Evidence map›Paper›PMID 42133014›Full record

ArticleJournal of neural transmission (Vienna, Austria : 1996)2026

Treatment stability comparison among different ADD-ON therapies in fluctuating Parkinson's disease patients: the role of clinical and demographic factors.

Domiziana Rinaldi, Silvia Galli, Gabriele Imbalzano, Serena Budicin, Edoardo Bianchini, Lanfranco De Carolis, Claudia Ledda, Pierre Pacilio, Maurizio Zibetti, Marika Alborghetti and 3 more

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Article in Journal of neural transmission (Vienna, Austria : 1996), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Domiziana RinaldiDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), Sapienza University of Rome, Via di Grottarossa, 1035, Rome, 00189, Italy. domiziana.rinaldi@uniroma1.it.
Silvia GalliDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), Sapienza University of Rome, Via di Grottarossa, 1035, Rome, 00189, Italy.
Gabriele ImbalzanoDepartment of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
Serena BudicinDepartment of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
Edoardo BianchiniDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), Sapienza University of Rome, Via di Grottarossa, 1035, Rome, 00189, Italy.
Lanfranco De CarolisDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), Sapienza University of Rome, Via di Grottarossa, 1035, Rome, 00189, Italy.
Claudia LeddaDepartment of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
Pierre PacilioDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), Sapienza University of Rome, Via di Grottarossa, 1035, Rome, 00189, Italy.
Maurizio ZibettiDepartment of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
Marika AlborghettiDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), Sapienza University of Rome, Via di Grottarossa, 1035, Rome, 00189, Italy.
Francesco Ernesto PontieriDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), Sapienza University of Rome, Via di Grottarossa, 1035, Rome, 00189, Italy.
Carlo Alberto ArtusiDepartment of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.
Leonardo LopianoDepartment of Neuroscience "Rita Levi Montalcini", University of Turin, Turin, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMotor fluctuations represent a major challenge in Parkinson's disease (PD) management. To address them, ADD-ON therapies with monoamine oxidase type B (MAO-B) and catechol-O-methyl transferase (COMT) inhibitors are used to enhance and prolong dopaminergic effects of levodopa, thereby improving motor fluctuations. Despite widespread use, real-life comparative data remain limited.

methodsWe performed a retrospective, longitudinal study including PD patients referred to two Italian tertiary movement disorder centers. Patients with motor fluctuations requiring ADD-ON therapy (selegiline [SL], rasagiline [RS], safinamide [SF], or opicapone [OP]) and ≥ 12 months of follow-up were included. The primary outcome was treatment stability, defined as months without significant therapy modifications or ADD-ON discontinuation. Secondary outcomes included levodopa dosage changes, initiation of other antiparkinsonian therapies, and ADD-ON discontinuation rates. Cox regression models and Kaplan-Meier survival analyses evaluated the influence of ADD-ON type and clinical-demographic variables on treatment stability.

resultsWe analyzed 169 patients (SL = 20; RS = 26; SF = 78; OP = 45). Groups differed in age at ADD-ON initiation (p = 0.020; RS > OP), disease duration (p = 0.002; OP > RS and SF), and baseline levodopa equivalent daily dose (p = 0.003; SF and OP > RS). No significant differences in treatment stability were found between groups (p = 0.29). SF group showed higher levodopa increases (p = 0.02) and initiation of new therapies (p = 0.02). ADD-ON discontinuation occurred in 23.1% of patients, mainly due to AEs (16.6%). Cox regression showed no significant predictors of treatment stability.

conclusionsAll ADD-ON therapies showed comparable treatment stability and tolerability. No statistically significant sex-related differences were observed, although a trend toward more frequent therapy modifications was found in female patients.

Indexed as

Antiparkinsonian therapyCOMT inhibitorsMAOB inhibitorsParkinson’s diseaseWearing-off

Identifiers

PMID42133014

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.