Impulse Control Disorders and Levodopa-Induced Dyskinesias in Parkinson's Disease: Pulsatile versus Continuous Dopaminergic Stimulation.


Journal

Journal of Parkinson's disease
ISSN: 1877-718X
Titre abrégé: J Parkinsons Dis
Pays: Netherlands
ID NLM: 101567362

Informations de publication

Date de publication:
2020
Historique:
pubmed: 14 4 2020
medline: 20 8 2021
entrez: 14 4 2020
Statut: ppublish

Résumé

Dopaminergic medications in Parkinson's disease (PD) are usually associated with the development of both levodopa-induced dyskinesias (LID) and impulse control and repetitive behavior disorders (ICRB). To assess the prevalence and the severity of ICRB in a cohort of moderate and advanced PD patients and to investigate the potential interplay between ICRB, LID and dopaminergic therapies. 117 PD patients were consecutively recruited. LID were assessed by using the Rush Dyskinesia Rating Scale (RDRS). ICRB were tested by means of Questionnaire for Impulsive Compulsive Disorders in Parkinson's Disease Rating Scale (QUIP-RS). 55 patients were affected by LID. Among them, 37 were treated only by oral therapy, OT (LID/OT), while 18 were on treatment with jejunal levodopa infusion, JLI (LID/JLI). 62 patients were not affected by LID (NLID) and all of them were on therapy only with oral drugs. The overall prevalence of clinically significant ICRB was 34% (95% CI = 26% to 43%) and the mean value (±SD) of QUIP-RS total score was 5.4±8.5. Prevalence of clinically significant ICRB, as well as severity of ICRB, was higher in patients with LID compared to NLID patients (p = 0.016 and p < 0.001, respectively). When considering LID/JLI, LID/OT and NLID groups, QUIP-RS total score was significantly higher in LID/OT patients compared to LID/JLI (10.4±11.8 vs. 4.9±6.0, p = 0.019) and NLID (10.4±11.8 vs. 2.5±4.8, p < 0.001) groups. PD patients with LID show ICRB more frequently and more severely than patients without LID. Among LID patients, those treated by JLI showed a lower severity of ICRB than those on OT, suggesting a potential protective effect of JLI on ICRB.

Sections du résumé

BACKGROUND
Dopaminergic medications in Parkinson's disease (PD) are usually associated with the development of both levodopa-induced dyskinesias (LID) and impulse control and repetitive behavior disorders (ICRB).
OBJECTIVE
To assess the prevalence and the severity of ICRB in a cohort of moderate and advanced PD patients and to investigate the potential interplay between ICRB, LID and dopaminergic therapies.
METHODS
117 PD patients were consecutively recruited. LID were assessed by using the Rush Dyskinesia Rating Scale (RDRS). ICRB were tested by means of Questionnaire for Impulsive Compulsive Disorders in Parkinson's Disease Rating Scale (QUIP-RS).
RESULTS
55 patients were affected by LID. Among them, 37 were treated only by oral therapy, OT (LID/OT), while 18 were on treatment with jejunal levodopa infusion, JLI (LID/JLI). 62 patients were not affected by LID (NLID) and all of them were on therapy only with oral drugs. The overall prevalence of clinically significant ICRB was 34% (95% CI = 26% to 43%) and the mean value (±SD) of QUIP-RS total score was 5.4±8.5. Prevalence of clinically significant ICRB, as well as severity of ICRB, was higher in patients with LID compared to NLID patients (p = 0.016 and p < 0.001, respectively). When considering LID/JLI, LID/OT and NLID groups, QUIP-RS total score was significantly higher in LID/OT patients compared to LID/JLI (10.4±11.8 vs. 4.9±6.0, p = 0.019) and NLID (10.4±11.8 vs. 2.5±4.8, p < 0.001) groups.
CONCLUSION
PD patients with LID show ICRB more frequently and more severely than patients without LID. Among LID patients, those treated by JLI showed a lower severity of ICRB than those on OT, suggesting a potential protective effect of JLI on ICRB.

Identifiants

pubmed: 32280105
pii: JPD191833
doi: 10.3233/JPD-191833
doi:

Substances chimiques

Dopamine Agents 0
Levodopa 46627O600J

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

927-934

Auteurs

Simone Simoni (S)

Movement Disorders Center, Neurology Department, Perugia General Hospital and University of Perugia, Perugia, Italy.

Federico Paolini Paoletti (FP)

Movement Disorders Center, Neurology Department, Perugia General Hospital and University of Perugia, Perugia, Italy.
Neurology Department, Perugia General Hospital and University of Perugia, Perugia, Italy.

Paolo Eusebi (P)

Neurology Department, Perugia General Hospital and University of Perugia, Perugia, Italy.

Giulia Cappelletti (G)

Neurology Department, Perugia General Hospital and University of Perugia, Perugia, Italy.

Marta Filidei (M)

Neurology Department, Perugia General Hospital and University of Perugia, Perugia, Italy.

Elona Brahimi (E)

Neurology Department, Regina Montis Regalis Hospital, Cuneo, Italy.

Pasquale Nigro (P)

Movement Disorders Center, Neurology Department, Perugia General Hospital and University of Perugia, Perugia, Italy.

Valerio Santangelo (V)

Department of Philosophy, Social Sciences & Education, University of Perugia, Perugia, Italy.
Neuroimaging Laboratory, IRCCS Santa Lucia Foundation, Rome, Italy.

Lucilla Parnetti (L)

Neurology Department, Perugia General Hospital and University of Perugia, Perugia, Italy.
Section of Neurology Department, Center for Memory Disturbances, Laboratory of Clinical Neurochemistry, Perugia General Hospital and University of Perugia, Perugia, Italy.

Paolo Calabresi (P)

Neurologia, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, Italy.

Nicola Tambasco (N)

Movement Disorders Center, Neurology Department, Perugia General Hospital and University of Perugia, Perugia, Italy.
Neurology Department, Perugia General Hospital and University of Perugia, Perugia, Italy.

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