Evidence map›Paper›PMID 40886228›Full record

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

Opicapone in Parkinson's disease: a real-world, multicenter, retrospective study to identify patient characteristics for sustained treatment benefit.

Clelia Pellicano, Daniele Belvisi, Roberta Bovenzi, Matteo Costanzo, Maria I De Bartolo, Francesca Sommaruga, Jessica Blandino, Nicola Modugno, Fabrizio Piras, Mariangela Pierantozzi and 3 more

Abstract readMulticenter Study
In one paragraph

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. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Clelia PellicanoLaboratory of Neuropsychiatry, Santa Lucia Foundation IRCCS, Rome, Italy.
Daniele BelvisiDepartment of Human Neurosciences, Sapienza University of Rome, Rome, Italy. daniele.belvisi@uniroma1.it.
Roberta BovenziUnit of Neurology, Department of Systems Medicine, Tor Vergata University of Rome, Rome, Italy.
Matteo CostanzoDepartment of Human Neurosciences, Sapienza University of Rome, Rome, Italy.
Maria I De BartoloDepartment of Human Neurosciences, Sapienza University of Rome, Rome, Italy.
Francesca SommarugaLaboratory of Neuropsychiatry, Santa Lucia Foundation IRCCS, Rome, Italy.
Jessica BlandinoLaboratory of Neuropsychiatry, Santa Lucia Foundation IRCCS, Rome, Italy.
Nicola ModugnoDepartment of Neurology and Clinical Neurophysiology, IRCCS Neuromed, Pozzilli, Italy.
Fabrizio PirasLaboratory of Neuropsychiatry, Santa Lucia Foundation IRCCS, Rome, Italy.
Mariangela PierantozziUnit of Neurology, Department of Systems Medicine, Tor Vergata University of Rome, Rome, Italy.
Alessandro StefaniUnit of Neurology, Department of Systems Medicine, Tor Vergata University of Rome, Rome, Italy.
Giovanni FabbriniDepartment of Human Neurosciences, Sapienza University of Rome, Rome, Italy.
Tommaso SchirinziUnit of Neurology, Department of Systems Medicine, Tor Vergata University of Rome, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fluctuations often complicate the course of Parkinson's disease (PD). The third-generation catechol-O-methyltransferase inhibitor, opicapone, is safe and effective in patients with PD motor fluctuations, whether long-standing or earlier onset. Real-world data are needed to identify the most appropriate candidates for initiating and sustaining therapy with opicapone. To evaluate the long-term outcomes and identify predictors for safer and prolonged use of opicapone. This real-world, longitudinal, multicenter, retrospective study collected data on the demographics, medical history, motor subtype, motor severity, cognitive and psychiatric disorders at baseline when opicapone was introduced as add-on therapy and at the last follow-up. Discontinuation rates and main causes were recorded. Clinical features of patients who continued/discontinued were compared to identify predictors for drug discontinuation and define successful long-term outcomes. Of the 178 enrolled patients, 85% (35% of them female) continued opicapone for a mean of 30.2 ± 19.64 months. The remaining 15% (13.4% female) discontinued opicapone within 8.9 ± 11.30 months due to disabling dyskinesia, hypotension, gastrointestinal disorders, or psychiatric disturbances. Continuers were younger at baseline than those who discontinued, but clinical-demographic features did not predict continuing opicapone therapy. Continuers had significantly lower Hoehn and Yahr scale scores and fewer night-time OFF periods compared with discontinuers, whereas levodopa equivalent daily dose and burden of motor and neuropsychiatric complications were similar. Continued opicapone therapy was associated with less motor impairment and reduced night-time OFF. Safety and long-term tolerability were higher in younger patients with a tendency to milder motor severity.

Indexed as

Antiparkinson AgentsCatechol O-Methyltransferase InhibitorsOxadiazolesParkinson DiseaseAgedFemaleHumansLongitudinal StudiesMaleMiddle AgedRetrospective StudiesTreatment OutcomeAntiparkinson AgentsCatechol O-Methyltransferase InhibitorsopicaponeOxadiazolesCatechol-O-methyltransferase inhibitorEnd-of-dose wearing offLevodopaMotor fluctuationsOFF timeOpicaponeParkinson’s disease

Identifiers

PMID40886228
PMCPMC12999617

What OpenQuestion holds

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Registered trials

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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.