VII. Supplementary
Questions and answers from the Supporting Information of the PNAS article.
- 1.What is time in aging?
- 2.Which disciplines converge to explain aging?
- 3.How random is the deleteriome?
- 4.Can future aging states be reliably predicted?
- 5.Is there a space of possible aging, and where do existing species sit within it?
- 6.Why does aging impose an arrow of time inside organisms?
- 7.Do bacteria age?
- 8.What are hallmarks of aging?
- 9.What is intrinsic capacity, and why does it matter for aging?
- 10.What is negligible senescence?
- 11.What does evolution select with regard to aging?
- 12.Does antigeria represent decelerated aging?
- 13.Why does life require rejuvenation across generations?
- 14.Is cellular senescence a cause of aging?
- 15.Is chronic inflammation a cause of aging?
- 16.Is oxidative damage a cause of aging?
- 17.Do telomeres drive aging?
- 18.Does mitochondrial dysfunction drive aging?
- 19.Are epigenetic changes causes of aging or readouts?
- 20.Is ‘aging begins at gastrulation’ literal?
- 21.What have we learned from aging of model organisms as applied to humans?
- 22.What is the relationship between programmed cell death and aging?
- 23.Why does lifespan often vary across sexes?
- 24.Is there evidence for adult age reversal in biomarkers?
- 25.Why do epigenetic clocks generalize so well?
- 26.What is systems aging?
- 27.What does validation mean for an aging biomarker?
- 28.What are longevity intervention types?
- 29.How do within-species lifespan interventions differ from cross-species longevity differences?
- 30.Why do many interventions have modest effects in mammals?
- 31.Why do interventions work across species?
- 32.Why can organ-specific strategies be more beneficial than universal interventions?
- 33.What is the evidence that aging is modifiable in mammals?
- 34.What are the conserved pathways that modulate aging?
- 35.What makes an intervention translationally credible for humans?
- 36.Can pharmacology slow aging?
- 37.Can an intervention extend lifespan without slowing the underlying rate of aging?
- 38.How does hormesis work and can it slow aging?
- 39.Can temperature modulation slow aging?
- 40.Where does sleep fit in aging biology?
- 41.Why does exercise help even though it is a stress?
- 42.Why do universal longevity interventions often involve tradeoffs?
- 43.What are realistic near-term goals in aging biology?
- 44.Can aging be stabilized?
- 45.If we rejuvenate an organ, would it change the biological age of the organism?
- 46.What are the main risks of rejuvenation therapies?
- 47.Why might combination therapies be necessary?
- 48.Are senolytics a form of rejuvenation?
- 49.What are major recent advances in the field?
- 50.Would progress come from individual labs or large, collaborative efforts?
- 51.How can aging research impact public health in the future?
- 52.Which funding or regulatory policy changes could speed up progress?
- 53.What can researchers do to ensure that aging science can be trusted?
- 54.What advice may be given to researchers entering the field now?
- 55.Where will the field be in the next 5 to 10 years?
- 56.Is cryonics a viable strategy for longevity?
- 57.Can damage dilution be engineered?
- 58.How should we implement slowing aging and rejuvenation?