2018
DOI: 10.1111/ene.13567
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Rasagiline improves polysomnographic sleep parameters in patients with Parkinson's disease: a double‐blind, baseline‐controlled trial

Abstract: In patients with PD with sleep disturbances, rasagiline showed beneficial effects on sleep quality as measured by polysomnography. These effects were probably not related to motor improvement or translated into improved overall sleep quality perception by patients.

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Cited by 28 publications
(30 citation statements)
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“…A double-blind, baseline-controlled study found that rasagiline may be beneficial to the sleep quality of PD patients with sleep disturbance. [34] Based on the result of the study, rasagiline is likely efficacious in improving insomnia in patients with PD.…”
Section: Insomniamentioning
confidence: 99%
“…A double-blind, baseline-controlled study found that rasagiline may be beneficial to the sleep quality of PD patients with sleep disturbance. [34] Based on the result of the study, rasagiline is likely efficacious in improving insomnia in patients with PD.…”
Section: Insomniamentioning
confidence: 99%
“…SDB (cutoff AHI > 5/h) was detected in 73% of patients ( Supplementary Table S1 ) with 46% (12/26) of our patients classified as suffering from mild to moderate sleep-related breathing disorder (SDB, AHI > 5/h ≤ 15/h), whereas 27% (7/26) were found to have moderate SDB (AHI > 15/h ≤ 30/h). Patients with severe SDB (AHI > 30/h) were not recruited into the study according to the predefined exclusion criteria ( Schrempf et al, 2018 ).…”
Section: Resultsmentioning
confidence: 99%
“…From 29 patients initially enrolled between 2011 and 2014, two were excluded due to cognitive impairment [Parkinson Neuropsychometric Dementia Assessment (PANDA) score <18] and one due to diagnostic precariousness, thus, 26 PD patients were included in the analysis. Patients fulfilling PSG exclusion criteria {e.g., severe SDB [Apnea-Hypopnea Index (AHI) >30/h]} and patients with signs of atypical parkinsonian syndromes, deep brain stimulation, severe depression [Montgomery–Asberg Depression Scale (MADRS) >34], severe dementia, or other medical conditions interfering with study procedures as well as patients on medication influencing sleep, e.g., hypnotics and antidepressants, were excluded from the study [for details, please refer to Schrempf et al (2018) ]. Patients had to be on stable antiparkinsonian medication for at least 4 weeks prior to study inclusion.…”
Section: Methodsmentioning
confidence: 99%
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“…Firstly, the replacement of lost dopamine with dopaminergic drugs in 24 is necessary. Adjunctive medications [33][34][35], infusion systems such as DuoDopa (carbidopa/levodopa) [36], continuous dopamine delivery treatments like the transdermal rotigotine patch [37][38][39][40][41], and oral extended release versions of dopamine agents [42,43] have shown signi cant promise in ameliorating wearing-off effects and symptom uctuations, in nocturnal as well as daytime symptoms. In a randomized, placebo-controlled study (the RECOVER trial, quality score, 93%), patients with unsatisfactory control of early morning motor symptoms were evaluated on the PDSS-2 and UPDRS III.…”
Section: Implications For Managing Nocturnal Symptomsmentioning
confidence: 99%