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Efficacy and safety of adjunctive oral therapy in Parkinson's disease with motor complications: a systematic review and network meta-analysis.
Sisodia, Vibuthi; Dubbeld, Lars; De Bie, Rob M A; Duarte, Gonçalo S; Costa, João; Dijk, Joke M.
  • Sisodia V; Neurology, Amsterdam UMC Location AMC, Amsterdam, The Netherlands.
  • Dubbeld L; Amsterdam Neuroscience, Neurodegeneration, Amsterdam, the Netherlands.
  • De Bie RMA; Neurology, Amsterdam UMC Location AMC, Amsterdam, The Netherlands.
  • Duarte GS; Neurology, Amsterdam UMC Location AMC, Amsterdam, The Netherlands.
  • Costa J; Amsterdam Neuroscience, Neurodegeneration, Amsterdam, the Netherlands.
  • Dijk JM; Clinical Pharmacology Department, Hospital da Luz, Lisboa, Portugal.
BMJ Neurol Open ; 6(1): e000573, 2024.
Article en En | MEDLINE | ID: mdl-38352047
ABSTRACT

Background:

The aim of this manuscript is to review the evidence and compare the efficacy and safety of catechol-O-methyltransferase inhibitors (COMT-Is), dopamine receptor agonists (DRAs) and monoamine-oxidase B inhibitors (MAOB-Is) as adjunctive treatment to levodopa in patients with Parkinson's disease (PD) experiencing motor complications.

Methods:

In this systematic review and network meta-analysis, literature searches were performed in MEDLINE and Embase to identify eligible randomised controlled trials (RCTs) with a minimal follow-up of at least 4 weeks published in English between 1980 and 2021. RCTs were included if either a COMT-I, DRA or MAOB-I was evaluated as an adjunctive therapy to levodopa in patients with PD experiencing motor complications and dyskinesia. The main outcomes included daily off-medication time, motor and non-motor examination scales, and adverse events including dyskinesia.

Results:

74 RCTs reporting on 18 693 patients were included. All three studied drug classes decreased daily off-medication time compared with placebo (COMT-Is mean -0.8 hours (95% CI -1.0 to -0.6), DRAs -1.1 hours (95% CI -1.4 to -0.8), MAOB-Is -0.9 hours (95% CI -1.2 to -0.6)). Safety analysis showed an increased risk of dyskinesia for all three drug classes (COMT-Is OR 3.3 (95% CI 2.7 to 4.0), DRAs 3.0 (95% CI 2.5 to 3.5), MAOB-Is 1.6 (95% CI 1.2 to 2.2)). According to surface under the cumulative ranking curve scores, pramipexole IR was associated with the most favourable benefit-risk profile.

Conclusions:

COMT-Is, DRAs and MAOB-Is effectively reduce motor complications and increase incidence of dyskinesia. In the network meta-analysis, adjunctive use of DRAs appeared most effective.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies / Systematic_reviews Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies / Systematic_reviews Idioma: En Año: 2024 Tipo del documento: Article