Evidence map›Paper›PMID 38578434›Full record

ArticleJournal of neural transmission (Vienna, Austria : 1996)2024

Amantadine use in the French prospective NS-Park cohort.

Margherita Fabbri, Vanessa Rousseau, Jean-Christophe Corvol, Agnès Sommet, Florence Tubach, Yann De Rycke, Nathalie Bertille, Yajiththa Selvarasa, Stephanie Carvalho, Véronique Chaigneau and 27 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Journal of neural transmission (Vienna, Austria : 1996), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Observational
  2. Article
  3. 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

37 authors at 18 institutions in 3 countries.

Margherita FabbriDepartment of Clinical Pharmacology and Neurosciences, Clinical Investigation Center CIC1436, Toulouse Parkinson Expert Centre, Toulouse NeuroToul Center of Excellence in Neurodegeneration (COEN), University of Toulouse 3, CHU of Toulouse, INSERM, Toulouse, France. margheritafabbrimd@gmail.com.ORCID 0000-0001-7250-592X
Vanessa RousseauDepartment of Clinical Pharmacology, Clinical Investigation Center CIC1436, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.
Jean-Christophe CorvolFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Agnès SommetDepartment of Clinical Pharmacology, Clinical Investigation Center CIC1436, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.
Florence TubachSorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpital Pitié Salpêtrière, Département de Santé Publique, Centre de Pharmacoépidémiologie (Cephepi), Unité de Recherche Clinique PSL-CFX, CIC-1901, F75013, Paris, France.
Yann De RyckeSorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpital Pitié Salpêtrière, Département de Santé Publique, Centre de Pharmacoépidémiologie (Cephepi), Unité de Recherche Clinique PSL-CFX, CIC-1901, F75013, Paris, France.
Nathalie BertilleSorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpital Pitié Salpêtrière, Département de Santé Publique, Centre de Pharmacoépidémiologie (Cephepi), Unité de Recherche Clinique PSL-CFX, CIC-1901, F75013, Paris, France.
Yajiththa SelvarasaFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Stephanie CarvalhoFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Véronique ChaigneauFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Christine Brefel-CourbonFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Fabienne Ory-MagneFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Samuel TessierService de Pharmacologie Médicale et Clinique, Centre Hospitalier Universitaire-Faculté de Médecine, Toulouse, France.
Melissa TirFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Matthieu BereauFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Wassilios G MeissnerFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Claire ThiriezFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Ana MarquesFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Philippe RemyFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Vincent SchneiderFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Elena MoroFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Luc DefebvreFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Jean Luc HouetoFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Stephane PrangeFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Alexandre EusebioFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Christian GenyFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Solène FrismandFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Philippe DamierFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Caroline Giordana ReutherFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Giovanni CastelnovoFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Isabelle BenatruFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Anne Doe De MaindrevilleFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Sophie DrapierFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
David MaltêteFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Ouhaid Lagha-BoukbizaFrench NS-PARK/F-CRIN Network, Clermont-Ferrand, France.
Olivier RascolDepartment of Clinical Pharmacology and Neurosciences, Clinical Investigation Center CIC1436, Toulouse Parkinson Expert Centre, Toulouse NeuroToul Center of Excellence in Neurodegeneration (COEN), University of Toulouse 3, CHU of Toulouse, INSERM, Toulouse, France.
French N. S.-Park network
Inserm · FRCentre National de la Recherche Scientifique · FRCentre Hospitalier Universitaire de Reims · FRCentre Hospitalier Universitaire de Toulouse · FRUniversité Claude Bernard Lyon 1 · FRAssistance Publique Hôpitaux de Marseille · FRFrench Clinical Research Infrastructure Network · FRUniversité de Bourgogne · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Universitaire Amiens-Picardie · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Caen Normandie · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Nîmes · FRUniversité Clermont Auvergne · FRUniversité Côte d'Azur · FRUniversité de Caen Normandie · FRUniversité de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess amantadine use and associated factors in the patients with Parkinson's disease (PD).

backgroundImmediate-release amantadine is approved for the treatment of PD and is largely used in clinical practice to treat "levodopa-induced dyskinesia (LIDs). Its use varies according to countries and PD stages. The prospective NS-Park cohort collects features of PD patients followed by 26 French PD Expert Centres.

methodsVariables used for the analyses included demographics, motor and non-motor PD symptoms and motor complications [motor fluctuations (MFs), LIDs)], antiparkinsonian pharmacological classes and levodopa equivalent daily dose (LEDD). We evaluated: (i) prevalence of amantadine use and compared clinical features of amantadine users vs. non-users (cross-sectional analysis); (ii) factors associated with amantadine initiation (longitudinal analysis); (iii) amantadine effect on LIDs, MFs, apathy, impulse control disorders and freezing of gait (Fog) (longitudinal analysis).

resultsAmantadine use prevalence was 12.6% (1,585/12,542, median dose = 200 mg). Amantadine users were significantly younger, with longer and more severe PD symptoms, greater LEDD and more frequent use of device-aided/surgical treatment. Factors independently associated with amantadine initiation were younger age, longer PD duration, more frequent LIDs, MFs and FoG, higher LEDD and better cognitive function. 9 of the 658 patients on amantadine had stopped it at the following visit, after 12-18 months (1.3%). New users of amantadine presented a higher improvement in LIDs and MF compared to amantadine never users.

conclusionsAbout 12% of PD patients within the French NS-Park cohort used amantadine, mostly those with younger age and more severe PD. Amantadine initiation was associated with a subsequent reduction in LIDs and MFs.

Indexed as

AmantadineAntiparkinson AgentsParkinson DiseaseAgedCohort StudiesCross-Sectional StudiesDyskinesia, Drug-InducedFemaleFranceHumansLevodopaLongitudinal StudiesMaleMiddle AgedProspective StudiesAmantadineAntiparkinson AgentsLevodopaAmantadineMotor complicationsNS-ParkParkinson’s disease

Identifiers

PMID38578434
OpenAlexW4393983061

What OpenQuestion holds

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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.