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人类种特异性寿命和计算寿命老化率的趋势。

Trends in Human Species-Specific Lifespan and Actuarial Aging Rate.

机构信息

Academic Research Centers, NORC at the University of Chicago, 60637 Chicago, IL, USA.

Institute for Demographic Research, Federal Center of Theoretical and Applied Sociology, Russian Academy of Sciences, Moscow, 109028, Russia.

出版信息

Biochemistry (Mosc). 2022 Dec;87(12):1622-1633. doi: 10.1134/S0006297922120173.

Abstract

The compensation effect of mortality (CEM) was tested and species-specific lifespan was estimated using data on one-year age-specific death rates from the Human Mortality Database (HMD). CEM was confirmed using this source of the data and human species-specific lifespan estimates were obtained, which were similar to the estimates published before. Three models (Gompertz-Makeham, Gompertz-Makeham with mean-centered age, and Gompertz) produced similar estimates of the species-specific lifespan. These estimates demonstrated some increase over time. Attempts to measure aging rates through the Gompertz slope parameter led to the conclusion that actuarial aging rates were stable during most of the 20th century, but recently demonstrated an increase over time in the majority (74%) of studied populations. This recent phenomenon is most likely caused by more rapid historical decline of mortality at the younger adult age groups compared to the older age groups, thus making the age gradient in mortality steeper over time. There is no biomedical reason to believe that human aging rates accelerated recently, so that the actuarial aging rate is probably not a good measure of true aging rate (rate of functional loss). Therefore, better measures of aging rate need to be developed.

摘要

利用人类死亡率数据库(HMD)中关于一岁特定死亡率的数据,测试了死亡率补偿效应(CEM)并估计了物种特异性寿命。通过该数据源确认了 CEM,并获得了人类物种特异性寿命估计值,这些估计值与之前公布的估计值相似。三种模型(Gompertz-Makeham、以均值中心化年龄的 Gompertz-Makeham 和 Gompertz)对物种特异性寿命产生了相似的估计。这些估计值显示出随着时间的推移略有增加。通过 Gompertz 斜率参数测量衰老率的尝试得出的结论是,在 20 世纪的大部分时间里,精算衰老率是稳定的,但最近在大多数(74%)研究人群中,随着时间的推移呈现出增加的趋势。这种最近的现象很可能是由于与老年人群相比,年轻成年人群的死亡率在历史上更快地下降,从而导致死亡率的年龄梯度随着时间的推移变得更加陡峭。没有生物医学理由相信人类衰老率最近有所加快,因此,精算衰老率可能不是衡量真正衰老率(功能丧失率)的好指标。因此,需要开发更好的衰老率衡量指标。

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