Older adults who experience a 3% slowdown in DunedinPACE, a biomarker of aging, through caloric restriction have a 15% lower risk of death compared to those who do not.
Mechanism
Synthesis from 1 study
Eating fewer calories changes how genes are regulated in cells, turning down inflammation and turning up repair processes. This slows the body's biological aging clock, which is linked to a lower chance of dying from age-related diseases.
Most probable mechanism
Eating fewer calories changes how genes are turned on and off in cells, especially those involved in repairing damage and controlling inflammation. This shifts the body into a slower aging mode, reducing the rate at which tissues and organs decline over time, which lowers the chance of death.
Reduced energy intake decreases activation of nutrient-sensing pathways including mTOR and increases activity of AMPK and sirtuins
Altered nutrient-sensing signaling modifies the activity of DNA methyltransferases and demethylases, leading to site-specific changes in DNA methylation patterns
These methylation changes suppress pro-inflammatory gene expression and enhance expression of genes involved in DNA repair, autophagy, and metabolic efficiency
The cumulative effect of these molecular shifts reduces the rate of physiological decline across multiple organ systems, as captured by the DunedinPACE epigenetic clock
A 3% slowing of DunedinPACE reflects a reduced pace of biological aging that correlates with lower incidence of age-related disease and mortality
Evidence from Studies
Supporting (1)
Community contributions welcome
EFFECT OF LONG-TERM CALORIC RESTRICTION ON THE PACE OF BIOLOGICAL AGING IN HEALTHY ADULTS FROM THE CALERIE TRIAL
Contradicting (0)
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Gold Standard Evidence Needed
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