Evidence map›Paper›PMID 41972109›Full record

ArticleFrontiers in aging neuroscience2026

Amantadine-based combination therapy of Parkinson's disease to prevent fluctuation and dyskinesia - experiences from a Parkinson outpatient clinic.

Christian Oehlwein, Lucas Netzel, Katrin Mittmann, Marita Oehlwein, Walter J Schulz-Schaeffer

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Article in Frontiers in aging neuroscience, 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

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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

5 authors.

Christian Oehlwein *Parkinson's Disease Outpatient Clinic, Gera, Germany.
Lucas Netzel *Parkinson's Disease Outpatient Clinic, Gera, Germany.
Katrin MittmannParkinson's Disease Outpatient Clinic, Gera, Germany.
Marita OehlweinParkinson's Disease Outpatient Clinic, Gera, Germany.
Walter J Schulz-SchaefferDepartment of Neuropathology, University of the Saarland, Homburg/Saar, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The standard therapy of Parkinson's disease consists in supplementing the depleted dopamine with oral levodopa. The disadvantages of the levodopa monotherapy - comparable to other dopaminergic substances - are the dose-dependent development of dyskinesia in ON-phases, and bradykinesia and akinesia in OFF-phases, the latter being a sign of dopaminergic deficiency with a recurrence of Parkinson's symptoms. Aim of the study: In order to omit the side effects of levodopa, we devised a combination therapy consisting of amantadine, a monoamine oxidase type B-inhibitor and a dopamine agonist. Levodopa was added at a low dose, if necessary. Methods: In a retrospective, monocenter study based on the patient records, we report the long-term results in 132 PD patients who had been treated with the amantadine-based therapy for up to 13 years in an outpatient Parkinson clinic. Results: In 132 patients with the amantadine-based combination therapy, the mean UPDRS III score improved by 5.7 points from baseline during the first 2 years of treatment. Over the following 3 years it increased and remained at a plateau level slightly below baseline for the next 5 years. At no time did more than 20% of the patients suffer from Hoehn & Yahr stage 3 or higher. Only seven patients exhibited "OFF" periods and only seven (6 with additional levodopa) presented with dyskinesia at any time during therapy. The most important adverse effect was lower leg edema. Conclusion: The combination therapy of amantadine, a monoamine oxidase type B-inhibitor and a dopamine agonist is an alternate therapeutic approach that may be able to prevent dyskinesia and fluctuations by drug pharmacokinetics and synergistic effects, and may postpone or reduce the amount of levodopa. Prospective controlled studies are needed to compare the effects of the amantadine-based combination therapy with the standard levodopa therapy for Parkinson's disease.

Indexed as

amantadinedopamine agonistdyskinesiafluctuationlevodopaMAO type B-inhibitor

Identifiers

PMID41972109
PMCPMC13062172

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