October 5, 2026

A study investigates the relationship between substance use, including alcohol and opioids, and biological aging, revealing significant associations with epigenetic age acceleration.

This study explores how blood cell composition affects DNA methylation age and its association with health outcomes, revealing distinct biological interpretations.

This study explores a new DNA methylation clock model that predicts all-cause mortality using epigenetic data, highlighting immune-metabolic aging signatures.

This study explores the relationship between various substance uses, including alcohol and opioids, and biological aging, revealing significant associations with epigenetic age measures.

This study develops a DNA methylation clock that identifies immune-metabolic aging signatures associated with mortality, utilizing data from the Framingham Heart Study.

This study explores how blood cell composition impacts the interpretation of DNA methylation age and age acceleration, revealing distinct biological processes.

This study explores how neighborhood amenities, health services, and infrastructure affect epigenetic aging, suggesting local resources may slow biological aging.

A study explores a novel DNA methylation clock that predicts mortality based on immune-metabolic aging signatures, utilizing data from the Framingham Heart Study.

This study explores how blood cell composition affects DNA methylation age and its association with health outcomes, revealing distinct biological interpretations of age metrics.

This study investigates how neighborhood amenities, health services, and infrastructure influence epigenetic aging, suggesting a link between local resources and biological aging.