Association between dopaminergic medications and REM sleep behavior disorder in Parkinson's disease: a preliminary cohort study.

Dopamine-replacement therapies Levodopa equivalency daily dose Parkinson's disease REM sleep behavior disorder

Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 27 04 2020
accepted: 26 05 2020
revised: 24 05 2020
pubmed: 31 5 2020
medline: 21 5 2021
entrez: 31 5 2020
Statut: ppublish

Résumé

Rapid eye movement sleep behavior disorder (RBD) is highly comorbid with Parkinson's disease (PD). Emerging evidence suggests that dopamine-replacement therapies (DRTs) for PD may modify the course of RBD, yet the nature of the association between DRTs and RBD remains unclear. To begin addressing this issue, we conducted a preliminary retrospective study to document whether DRTs are associated with the occurrence of RBD symptoms in PD patients. The study included 250 PD patients who were screened for probable RBD via the RBD Screening Questionnaire (RBDSQ). For each patient, disease severity data were collected, in addition to their therapy and the associated levodopa equivalent daily dose (LEDD). The association between DRTs and RBDSQ scores was analyzed using logistic regression and correlation models. RBD scores were found to be associated with the LEDD of levodopa alone, but not of dopaminergic agonists (mainly D2/D3 receptor agonists) or their combination with levodopa. This association was not accounted for patient age or Hoehn and Yahr (H&Y) severity scores. Our study detected a significant association between doses of levodopa and RBD symptoms in PD patients. Future longitudinal studies are needed to establish what causal nexus may link these variables.

Sections du résumé

BACKGROUND BACKGROUND
Rapid eye movement sleep behavior disorder (RBD) is highly comorbid with Parkinson's disease (PD). Emerging evidence suggests that dopamine-replacement therapies (DRTs) for PD may modify the course of RBD, yet the nature of the association between DRTs and RBD remains unclear. To begin addressing this issue, we conducted a preliminary retrospective study to document whether DRTs are associated with the occurrence of RBD symptoms in PD patients.
METHODS METHODS
The study included 250 PD patients who were screened for probable RBD via the RBD Screening Questionnaire (RBDSQ). For each patient, disease severity data were collected, in addition to their therapy and the associated levodopa equivalent daily dose (LEDD). The association between DRTs and RBDSQ scores was analyzed using logistic regression and correlation models.
RESULTS RESULTS
RBD scores were found to be associated with the LEDD of levodopa alone, but not of dopaminergic agonists (mainly D2/D3 receptor agonists) or their combination with levodopa. This association was not accounted for patient age or Hoehn and Yahr (H&Y) severity scores.
CONCLUSIONS CONCLUSIONS
Our study detected a significant association between doses of levodopa and RBD symptoms in PD patients. Future longitudinal studies are needed to establish what causal nexus may link these variables.

Identifiants

pubmed: 32472180
doi: 10.1007/s00415-020-09956-4
pii: 10.1007/s00415-020-09956-4
doi:

Substances chimiques

Levodopa 46627O600J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2926-2931

Auteurs

Mario Meloni (M)

IRCCS, Fondazione Don Carlo Gnocchi, Milan, Italy.

Marco Bortolato (M)

Department of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, UT, USA.

Antonino Cannas (A)

Department of Medical Sciences and Public Health, Neurology Unit, University of Cagliari and AOU Cagliari, Monserrato, Cagliari, Italy.

Ilaria Laccu (I)

Sleep Disorder Research Center, Department of Medical Science and Public Health, University of Cagliari, Asse didattico E SS 554, Bivio Sestu, 09042, Monserrato, Cagliari, Italy.

Michela Figorilli (M)

Sleep Disorder Research Center, Department of Medical Science and Public Health, University of Cagliari, Asse didattico E SS 554, Bivio Sestu, 09042, Monserrato, Cagliari, Italy.

Patrizia Congiu (P)

Sleep Disorder Research Center, Department of Medical Science and Public Health, University of Cagliari, Asse didattico E SS 554, Bivio Sestu, 09042, Monserrato, Cagliari, Italy.

Giovanni Defazio (G)

Department of Medical Sciences and Public Health, Neurology Unit, University of Cagliari and AOU Cagliari, Monserrato, Cagliari, Italy.

Federico Meloni (F)

Occupational Health Section, Department of Medical Science and Public Health, University of Cagliari, Cagliari, Italy.

Monica Puligheddu (M)

Department of Medical Sciences and Public Health, Neurology Unit, University of Cagliari and AOU Cagliari, Monserrato, Cagliari, Italy. puligheddu@unica.it.
Sleep Disorder Research Center, Department of Medical Science and Public Health, University of Cagliari, Asse didattico E SS 554, Bivio Sestu, 09042, Monserrato, Cagliari, Italy. puligheddu@unica.it.

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Classifications MeSH