학술논문

Mid-life epigenetic age, neuroimaging brain age, and cognitive function: coronary artery risk development in young adults (CARDIA) study
Document Type
article
Source
Aging. 14(4)
Subject
Dementia
Genetics
Clinical Research
Aging
Neurosciences
Neurodegenerative
Prevention
Brain Disorders
Behavioral and Social Science
Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)
Acquired Cognitive Impairment
Alzheimer's Disease
Underpinning research
Detection
screening and diagnosis
1.1 Normal biological development and functioning
4.1 Discovery and preclinical testing of markers and technologies
Neurological
Mental health
Good Health and Well Being
Biomarkers
Brain
Cognition
Cognitive Dysfunction
Cohort Studies
Coronary Vessels
Epigenesis
Genetic
Humans
Longitudinal Studies
Neuroimaging
cognitive function
epigenetic age
brain age
DNA methylation
magnetic resonance
magnetic resonance imaging
Biochemistry and Cell Biology
Physiology
Oncology and Carcinogenesis
Developmental Biology
Language
Abstract
The proportion of aging populations affected by dementia is increasing. There is an urgent need to identify biological aging markers in mid-life before symptoms of age-related dementia present for early intervention to delay the cognitive decline and the onset of dementia. In this cohort study involving 1,676 healthy participants (mean age 40) with up to 15 years of follow up, we evaluated the associations between cognitive function and two classes of novel biological aging markers: blood-based epigenetic aging and neuroimaging-based brain aging. Both accelerated epigenetic aging and brain aging were prospectively associated with worse cognitive outcomes. Specifically, every year faster epigenetic or brain aging was on average associated with 0.19-0.28 higher (worse) Stroop score, 0.04-0.05 lower (worse) RAVLT score, and 0.23-0.45 lower (worse) DSST (all false-discovery-rate-adjusted p