In total, 208 participants were recruited, of which 107 did not participate in the study, as they were excluded based on inclusion criteria (see Methods), if sleep apnea were detected (>15/hour) or decided to withdraw. Participants underwent [18F]Flutemetamol (n = 96)/[18F]Florbetapir (n = 4) PET scan to assess Aβ burden, which we extracted over the earliest affected regions; they were also tested via an extensive battery of neuropsychological tasks from which we extracted global score, as well as performance over 3 main cognitive domains (attention, executive, and memory); and habitual sleep was recorded via EEG from which arousals were automatically detected.