Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice
Abstract
Current concepts regarding the biology of aging are primarily based on studies aimed at identifying factors regulating lifespan. However, lifespan as a sole proxy measure for aging can be of limited value because it may be restricted by specific pathologies. Here, we employ large-scale phenotyping to analyze hundreds of markers in aging male C57BL/6J mice. For each phenotype, we establish lifetime profiles to determine when age-dependent change is first detectable relative to the young adult baseline. We examine key lifespan regulators (putative anti-aging interventions; PAAIs) for a possible countering of aging. Importantly, unlike most previous studies, we include in our study design young treated groups of animals, subjected to PAAIs prior to the onset of detectable age-dependent phenotypic change. Many PAAI effects influence phenotypes long before the onset of detectable age-dependent change, but, importantly, do not alter the rate of phenotypic change. Hence, these PAAIs have limited effects on aging.
From the paper
- Result
This was also supported by the slope of the regression line, which did not significantly differ from 1 (slope estimate: 0.91 ± 0.13; 95% CI: 0.65, 1.17; p = 0.491).
- Limitation
We did not use a longitudinal study design to infer aging trajectories and intervention effects.
Quoted word for word from the full text on PubMed Central.
The paper
German Center for Neurodegenerative Diseases
Nature Communications, 11 Nov 2022, Open access

