No evidence for squaring the survival curve: lifespan-extending treatments increase variation in age- at-death

Geroscience has the goal of extending lifespan through geroprotective interventions. These interventions are typically imparted on groups of individuals, with their efficacy judged by increases in the average age-at-death. A more equitable outcome, which looks beyond the average, is to attain a long life for all individuals, such that the average age-at-death is high while variability (e.g. standard deviation in age-at-death) is low. This goal of increasing the mean while reducing variation is sometimes referred to as 'squaring the survival curve'. A recent meta-analysis of vertebrate data found that dietary restriction (DR) and the DR-mimetic, rapamycin, generally increase the average age-at-death, while metformin (also considered a DR-mimetic) is less effective. We have re-analysed this recently published data to study the effects of lifespan-extending treatments on variation in the age-at-death. On average, all three treatments increase the variance in the age-at-death, but not the coefficient of variation (i.e. standard deviation relative to the mean). This suggests that lifespan-extending treatments do not reduce variance and 'square the survival curve'. Rather, any gains in mean age-at-death are matched by corresponding increases in variation. Interestingly, this result is consistent with the treatments proportionally reducing both the age-dependent and age-independent parameters in a Gompertz model of mortality.

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Publication Details

Journal
Biology Letters
Published
2026-02-25
DOI
https://doi.org/10.1098/rsbl.2025.0651
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
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article

No evidence for squaring the survival curve: lifespan-extending treatments increase variation in age- at-death

Tahlia L. Fulton, Erin L. Macartney, Alistair M. Senior
Biology Letters
Genetics, Aging, and Longevity in Model Organisms
article

No evidence for squaring the survival curve: lifespan-extending treatments increase variation in age- at-death

Tahlia L. Fulton, Erin L. Macartney, Alistair M. Senior
article en

Abstract

Geroscience has the goal of extending lifespan through geroprotective interventions. These interventions are typically imparted on groups of individuals, with their efficacy judged by increases in the average age-at-death. A more equitable outcome, which looks beyond the average, is to attain a long life for all individuals, such that the average age-at-death is high while variability (e.g. standard deviation in age-at-death) is low. This goal of increasing the mean while reducing variation is sometimes referred to as 'squaring the survival curve'. A recent meta-analysis of vertebrate data found that dietary restriction (DR) and the DR-mimetic, rapamycin, generally increase the average age-at-death, while metformin (also considered a DR-mimetic) is less effective. We have re-analysed this recently published data to study the effects of lifespan-extending treatments on variation in the age-at-death. On average, all three treatments increase the variance in the age-at-death, but not the coefficient of variation (i.e. standard deviation relative to the mean). This suggests that lifespan-extending treatments do not reduce variance and 'square the survival curve'. Rather, any gains in mean age-at-death are matched by corresponding increases in variation. Interestingly, this result is consistent with the treatments proportionally reducing both the age-dependent and age-independent parameters in a Gompertz model of mortality.

Biology LettersVol. 22(2)
The University of Sydney (AU), Johannes Gutenberg University Mainz (DE), UNSW Sydney (AU), University Medical Center of the Johannes Gutenberg University Mainz (DE)
Openalex Percentile: Top 40%
Genetics, Aging, and Longevity in Model Organisms
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