Authors
Archibold Mposhi, Kerstin Uvnas-Moberg, Jonathan D Turner
Published in
Ageing research reviews. Pages 103343. Aug 29, 2026. Epub Aug 29, 2026.
Abstract
Non-communicable diseases (NCDs) dominate global mortality yet remain pervasive despite extensive prevention efforts, suggesting current explanatory frameworks may be incomplete. We propose the "Adaptive Cost Hypothesis": many NCDs represent not primarily lifestyle-mismatch diseases but rather inevitable trade-offs inherent in adaptive epigenetic programming optimized for reproductive success within ancestral human lifespans of 40-60 years. Early-life adversity calibrates immune, metabolic, and stress-response systems through epigenetic mechanisms. These adaptations enhance survival to reproduction that accumulate costs when lifespans extend to 70-90 years. This framework integrates evolutionary biology, developmental origins of health and disease (DOHaD), and transgenerational epigenetic inheritance, explaining the NCD epidemic as consequence of medical science extending life beyond our biology's evolutionary design parameters. Evidence from hunter-gatherers showing age-related pathology despite ancestral lifestyles, together with epigenetic clock data showing structured biological ageing even in health-optimised individuals, is inconsistent with mismatch alone and supports this perspective. Implications include prioritizing early-life prevention over midlife intervention, precision medicine based on epigenetic "immune biography" profiling, and redefining healthy aging as functional preservation despite inevitable pathology rather than disease elimination. Accepting NCDs as partially intrinsic to extended lifespan while pursuing interventions delaying onset may yield more realistic health goals than assuming complete preventability. Recent experimental work in murine infection models provides proof of concept that adaptive mechanisms can impose age-dependent costs at the molecular level consistent with the pleiotropic logic underpinning this framework.
PMID:
42668122
Bibliographic data and abstract were imported from PubMed on 30 Aug 2026.
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