作者
M. Elliott,Avshalom Caspi,Renate Houts,Antony Ambler,Jonathan M. Broadbent,Robert J. Hancox,HonaLee Harrington,Sean Hogan,Rāwiri Keenan,Annchen R. Knodt,Joan H. Leung,Tracy R. Melzer,Suzanne C. Purdy,Sandhya Ramrakha,Leah S. Richmond‐Rakerd,Antoinette Righarts,Karen Sugden,W. Murray Thomson,Peter R. Thorne,Benjamin Williams,Graham Wilson,Ahmad R. Hariri,Richie Poulton,Terrie E. Moffitt
摘要
Some humans age faster than others. Variation in biological aging can be measured in midlife, but the implications of this variation are poorly understood. We tested associations between midlife biological aging and indicators of future frailty risk in the Dunedin cohort of 1,037 infants born the same year and followed to age 45. Participants’ ‘Pace of Aging’ was quantified by tracking declining function in 19 biomarkers indexing the cardiovascular, metabolic, renal, immune, dental and pulmonary systems across ages 26, 32, 38 and 45 years. At age 45 in 2019, participants with faster Pace of Aging had more cognitive difficulties, signs of advanced brain aging, diminished sensory–motor functions, older appearances and more pessimistic perceptions of aging. People who are aging more rapidly than same-age peers in midlife may prematurely need supports to sustain independence that are usually reserved for older adults. Chronological age does not adequately identify need for such supports. A cohort study tracking 20-year age-related declines in multiple organ systems finds that, already by midlife, those aging fastest showed cognitive declines, signs of brain aging, diminished sensory–motor function and negative views about aging.