Diet, Pace of Biological Aging, and Risk of Dementia in the Framingham Heart Study

弗雷明翰心脏研究 痴呆 弗雷明翰风险评分 步伐 医学 老年学 内科学 疾病 地理 大地测量学
作者
Aline Thomas,Calen P. Ryan,Avshalom Caspi,Zhonghua Liu,Terrie E. Moffitt,Karen Sugden,Jiayi Zhou,Daniel W. Belsky,Yian Gu
出处
期刊:Annals of Neurology [Wiley]
卷期号:95 (6): 1069-1079 被引量:25
标识
DOI:10.1002/ana.26900
摘要

Objective People who eat healthier diets are less likely to develop dementia, but the biological mechanism of this protection is not well understood. We tested the hypothesis that healthy diet protects against dementia because it slows the pace of biological aging. Methods We analyzed Framingham Offspring Cohort data. We included participants ≥60 years‐old, free of dementia and having dietary, epigenetic, and follow‐up data. We assessed healthy diet as long‐term adherence to the Mediterranean‐Dash Intervention for Neurodegenerative Delay diet (MIND, over 4 visits spanning 1991–2008). We measured the pace of aging from blood DNA methylation data collected in 2005–2008 using the DunedinPACE epigenetic clock. Incident dementia and mortality were defined using study records compiled from 2005 to 2008 visit through 2018. Results Of n = 1,644 included participants (mean age 69.6, 54% female), n = 140 developed dementia and n = 471 died over 14 years of follow‐up. Greater MIND score was associated with slower DunedinPACE and reduced risks for dementia and mortality. Slower DunedinPACE was associated with reduced risks for dementia and mortality. In mediation analysis, slower DunedinPACE accounted for 27% of the diet‐dementia association and 57% of the diet‐mortality association. Interpretation Findings suggest that slower pace of aging mediates part of the relationship of healthy diet with reduced dementia risk. Monitoring pace of aging may inform dementia prevention. However, a large fraction of the diet‐dementia association remains unexplained and may reflect direct connections between diet and brain aging that do not overlap other organ systems. Investigation of brain‐specific mechanisms in well‐designed mediation studies is warranted. ANN NEUROL 2024;95:1069–1079
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