通过Gompertz-Makeham定律的概括来评估晚年人类死亡动力学的一个未被充分认识的特性。

IF 4.4 4区 医学 Q1 GERIATRICS & GERONTOLOGY Biogerontology Pub Date : 2024-06-01 Epub Date: 2023-11-25 DOI:10.1007/s10522-023-10079-2
A Golubev
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引用次数: 0

摘要

生物老年学非常重视在特定物种的寿命结束时,例如在人类大约90岁之后,死亡率随年龄增长的减速。根据Gompertz定律µ(t)=µ0e^γt及其固有的lnµon t依赖性的线性分析,通常认为这反映了种群的异质性,其中较弱的受试者死得早,从而增加了那些死亡较慢的人的比例,并导致人口老龄化率下降。利用1920年、1950年、1980年、2018年和2020年五个时期法国、瑞典和日本的人类死亡率数据库数据以及1920年出生的队列数据,对ln μ vs-t图进行黄土平滑处理并构造结果的一阶导数表明,生命表老龄化率(LAR)在晚年减速之前先有加速。它从65年开始,使85年左右的LAR比加速前高30%此后,LAR减小,约90年时达到加速前水平。这种特性不能用较弱的主体在较早年龄死亡来解释。其合理的解释可能是人类在65-70岁以上的年龄加速了生物衰老,这明显与退休相吻合。因此,减缓的生物衰老可能有助于随后的晚年LAR减速。根据广义Gompertz-Makeham定律µ(t) = C(t)+µ0e^f(t)讨论了这些发现的生物学意义。
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An underappreciated peculiarity of late-life human mortality kinetics assessed through the lens of a generalization of the Gompertz-Makeham law.

Much attention in biogerontology is paid to the deceleration of mortality rate increase with age by the end of a species-specific lifespan, e.g. after ca. 90 years in humans. Being analyzed based on the Gompertz law µ(t)=µ0e^γt with its inbuilt linearity of the dependency of lnµ on t, this is commonly assumed to reflect the heterogeneity of populations where the frailer subjects die out earlier thus increasing the proportions of those whose dying out is slower and leading to decreases in the demographic rates of aging. Using Human Mortality Database data related to France, Sweden and Japan in five periods 1920, 1950, 1980, 2018 and 2020 and to the cohorts born in 1920, it is shown by LOESS smoothing of the lnµ-vs-t plots and constructing the first derivatives of the results that the late-life deceleration of the life-table aging rate (LAR) is preceded by an acceleration. It starts at about 65 years and makes LAR at about 85 years to become 30% higher than it was before the acceleration. Thereafter, LAR decreases and reaches the pre-acceleration level at ca. 90 years. This peculiarity cannot be explained by the predominant dying out of frailer subjects at earlier ages. Its plausible explanation may be the acceleration of the biological aging in humans at ages above 65-70 years, which conspicuously coincide with retirement. The decelerated biological aging may therefore contribute to the subsequent late-life LAR deceleration. The biological implications of these findings are discussed in terms of a generalized Gompertz-Makeham law µ(t) = C(t)+µ0e^f(t).

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来源期刊
Biogerontology
Biogerontology 医学-老年医学
CiteScore
8.00
自引率
4.40%
发文量
54
审稿时长
>12 weeks
期刊介绍: The journal Biogerontology offers a platform for research which aims primarily at achieving healthy old age accompanied by improved longevity. The focus is on efforts to understand, prevent, cure or minimize age-related impairments. Biogerontology provides a peer-reviewed forum for publishing original research data, new ideas and discussions on modulating the aging process by physical, chemical and biological means, including transgenic and knockout organisms; cell culture systems to develop new approaches and health care products for maintaining or recovering the lost biochemical functions; immunology, autoimmunity and infection in aging; vertebrates, invertebrates, micro-organisms and plants for experimental studies on genetic determinants of aging and longevity; biodemography and theoretical models linking aging and survival kinetics.
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