Abstract

Several organisms, including humans, display a deceleration in mortality rates at advanced ages. This mortality deceleration is sufficiently rapid to allow late-life mortality to plateau in old age in several species, causing the apparent cessation of biological ageing. Here, it is shown that late-life mortality deceleration (LLMD) and late-life plateaus are caused by common demographic errors. Age estimation and cohort blending errors introduced at rates below 1 in 10,000 are sufficient to cause LLMD and plateaus. In humans, observed error rates of birth and death registration predict the magnitude of LLMD. Correction for these sources of demographic error using a mixed linear model eliminates LLMD and late-life mortality plateaus (LLMPs) without recourse to biological or evolutionary models. These results suggest models developed to explain LLMD have been fitted to an error distribution, that ageing does not slow or stop during old age in humans, and that there is a finite limit to human longevity.

Highlights

  • The age-specific probability of death follows diverse, often species-specific curves

  • Mortality rates increase with age at a relatively fixed rate within populations

  • These findings suggest that human late-life mortality plateaus are largely, if not entirely, artefacts of error processes

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Summary

Introduction

The age-specific probability of death follows diverse, often species-specific curves. LLMD and late-life mortality plateaus (LLMPs) have been proposed to cause the respective slowing or cessation of biological ageing at advanced ages [2] and, respectively, increase and remove the upper limits of survival in humans [3,4] These findings have led to continuing debate on the biological meaning, magnitude, and importance of LLMDs and LLMPs. Several hypotheses and models have been proposed to explain the observation of LLMPs and LLMDs in diverse taxa, such as population heterogeneity, density effects, and evolutionary theories [5,6,7,8,9]. These observations have led to the development and widespread use [10] of demographic models, such as the Kannisto oldage–mortality model [11,12], that assume a priori the existence of LLMPs

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