Table 1:
Recommendations for sleep and circadian research aimed at the prevention or treatment of Alzheimer Disease (AD)
No AD pathology | Preclinical (asymptomatic) AD | Symptomatic AD | |
---|---|---|---|
Basic research | Identify mechanisms linking sleep to Aβ/tau production/clearance | Examine effect of different sleep/circadian-promoting drugs or interventions on tau aggregation, inflammation, synaptic function, other degenerative processes in preclinical models. | |
| |||
Clinical research | Longitudinal (20 + years) followup studies | AD biomarker assessment regardless of cognitive status | Test effect of existing treatments on cognitive outcomes, with specific attention to safety & tolerability |
Objective measures of sleep and circadian function | Objective measures of sleep and circadian function | ||
Analytic methods for non-linear risk factors (e.g. sleep time) | Assess for obstructive sleep apnea and other sleep disorders | Identify and test new non-sedating therapies for sleep-circadian disruption in dementia patients | |
Assess for obstructive sleep apnea and other sleep disorders | Test effect of existing treatments (ex: PAP for OSA; medication for insomnia) on AD markers | ||
Genetic, race/ethnicity | Genetic, race/ethnicity | ||
Sleep-circadian biomarkers | |||
| |||
Trials and implementation | Screening measures for abnormal sleep/circadian function | ||
Tractable markers of abnormal sleep/circadian dysfunction | |||
Determination of a goal range. | |||
Education and outreach |