Isolated rapid eye movement sleep without atonia in amyotrophic lateral sclerosis

- Only few cases with REM sleep behavior disorder (RBD) have been previously reported in amyotrophic lateral sclerosis (ALS).
- It is unknown if ALS per se impairs sleep motor function, besides respiration.
- Rapid eye movement (REM) sleep without atonia (RSWA) was found to be frequent in ALS patients without RBD.
- RSWA without RBD correlates with ALS severity.
- The mechanisms by which ALS pathology causes RSWA may be multiple and complex.

ObjectiveThe aim of this study was to quantitatively analyze, with the most recent and advanced tools, the presence of periodic leg movements during sleep (PLMS) and/or rapid eye movement (REM) sleep without atonia (RSWA), in a group of patients with amyotrophic lateral sclerosis (ALS), and to assess their eventual correlation with the clinical severity of the disease.MethodsTwenty-nine ALS patients were enrolled (mean age 63.6 years) along with 28 age-matched “normal” controls (mean age 63.8 years). Functional impairment due to ALS was evaluated using the ALS-Functional Rating Scale-Revised (ALS-FRS) and the ALS severity scale (ALSSS). Full video polysomnographic night recordings were obtained, and PLMS were analyzed by considering their number/hour of sleep and periodicity index, the distribution of intermovement intervals, and the distribution during the night. The characteristics of the chin electromyogram (EMG) amplitude during REM sleep were analyzed by means of the automatic atonia index and the number of chin EMG activations (movements).ResultsThe ALS patients showed longer sleep latency than the controls, together with an increase in number of stage shifts, increased sleep stage 1, and decreased sleep stage 2. None of the leg PLMS parameters were different between the ALS patients and controls. The REM atonia index was significantly decreased in the ALS patients, and the number of chin movements/hour tended to increase. Both REM atonia index and number of chin movements/hour correlated significantly with the ALS-FRS; REM atonia was higher and chin movements were less in ALS patients with more preserved function (higher scores on the ALS-FRS).ConclusionAbnormal REM sleep atonia seemed to be a genuine effect of ALS pathology per se and correlated with the clinical severity of the disease. It is unclear if this might constitute the basis of a possible risk for the development of REM sleep behavior disorder or represent a form of isolated RSWA in ALS.