Protective effects of sleep duration and physical activity on cognitive performance are influenced by ß-amyloid and brain volume but not tau burden among cognitively unimpaired older adults.

BACKGROUND AND OBJECTIVES: Sleep and physical activity have gained traction as modifiable risk factors for Alzheimer's disease. Sleep duration is linked to amyloid-ß clearance while physical activity is associated with brain volume maintenance. We investigate how sleep duration and physical activity are associated with cognition by testing if the associations between sleep duration or physical activity to cognition are explained by amyloid-ß burden and brain volume, respectively. Additionally, we explore the mediating role of tau deposition in sleep duration-cognition and physical activity-cognition relationships. METHODS: This cross-sectional study obtained data from participants in the Anti-Amyloid Treatment in Asymptomatic Alzheimer's Disease (A4) study, a randomized clinical trial. In trial screening, cognitively unimpaired participants (age 65-85 years) underwent amyloid PET and brain MRI; APOE genotype and lifestyle questionnaire data were obtained. Cognitive performance was assessed using the Preclinical Alzheimer Cognitive Composite (PACC). Self-reported nightly sleep duration and weekly physical activity were the primary predictors. Regional Aß and tau pathologies and volumes were the proposed variables influencing relationships between sleep duration or physical activity and cognition. RESULTS: Aß data were obtained from 4322 participants (1208 with MRI, 59% female, 29% amyloid positive). Sleep duration was associated with a Aß composite score (ß = -0.005, CI: (-0.01, -0.001)) and Aß burden in the anterior cingulate (ACC) (ß = -0.012, CI: (-0.017, -0.006)) and medial orbitofrontal cortices (MOC) (ß = -0.009, CI: (-0.014, -0.005)). Composite (ß = -1.54, 95% CI:(-1.93, -1.15)), ACC (ß = -1.22, CI:(-1.54, -0.90)) and MOC (ß = -1.44, CI:(-1.86, -1.02)) Aß deposition was associated with PACC. Sleep duration-PACC association was explained by Aß burden in path analyses. Physical activity was associated with hippocampal (ß = 10.57, CI: (1.06, 20.08)), parahippocampal (ß = 9.3, CI: (1.69, 16.91)), entorhinal (ß = 14.68, CI: (1.75, 27.61), and fusiform gyral (ß = 38.38, CI: (5.57, 71.18)) volumes, which were positively associated with PACC (p < 0.02 for hippocampus, entorhinal cortex and fusiform gyrus). Physical activity-cognition relationship was explained by regional volumes. PET tau imaging was available for 443 participants. No direct sleep duration-tau burden, physical activity by tau burden, or mediation by regional tau was observed in sleep duration-cognition or physical activity-cognition relationships. DISCUSSION: Sleep duration and physical activity are associated with cognition through independent paths of brain Aß and brain volume, respectively. These findings implicate neural and pathological mechanisms for the relationships between sleep duration and physical activity on cognition. Dementia risk reduction approaches that emphasize the adequate sleep duration and a physically active lifestyle may benefit those with risk for Alzheimer's disease.