Evidence map›Paper›PMID 36964457›Full record

ReviewJournal of neural transmission (Vienna, Austria : 1996)2023

Clinical benefit of MAO-B and COMT inhibition in Parkinson's disease: practical considerations.

Martin Regensburger, Chi Wang Ip, Zacharias Kohl, Christoph Schrader, Peter P Urban, Jan Kassubek, Wolfgang H Jost

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of neural transmission (Vienna, Austria : 1996), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 2 pooled it
13.6field-weighted citation impact, top 1% 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

42 citing papers in PubMed, 2 syntheses or guidelines pooled it, 66 citations in OpenAlex.

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  14. Neuroprotective role ofFrontiers in nutrition · 2026
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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

7 authors at 7 institutions in 1 country.

Martin RegensburgerDepartment of Molecular Neurology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany. martin.regensburger@uk-erlangen.de.ORCID http://orcid.org/0000-0002-2172-7386
Chi Wang IpDepartment of Neurology, University Hospital of Würzburg, Würzburg, Germany.ORCID http://orcid.org/0000-0003-0484-385X
Zacharias KohlDepartment of Neurology, University of Regensburg, Regensburg, Germany.ORCID http://orcid.org/0000-0002-4147-8866
Christoph SchraderDepartment of Neurology, Hannover Medical School, Hannover, Germany.ORCID http://orcid.org/0000-0001-5323-8299
Peter P UrbanAbt. für Neurologie, Asklepios Klinik Barmbek, Hamburg, Germany.ORCID http://orcid.org/0000-0002-4899-1937
Jan KassubekDepartment of Neurology, University Hospital Ulm, Ulm, Germany.ORCID http://orcid.org/0000-0002-7106-9270
Wolfgang H JostParkinson-Klinik Ortenau, Wolfach, Germany.ORCID http://orcid.org/0000-0002-8574-3297
Asklepios Klinik Barmbek · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEMedizinische Hochschule Hannover · DEParkinson-Klinik Ortenau · DEUniversitätsklinikum Würzburg · DEUniversity Hospital Ulm · DEUniversity of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inhibitors of monoamine oxidase B (MAO-B) and catechol-O-methyltransferase (COMT) are major strategies to reduce levodopa degradation and thus to increase and prolong its effect in striatal dopaminergic neurotransmission in Parkinson's disease patients. While selegiline/rasagiline and tolcapone/entacapone have been available on the market for more than one decade, safinamide and opicapone have been approved in 2015 and 2016, respectively. Meanwhile, comprehensive data from several post-authorization studies have described the use and specific characteristics of the individual substances in clinical practice under real-life conditions. Here, we summarize current knowledge on both medication classes, with a focus on the added clinical value in Parkinson's disease. Furthermore, we outline practical considerations in the treatment of motor fluctuations and provide an outlook on ongoing studies with MAO-B and COMT inhibitors.

Indexed as

Parkinson DiseaseAntiparkinson AgentsCatechol O-MethyltransferaseCatechol O-Methyltransferase InhibitorsHumansLevodopaMonoamine OxidaseMonoamine Oxidase InhibitorsAntiparkinson AgentsCatechol O-MethyltransferaseCatechol O-Methyltransferase InhibitorsCOMT protein, humanLevodopaMonoamine OxidaseMonoamine Oxidase InhibitorsCOMT inhibitorsMAO-B inhibitorsMotor fluctuationsParkinson’s disease

Identifiers

PMID36964457
PMCPMC10199833
OpenAlexW4360830166

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.