate in all human populations increases with age after sexual maturity. This increase is predominantly exponential and satisfies the Gompertz equation. Although the exponential growth of mortality rates is observed over a wide range of ages, it excludes early- and late-life intervals. In this work we accept the fact that the mortality rate is an exponential function of age and analyse possible mechanisms underlying the deviations from the exponential law across the human lifespan. We consider the effect of heterogeneity as well as stochastic factors in altering the exponential law and compare our results to publicly available age-dependent mortality data for Swedish and US populations. In a model of heterogeneous populations we study how differences in parameters of the Gompertz equation describing different subpopulations account for mortality dynamics at different ages. Particularly, we show that the mortality data on Swedish populations can be reproduced fairly well by a model comprising four subpopulations. We then analyse the influence of stochastic effects on the mortality dynamics to show that they play a role only at early and late ages, when only a few individuals contribute to mortality. We conclude that the deviations from exponential law at young ages can be explained by heterogeneity, namely by the presence of a subpopulation with high initial mortality rate presumably due to congenital defects, while those for old ages can be viewed as fluctuations and explained by stochastic effects.
人口死亡率模式反映了影响我们生活的生物、社会和医学因素,数学建模是分析这些模式的重要工具。众所周知,在性成熟后,所有人类群体的死亡率都会随着年龄的增长而增加。这种增长主要是指数型的,并符合戈珀兹方程。尽管死亡率在广泛的年龄范围内呈指数增长,但它排除了生命早期和晚期的间隔。在这项工作中,我们接受死亡率是年龄的指数函数这一事实,并分析了人类寿命范围内偏离指数定律的可能机制。我们考虑了异质性和随机因素对指数定律的影响,并将我们的结果与瑞典和美国人口的公开可用的年龄相关死亡率数据进行了比较。在异质人群模型中,我们研究了描述不同亚群的戈珀兹方程的参数差异如何解释不同年龄的死亡率动态。特别是,我们表明,描述四个亚群的戈珀兹方程的参数差异可以很好地再现瑞典人口的死亡率数据。然后,我们分析了随机效应对死亡率动态的影响,以表明它们仅在早期和晚期起作用,那时只有少数个体对死亡率有贡献。我们得出结论,年轻时偏离指数定律可以用异质性来解释,即由于先天缺陷导致初始死亡率高的亚群的存在,而对于老年来说,这些可以看作是波动,可以用随机效应来解释。