A high-density electroencephalography study reveals abnormal sleep homeostasis in patients with rapid eye movement sleep behavior disorder

Rapid eye movement (REM) sleep behavior disorder (RBD) is characterized by disrupting motor enactments during REM sleep, but also cognitive impairments across several domains. In addition to REM sleep abnormalities, we hypothesized that RBD patients may also display EEG abnormalities during NREM sleep. We collected all-night recordings with 256-channel high-density EEG in nine RBD patients, predominantly early-onset medicated individuals, nine sex- and age- matched healthy controls, and nine additional controls with matched medications and comorbidities. Power spectra in delta to gamma frequency bands were compared during both REM and NREM sleep, between phasic and tonic REM sleep, and between the first versus last cycle of NREM sleep. Controls, but not RBD patients, displayed a decrease in beta power during phasic compared to tonic REM sleep. Compared to controls, RBD patients displayed a reduced decline in SWA from early to late NREM sleep. Overnight changes in the distribution of the amplitude of slow waves were also reduced in RBD patients. Without suppression of beta rhythms during phasic REM sleep, RBD patients might demonstrate heightened cortical arousal, favoring the emergence of behavioral episodes. A blunted difference between REM sleep sub-stages may constitute a sensitive biomarker for RBD. Moreover, reduced overnight decline in SWA suggests a reduced capacity for synaptic plasticity in RBD patients, which may favor progression towards neurodegenerative diseases.

. Epochs of steady stage of NREM stage 2 and 3 (N2 and N3) sleep and REM sleep were extracted. From the REM epochs, tonic and phasic segments were manually defined by visual inspection for the presence of rapid eye movements (with ocular quiescence for 3 s defining tonic REM sleep). NREM sleep cycles were defined according to the modified criteria of Feinberg and Floyd 52,53 . To increase signal-tonoise ratio, analyses were then restricted to 173 channels overlaying the scalp, excluding channels from the face and the neck (channels falling within a plotting radius of 0.57 from the center of the head specified in the topoplot function of EEGLAB). For REM sleep epochs, periods contaminated by artifacts were manually identified and rejected. For NREM sleep epochs, semi-automatic artifact rejection procedures were used to remove channels and epochs with high frequency noise, as previously done in [54][55][56] . Specifically, thresholds were automatically calculated for low (1)(2)(3)(4) and high  frequency ranges at the 99th percentile for each channel. Spectral power in these ranges across all 6-s NREM epochs for each channel was plotted, visually inspected and used to remove epochs. For both NREM sleep and REM sleep, channels with artifacts affecting a majority of the recording were removed. Additional spectral-based and topographic procedures were used to remove individual channels with distinctly greater power relative to neighboring channels. Overall, less than 25% of the channels were removed and subsequently interpolated using spherical interpolation. As in previous studies, independent component analysis (ICA) implemented in the EEGLAB toolbox (runica algorithm) was then applied to remove physiological noise such as Table 1. Medical details of the participants. The duration of illness for RBD patients began when symptoms were first noticed. The frequency of episodes ranged from a few times per week to a few times per month. One participant on clonazepam was not having episodes at the time of their study. n/a indicates that the frequency could not be precisely determined because of an absence of a bed partner or because of a vague medical description (such as "chronically acts out dreams"). *Indicates that clonazepam was tapered before the sleep study. The list of indicated medication includes any antidepressants, benzodiazepines, anticonvulsants or other CNS drugs, and excludes opioids, anti-hypertensives, corticosteroids, asthma medication or hormones. 5 HTP, serotonin; BP, bipolar disorder; GAD, general anxiety disorder; MDD, major depressive disorder. The medicated control group and RBD patients were not statistically different with regard to the occurrence of GAD, MDD, and the use of antidepressants, benzodiazepines, anticonvulsants and non-benzodiazepine hypnotics (Fisher's exact tests: all p > 0.05). Non medicated controls   44  F  ----46  F  ----61  F  ----34  M  ----40  M  ----48  M  ---- Slow wave detection. Preprocessed EEG data were re-referenced to linked mastoids for a finer analysis of slowwave characteristics. An automated detection algorithm based on zero crossings was used to identify individual slow waves 47,57 . Specifically, a negative-going signal envelope was calculated by selecting the fifth most negative sample across all selected channels (191 electrodes defined with a radius of 0.65 from the center of the head). Slow waves were defined as waves with frequency 0.5-2 Hz and no amplitude threshold. Slow-wave mean negative amplitude (μV) and negative slope (from the first zero-crossing to the negative peak) were estimated.

Group Age (years) Sex Medication Psychiatric disorders Duration of RBD illness (years) Frequency of RBD episodes
Statistical analyses. Between-group differences in demographic and polysomnographic variables (as shown in Table 2) were evaluated with one-way ANOVA followed by unpaired t-tests. Differences in PSDs between REM sleep sub-stages were tested with paired t-tests followed by false-discovery rate (FDR) correction. Differences in PSDs between the three groups during all-night REM and NREM sleep were tested using one-way ANOVA followed by FDR correction. Absolute power in scalp topographies were compared between groups using unpaired 2-tailed t-tests (such as in Supplementary Figs. 1 and 2). Paired t-tests were performed on absolute power topographies between states (phasic vs tonic REM in Fig. 1, early vs late NREM in Fig. 2). Absolute power in defined scalp regions (frontal and central clusters, consisting of 7 and 6 electrodes centered around Fz and Cz respectively) were compared in Region of Interest (ROI) analyses, with comparison between groups and states. Repeated-measure ANOVAs with "group" and "state" on absolute ROI powers were performed. Normalized power differences between states (first versus last NREM sleep cycle, phasic versus tonic REM sleep sub-stages) were calculated as the difference in power log values normalized by the power log value in the reference state (first NREM cycle and tonic REM sleep, respectively). To quantify differences between groups, we performed unpaired 2-tailed t-tests on these normalized power changes between states (inserts on the right in Figs. 1B, 2B). To identify significant clusters of electrodes, we used statistical nonparametric mapping with supra-threshold cluster tests to correct for multiple comparisons 58 with a cluster-forming threshold of t = 2.12, corresponding to an uncorrected α level of p < 0.05. In brief, topographic power maps are randomly shuffled between groups in all possible combinations (n = 48,620). The size of the largest cluster above the threshold for each reshuffling is then used to create a maximal cluster  White dots indicate p < 0.05 and black dots p < 0.1 after SNPM correction for one-sample t-test between both REM sleep sub-stages. Statistics on the changes showed significant differences between groups in the beta range only and are shown in the right insert. Individual channel t-maps are represented, with white dots indicating channels with SNPM corrected p < 0.05 and black dots uncorrected p < 0.05 after unpaired t-tests on the phasic to tonic REM power difference. (C) ROI analysis for central and frontal changes in absolute beta power between tonic and phasic REM sleep. Central and frontal ROIs were centered around Fz and Cz respectively and consisted of six and seven electrodes each (see inserts). Repeated-measure ANOVA with "group" and "REM sub-stage" on the log power revealed for the central cluster: a significant effect of REM sub-stage only (p < 0.01); for the frontal cluster: a significant effect of REM sub-stage (p < 0.01) and a trend for an interaction "group" × "REM sub-stage" (p = 0.056). * and ** for p < 0.05 and p < 0.01 Tukey Kramer post-hoc test between "tonic" and "phasic".  in non-medicated controls (left), medicated controls (middle) and patients (right). Left columns: White dots indicate p < 0.05 and black dots p < 0.1 after SNPM correction for one sample t-test on the change. Statistics on the changes showed significant differences between groups in the delta and theta range only and are shown in the right insert. Individual channel t-maps are represented, with white dots indicating channels with SNPM corrected p < 0.05 and black dots uncorrected p < 0.05 after unpaired t-tests on the late to early NREM power difference. (C) ROI analysis for change in frontal absolute delta power/SWA between early and late night. Frontal ROI was centered around Fz and consisted of seven electrodes (see insert). The expected decrease in absolute delta power/SWA is visible in both control groups but not in patients. Repeated-measure ANOVA with "group" and "time" revealed a significant interaction (p = 0.012). *** p < 0.001 Tukey Kramer post-hoc test between "early" and "late". The frontal delta power during the first cycle in RBD patients appeared lower compared to medicated controls at a trend level (p = 0.06). www.nature.com/scientificreports/ size distribution. The suprathreshold cluster P value is then determined by comparison of the actual cluster size against the maximal cluster size distribution. This cluster-based method takes into account the relevant information provided by neighboring electrodes. Changes in the distribution of slow-wave amplitude and slope from the first to the last NREM sleep cycle were assessed using repeated-measure ANOVA with factors "time" (early-late) and "group" (RBD, NMC, MC), followed by Bonferroni-corrected post-hoc tests. For all analyses, results were considered statistically significant at p-values < 0.05 corrected for multiple comparisons.

Results
Sleep architecture. Sleep parameters derived from the hdPSG recordings are summarized in Table 2. RBD patients did not differ significantly from both medicated and non-medicated controls in terms of sleep duration, sleep efficiency or sleep disorder indices (AHI, apnea-hypopnea index; AI, arousal index; PLMI, periodic leg movement index). Each group had similar amount of phasic and tonic REM sleep (22 ± 11% phasic REM). Relative to NMC, RBD patients and MC had increased time spent in N1 sleep and decreased time spent in N3 sleep (% N1: p = 0.017, 8.2 to 12.8% in MC and RBD vs 4.5% in NMC, % N3: p = 0.043, 4.8 to 8.6% in MC and RBD vs 14.9% in NMC). One participant in the medicated control group did not have enough clean phasic REM (< 3 min) to be included in the analyses.

REM sleep abnormalities.
In order to examine how RBD affected EEG power during REM sleep, we first looked at power spectral densities during REM sleep averaged over the whole night. We found no differences between groups (Supplementary Fig. 1A). There were also no group differences in the topographical scalp maps in any frequency bands ( Supplementary Fig. 1B).
To perform a more detailed analysis of REM sleep sub-stages, we then separated tonic vs phasic REM sleep. In both control groups, PSDs revealed an increased absolute power in the delta range and a decreased power in the beta range in phasic compared to tonic REM sleep (Fig. 1A). However, no significant differences between phasic and tonic REM sleep were found in the RBD patient group (Fig. 1A).
Scalp topographies of the power changes between phasic and tonic REM sleep confirmed the presence of a difference between RBD patients and controls. An increased delta power in fronto-central regions in phasic compared to tonic REM sleep was observed in both control groups as well as in RBD patients (Fig. 1B). However, while both control groups displayed a global reduction in beta power in phasic compared to tonic REM sleep, this decrease was limited to midline parietal regions in RBD patients (Fig. 1B). A post-hoc ROI analysis indeed illustrates that absolute beta power decreases from phasic to tonic REM in all groups in a central cluster of electrodes (ANOVA "sub-stage" p < 0.01) (Fig. 1C left). Statistical T-maps on the beta power change (Fig. 1B, right insert) confirmed that while all groups reported a decline of beta power in central regions, the beta power change in frontal regions was different in RBD patients compared to both control groups (50-54 electrodes with corrected p < 0.05 represented as white dots). A ROI analysis conducted in a frontal cluster confirmed a decrease in beta power in phasic REM sleep in both control groups (Fig. 1C right), but not in the RBD patient group (ANOVA "group x sub-stage" p = 0.056).

NREM sleep abnormalities.
We first checked for EEG spectral abnormalities in RBD patients during NREM sleep averaged across the whole night. Inspection of PSDs revealed no differences between groups (Supplementary Fig. 2A). With respect to the topographical maps ( Supplementary Fig. 2B), RBD patients displayed lower theta power over bilateral central regions compared to NMC. However, this effect was not replicated when comparing them to MC (which were themselves not significantly different from NMC).
To quantify sleep homeostasis, we compared EEG spectral activity during NREM sleep from the early part of the night (first cycle) and last part of the night (last cycle). In both control groups, delta and theta power reduced significantly from the early to the late part of NREM sleep ( Fig. 2A,B). In RBD patients, there was no significant decline in delta or theta power from the first to last part of NREM sleep ( Fig. 2A,B). Direct comparison between groups (Fig. 2B, right insert), revealed that patients demonstrated significantly less delta and theta power reduction over the course of the night in the left fronto-central and parietal regions as compared to both control groups.
Since frontal SWA is known to show the most reliable sleep homeostasis EEG effects at the between-subject level 59,60 , we also performed a post-hoc ROI analysis of SWA changes from early to late NREM cycle (Fig. 2C) within a frontal cluster of electrodes. We confirmed that, on average, frontal SWA significantly declined in both control groups, but not within the RBD patient group (repeated measure ANOVA "group" × "time" p = 0.012, post-hoc effect of time p < 0.001 in NMC and MC). This seemed to be mostly driven by lower SWA at the beginning of the night in RBD patients: there was a trend towards lower frontal SWA in patients compared to controls during the first cycle (post-hoc between-group comparison: p = 0.06 for RBD versus MC and p > 0.1 for RBD versus NMC), while mean SWA was similar in patients and controls at the end of the night (Fig. 2C).
We also performed a detailed analysis of slow-wave characteristics. There was no significant effect of group on mean slow wave amplitude or slope changes from early to late sleep (Supplementary Table 1). However, when we analyzed the distribution of amplitude of slow wave between the beginning and end of the night, we again observed an abnormal pattern in RBD patients compared to controls. In both control groups, as expected 47 , slow waves with higher amplitude were more frequent during early sleep, and conversely, slow waves with lower amplitude were more frequent during later sleep (Fig. 3). In RBD patients, this shift was less pronounced, with decreased occurrence of low-amplitude, shallow slow waves during the second part of the night, especially for smaller waves in the 10-20 µV slow wave amplitude range (ANOVA p < 0.05 "group" × "time" interaction).

Discussion
The present 256 electrode hdEEG study comparing nine RBD patients to two different control groups revealed consistent abnormalities in both REM sleep and NREM sleep. The decreased attenuation of beta frequency EEG activity during phasic compared to tonic REM sleep in RBD patients may reflect higher cortical arousal during phasic REM sleep, which may favor motor enactements. In addition, the reduced overnight decline in SWA observed in RBD patients during NREM sleep suggests a reduced capacity for neural plasticity in RBD patients, which may account for cognitive deficits and their predisposition to progress towards neurodegenerative diseases.

REM sleep abnormalities.
Our results indicate that contrasting brain activity during sub-stages of REM sleep may be helpful to understand the physiopathology of RBD. Indeed, no significant difference was found between RBD patients and controls when looking at overall REM sleep. These results are in line with the variable results found in the literature with two previous studies using standard low density PSG-EEG finding decreased beta power during REM sleep in RBD patients 61,62 , while others reported increases 63 or no changes 27,64 . In contrast, our main REM sleep finding is that RBD patients showed a loss of differentiation in brain activity between phasic and tonic REM sleep. These results suggest that differences between phasic and tonic REM sleep may be a more sensitive diagnostic marker to detect RBD. To note, our finding of a loss of differentiation between REM sub-stages in RBD patients is limited to the beta band (15)(16)(17)(18)(19)(20). This result should be interpreted with caution as this band has previously been shown to be affected by clonazepam, a medication taken by 4 of our 9 patients at the time of recording 64 . However, our analysis is controlled since we compared values within individuals between their two REM sub-stages and we showed no statistical differences between groups in absolute beta power in specific frontal and central regions. In addition, the chronic use of benzodiazepines is known to lead to less prominent sleep EEG changes 65 .
In healthy humans, phasic REM has been shown to be physiologically different from tonic REM sleep in several aspects. First, dreaming preferentially occurs in phasic REM periods [19][20][21] . In a human PET study, phasic REM was associated to primary occipital cortex activation (a region associated with visual mental imagery), while auditory evoked-related potentials 14 and fMRI responses 11 were suppressed in this sub-stage. In fact, the acoustic arousal threshold is higher in phasic REM sleep compared to tonic REM sleep 13 , and is overall highest compared to any other sleep stage. Previous studies also demonstrated a suppression of long-range inter-and intra-hemispheric EEG synchronization 15 , increased delta-theta activity 17,18 , increased gamma activity and decreased high alpha-beta activity in sensorimotor and higher order associative cortices 10,17,18,22 . With both our control groups, we here confirm the increase in delta/theta activity and attenuation of beta activity in phasic REM sleep. Our group recently showed that beta activity diffusely decreases during REM sleep compared to wake 66 , consistent with a decrease in cortical arousal. The dampened decrease in beta activity during phasic compared to tonic REM sleep in RBD patients suggests a reduction of the normal arousal suppression that protects active dreaming states. A central strength of our study is the use of high-density EEG-to our knowledge for the first time in patients with RBD-which allowed for a precise analysis of regional distribution of neural activity, suggesting that the abnormal regulation of REM sleep substages was most prominent within frontal cortices. Because frontal cortices are involved in motor behaviors, increased arousal in these regions during phasic REM sleep may predispose RBD patients to 'act out their dreams' . Our results may at first appear to contrast with a study that found a larger suppression of beta activity in phasic REM sleep of RBD patients 27 . However, one should be cautious about the interpretation of the results. Sunwoo et al. had a moderate spatial resolution of 21 electrodes limiting the accurate separation of eye movements from brain signals using ICA, in contrast to our dense electrode array of 173 electrodes. In addition, their samples consisted of only 90 s of selected REM sleep period, in comparison with our use of the totality of non-artefactual REM sleep from the nocturnal recordings. Taken together, the characterization of EEG activity during tonic and phasic REM sleep in RBD patients warrants further investigation. NREM sleep abnormalities. RBD patients displayed a blunted overnight decrease in delta and theta power during NREM sleep, including a blunted decrease in slow-wave amplitude compared to both control groups. This dampened overnight decline seemed to be related to decreased frontal delta power at the beginning Figure 3. Distribution of the amplitude of slow waves during early and late NREM sleep. Proportion of slow waves in each amplitude range in early (first cycle, horizontal striped bars) and late sleep (last cycle, filled bars), in each group. Repeated-measure ANOVA with factors "time" (early-late) and "group" (RBD, NMC, MC) were performed for each amplitude bins. # indicate a significant (p < 0.01) main effect of "time" and Bonferronicorrected post-hoc tests *indicate an effect of "time" only in control groups ("group" × "time" p = 0.021).
Scientific Reports | (2021) 11:4758 | https://doi.org/10.1038/s41598-021-83980-w www.nature.com/scientificreports/ of the night (Fig. 2B), with not much change in power further happening over the course of the night. Overall these results may suggest reduced capacity for synaptic potentiation during wake in patients with RBD, which can be sensitively detected by the subsequent alteration in SWA homeostasis during NREM sleep. Sunwoo et al. very recently confirmed abnormalities in the morphology of NREM slow-waves in RBD patients, including decreased amplitude and slopes 67 . Impairments of NREM sleep homeostasis and neuroplasticity have been observed in other patient populations, such as in MDD 68 . However, a pattern encompassing both REM and NREM sleep abnormalities seems unique to RBD patients and was not found in previous MDD literature nor in our MC controls. Future studies in larger groups of patients may clarify potentially differential but cumulative effects of RBD and MDD on NREM sleep homeostasis in medicated and non-medicated subjects.
The mechanisms of the neurodegenerative process in RBD remain unclear. The degeneration of the sublaterodorsal nucleus (SLD) in rodents-equivalent to the coeruleus/subcoeruleus nuclei complex in humansis thought to be implicated in the loss of muscle atonia 69 . However, this pathology does not account for the wide variety of other non-motor symptoms observed in RBD. According to a current theory of RBD, the Braak's ascending model, synuclein deposition in other brainstem nuclei may likely account for other RBD symptoms [70][71][72] . Of particular relevance to interpret the present findings is the evidence for a dysfunction in the central noradrenergic system in RBD patients-thought to be related to locus coeruleus damage. Indeed, brain imaging studies using neuromelanin-sensitive techniques demonstrated reduced signal intensity in the locus coeruleus/subcoeruleus complex in RBD patients 35,36 . Greater deposition of alpha-synuclein in the locus coeruleus (LC) were also found in autopsy specimens from RBD patients 37,38 . Another line of evidence suggesting impaired noradrenergic function in RBD comes from the observation that the amplitude of the event-related potential P300 during a visuospatial attention task-a marker of LC activity 73 -is reduced in RBD patients compared to controls 39 . Because the noradrenergic system plays a crucial role to allow synaptic potentiation during wake and subsequent synaptic homeostasis during sleep, decreased noradrenergic tone in RBD patients may decrease the strength of their brain plasticity processes. This would be in line with animal studies showing that pharmacological depletion of noradrenaline blunted SWA accumulation during wake and subsequent decrease during sleep in mice 40,41 . Our findings may at first contrast with the results of a previous study performed on one central derivation (C3-A2) which found increased SWA during the first three sleep cycles in RBD patients compared to controls, with no differences on SWA changes over the course of the night 74 . However, increased SWA during NREM sleep in their RBD cohort could be accounted by the increased time they spent in N3 stage sleep-while in our study sleep parameters were not different between RBD patients and controls. Additionally, this prior investigation focused on absolute spectral power, and evaluated patients with a mean age nearly 20 years older than our current sample. Future larger studies that provide an ability to examine effects of age on EEG power spectra in RBD may further clarify the predictive power of absolute SWA versus overnight SWA changes as biomarkers predictive of cognitive impairment and of a future conversion to neurodegenerative disorders in RBD patients across mid-life to later adulthood.

Limitations.
One notable shortcoming of our study is its small sample size-which is due to both the retrospective nature of our work and the low prevalence of RBD (0.5-2% of the general population) [75][76][77] . However, our sample size is comparable to other published hdEEG sleep studies in patients with insomnia (n = 8) 56 , obstructive sleep apnea (n = 9) 54 or NREM parasomnias (n = 15) 55 , in which controls were, like in our study, carefully age-and sex-matched.
Our analyses were not restricted to RBD subjects who were free of medications. As such, it more realistically reflects the nature of brain activity changes seen in RBD patients encountered in the sleep clinic. To take into account possible confounding factors, we both verified that the severity of comorbid sleep disorders (sleep apnea and period limb movement disorder indices) was similar between patients and controls and used a second MC group to account for the known effects of SSRIs 78 , benzodiazepines 79 and depression 68 on sleep homeostatic processes. Despite these efforts, our results may not necessarily be generalizable to all RBD patients. Future studies in larger clinical cohorts may assess the relative contribution of medication versus disease severity to EEG changes.
To note, two of our patients may have had anti-depressant related RBD. Current opinions in the field suggest that RBD with antidepressant can be considered as originating from the same underlying alpha-synucleinopathyrelated neurodegeneration process rather than being a separate drug-induced condition 5,71 . Importantly, 8 out of our 9 patients consisted of "early-onset" RBD (onset of symptoms < or = to 50 years of age). This proportion is not anomalous, as in the recent years, it was noticed that RBD population at sleep centers consist of patients of younger age with a more equal representation of both sexes compared to typical RBD 80 . Early-onset RBD has been associated to a higher proportion of females, higher rates of depression and narcolepsy, and a lower rate of neurodegenerative disease such as PD, as opposed to late-onset RBD, more closely linked to elderly men and with a high probability for neurodegenerative diseases [81][82][83] . Age per se is also known to affect sleep SWA [84][85][86] . Our results should thus be interpreted with caution with respect to classical later-onset RBD, and larger cohort studies may in the future be able to assess a potential interaction between age, anti-depressant use and pathophysiologically distinct types of RBD.
Another potential caveat of this study is the single night recording design, which did not allow us to control for potential first-night effects 87,88 . To note, it was recently found that RBD patients are less likely to experience worse sleep during a first PSG night compared to other sleep-disordered patients 89 . Future studies may ideally replicate findings over the course of two nights. Additionally, our cross-sectional design is not able to determine how our observed hdEEG alterations in REM and NREM sleep in RBD participants are related to risk of progression to symptomatic alpha-synucleinopathies. www.nature.com/scientificreports/ Thus, applying hdEEG to longitudinal studies of RBD may be a fruitful area of research, particularly in the future development of preventative strategies for these disorders. Finally, we could not capture high quality wake data to compare to REM sleep and NREM sleep in our RBD patients. Such a comparison would be helpful to quantify within-subject differences in state-dependent SWA across these three states. Future prospective studies may aim to explicitly record a few minutes of full wakefulness before and after sleep in both controls and patients with RBD.

Conclusion and future directions
Our hdEEG study revealed that our sample population of nine RBD patients, predominantly early-onset medicated individuals, display two clinically relevant alterations in brain activity during their sleep: (1) they showed an attenuated suppression of beta activity during phasic REM sleep compared to tonic REM sleep, which may predispose them to motor enactment during phasic REM sub-stage; (2) they showed a reduced overnight decline in SWA during NREM sleep, likely reflecting a decreased capacity for neural plasticity during wake. These findings were reproducible when comparing patients to both medicated and non-medicated controls that were matched for age and sex, and thus quite likely to be an RBD-specific effect.
Taken in the context of previous literature, our results may pave the way to further test the hypothesis that decreased noradrenergic tone during wake may lead to a reduced capacity for plastic changes in patients with RBD, which translates into a decrease in overnight SWA decline. Combined with REM abnormalities, this NREM sleep EEG profile could constitute a sensitive diagnostic biomarker for RBD that can be obtained from paraclinical studies.

Data availability
The datasets generated during and/or analyzed during the current study are available from the corresponding author upon reasonable request.