Evidence map›Paper›PMID 35774903›Full record

ArticleHealth psychology research2022

Opicapone, a Novel Catechol-O-methyl Transferase Inhibitor, for Treatment of Parkinson's Disease "Off" Episodes.

Amnon A Berger, Ariel Winnick, Jonathan Izygon, Binil M Jacob, Jessica S Kaye, Rachel J Kaye, Elisa E Neuchat, Adam M Kaye, Edward S Alpaugh, Elyse M Cornett and 2 more

Open access · goldAbstract read
In one paragraph

Article in Health psychology research, 2022. 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
0.9field-weighted citation impact, top 26% of its field
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, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
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

12 authors at 9 institutions in 2 countries.

Amnon A BergerAnesthesiology, Critical Care, and Pain Medicine, Beth Israel Deaconess Medical Center.
Ariel WinnickSoroka University Medical Center and Faculty of Health Sciences; School of Optometry, University of California.
Jonathan IzygonSoroka University Medical Center and Faculty of Health Sciences.
Binil M JacobSoroka University Medical Center and Faculty of Health Sciences.
Jessica S KayeDepartment of Pharmacy Practice, Thomas J. Long School of Pharmacy and Health Sciences, University of the Pacific.
Rachel J KayeMedical University of South Carolina.
Elisa E NeuchatFlorida International University.
Adam M KayeDepartment of Pharmacy Practice, Thomas J. Long School of Pharmacy and Health Sciences, University of the Pacific.
Edward S AlpaughDepartment of Anesthesiology, Louisiana State University Health Sciences Center.
Elyse M CornettDepartment of Anesthesiology, Louisiana State University Health Sciences Center.
Andrew H HanGeorgetown University School of Medicine, Georgetown University School of Medicine.
Alan D KayeDepartment of Anesthesiology, Louisiana State University Health Sciences Center.
University of the Pacific · USLouisiana State University Health Sciences Center New Orleans · USFlorida International University · USGeorgetown University · USHadassah Medical Center · ILMedical University of South Carolina · USSoroka Medical Center · ILUniversity Hospital and Clinics · USUniversity Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's Disease (PD) is a common neurodegenerative disorder and the leading cause of disability. It causes significant morbidity and disability through a plethora of symptoms, including movement disorders, sleep disturbances, and cognitive and psychiatric symptoms. The traditional pathogenesis theory of PD involves the loss of dopaminergic neurons in the substantia nigra (SN). Classically, treatment is pursued with an assortment of medications that are directed at overcoming this deficiency with levodopa being central to most treatment plans. Patients taking levodopa tend to experience "off episodes" with decreasing medication levels, causing large fluctuations in their symptoms. These off episodes are disturbing and a source of morbidity for these patients. Opicapone is a novel, peripherally acting Catechol-O-methyl transferase (COMT) inhibitor that is used as adjunctive therapy to carbidopa/levodopa for treatment and prevention of "off episodes." It has been approved for use as an adjunct to levodopa since 2016 in Europe and has recently (April 2020) gained FDA approval for use in the USA. By inhibiting COMT, opicapone slows levodopa metabolism and increases its availability. Several clinical studies demonstrated significant improvement in treatment efficacy and reduction in duration of "off episodes." The main side effect demonstrated was dyskinesia, mostly with the 100mg dose, which is higher than the approved, effective dose of 50mg. Post-marketing surveillance and analysis are required to further elucidate its safety profile and contribute to patient selection. This paper reviews the seminal and latest evidence in the treatment of PD "off episodes" with the novel drug Opicapone, including efficacy, safety, and clinical indications.

Indexed as

COMTlevodopaneurodegenerativeOpicaponeparkinsonismrigidity

Identifiers

PMID35774903
PMCPMC9239372
OpenAlexW4283661848

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.