COIOS
Tomorrow's world Item refines peer-reviewed

Proteomic organ clocks tracked 16-year mortality slightly less than epigenetic age

In the Lothian Birth Cohort 1936, accelerated liver, immune and heart proteomic ages were associated with 16-year mortality at hazard ratios of 1.38-1.43 per standard deviation, against 1.44-1.62 for GrimAge2, brain volume, respiratory function and cognition.

The study benchmarked plasma proteomic organ clocks against established ageing biomarkers for association with 16-year all-cause mortality in 861 members of the Lothian Birth Cohort 1936, among whom 444 died. Liver, immune and heart organ clocks carried hazard ratios of 1.38-1.43 per standard deviation, while epigenetic age, total brain and grey matter volume, respiratory function and cognition ranged from 1.44 to 1.62. A separate survival analysis of 9703 protein targets identified 368 associated with mortality, led by GDF15 at 1.56 per standard deviation.

Why it is interesting: A head-to-head comparison in one cohort sets the newer proteomic organ clocks against older epigenetic and functional measures for predicting death.

Source
Aging Cell, 1 October 2026
DOI
10.1111/acel.70747
Type
Peer-reviewed article
Design
Prospective cohort, Lothian Birth Cohort 1936, 861 participants, 444 deaths over 16 years; Cox regression benchmarking of ageing biomarkers and 9703 plasma protein targets
Verdict
Refines prior evidence
Driver
Slowing ageing itself
Driver
Frailty and multimorbidity