Rhythmic movement disorder: polysomnographic study and summary of reported cases
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Published on: January 25, 2016
Jun Kohyama1, Fumie Matsukura, Kaku Kimura
1Human Ontogeny and Childhood Development, Graduate School, Tokyo Medical and Dental University, 1-5-45 Yushima, Tokyo 113-8519, Japan. jkohyama.ped@tmd.ac.jp
Insights
Rhythmic movement disorder (RMD) can occur during all sleep stages, including REM sleep. This suggests RMD may have multiple underlying causes, requiring further investigation into distinct patient subgroups.
Area of Science:
- Neurology
- Sleep Medicine
- Movement Disorders
Background:
- Rhythmic movement disorder (RMD) is typically classified as a sleep-wake transition disorder.
- However, RMD episodes have been observed during rapid-eye-movement (REM) sleep, a stage characterized by muscle atonia.
Observation:
- This study investigated RMD in two children using polysomnography.
- Rhythmic movements were observed across all sleep stages, including REM sleep, in both patients.
- Analysis of polysomnographic reports from 33 RMD patients revealed varied occurrences during REM sleep.
Findings:
- While RMD can occur during REM sleep, it is not exclusive to this stage.
- Some RMD patients experience episodes solely during REM sleep, while others do not.
- Normal REM sleep atonia indices and gross movement patterns were observed in the studied patients.
Implications:
- The findings suggest RMD may comprise distinct subgroups with different underlying neurobiological mechanisms.
- Further research is needed to differentiate these subgroups based on sleep stage involvement and underlying pathophysiology.
- This could lead to more targeted diagnostic and therapeutic approaches for RMD patients.
Abstract:
Rhythmic movement disorder (RMD) is classified as a sleep-wake transition disorder. However, some RMD patients show rhythmic movements during rapid-eye-movement (REM) sleep, during which muscle activity is completely absent. In order to determine the sleep stages in which episodes of RMD occur, we investigated two children with RMD by means of polysomnography, and also summarized the polysomnographic reports on patients with RMD. We also quantified the REM sleep atonia in our patients using the tonic and phasic inhibition indices (TII and PII). In addition, to examine the involvement of the basal ganglia in RMD patients, we studied the frequency of gross movements (GMs) during sleep in each sleep stage. Both patients showed rhythmic movements in all sleep stages, i.e. including REM sleep. Few rhythmic movements occurred during sleep-wake transition periods. Both patients showed normal TII and PII scores as well as a normal pattern for the sleep stage-dependent modulation of GMs during sleep. Eighteen of the 33 reported RMD patients, including ours, experienced episodes during REM sleep, while the other 15 patients had no episodes during REM sleep. Among the 18 patients who had episodes during REM sleep, eight experienced the episodes exclusively during REM sleep. It is unlikely that the neuronal mechanisms that underlie RMD episodes were the same in the 15 patients who had no RMD episodes during REM sleep and the eight who had them only during REM sleep. We propose that RMD can be divided into several subgroups according to the differences in the underlying neuronal mechanisms.
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