E. Tandberg et al., Excessive daytime sleepiness and sleep benefit in Parkinson's disease: A community-based study, MOVEMENT D, 14(6), 1999, pp. 922-927
The objective of this study was to investigate the frequency of excessive d
aytime sleepiness (EDS) and the beneficial effect of sleep on motor perform
ance in an unselected community-based sample of patients with Parkinson's d
isease (PD). Furthermore, we wanted to identify possible risk factors to th
ese phenomena. Detailed information on somnolence and sleep during daytime,
as well as sleep benefit (SB) on awakening, was collected through a questi
onnaire among 245 patients with PD. Daytime somnolence was graded in groups
of no somnolence, mild daytime sleepiness, and EDS. In addition, the occur
rence of somnolence in the patients with PD was compared with the occurrenc
e among control groups of patients with diabetes mellitus and of healthy el
derly subjects. The correlations between EDS and SB and various motor- and
non-motor symptoms of PD were evaluated. Among the patients with PD, 15.5%
experienced EDS, significantly more than in the patients with diabetes mell
itus (4%) and the healthy control subjects (1%). The frequency of mild dayt
ime sleepiness was similar (10%) in patients with PD and control subjects.
The patients with EDS had significantly higher staging of PD, were more dis
abled, and showed a higher frequency of cognitive decline compared with the
patients without somnolence. They also had been using levodopa for a longe
r time and had more hallucinations. The occurrence of nocturnal sleeping pr
oblems and the use of sleeping pills was similar in the two groups, as was
the mean age at examination, duration of PD, and presence of fluctuations a
nd dyskinesias. SB was found in 42.2% of the patients with PD. These patien
ts had been using levodopa for significantly longer and had significantly m
ore fluctuations and dyskinesias compared with the patients without SB. Our
results suggest that mild daytime sleepiness may be a result of normal agi
ng, whereas more severe EDS can be explained by the neuropathologic changes
of PD. The data from this community-based study confirms the previously re
ported high frequencies of SB.