Amantadine use in the French prospective NS-Park cohort.
Amantadine
Motor complications
NS-Park
Parkinson’s disease
Journal
Journal of neural transmission (Vienna, Austria : 1996)
ISSN: 1435-1463
Titre abrégé: J Neural Transm (Vienna)
Pays: Austria
ID NLM: 9702341
Informations de publication
Date de publication:
05 Apr 2024
05 Apr 2024
Historique:
received:
15
02
2024
accepted:
25
03
2024
medline:
5
4
2024
pubmed:
5
4
2024
entrez:
5
4
2024
Statut:
aheadofprint
Résumé
To assess amantadine use and associated factors in the patients with Parkinson's disease (PD). Immediate-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. Variables 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). Amantadine 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. About 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.
Sections du résumé
OBJECTIVE
OBJECTIVE
To assess amantadine use and associated factors in the patients with Parkinson's disease (PD).
BACKGROUND
BACKGROUND
Immediate-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.
METHODS
METHODS
Variables 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).
RESULTS
RESULTS
Amantadine 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.
CONCLUSIONS
CONCLUSIONS
About 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.
Identifiants
pubmed: 38578434
doi: 10.1007/s00702-024-02772-4
pii: 10.1007/s00702-024-02772-4
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Investigateurs
Mickael Aubignat
(M)
Eloi Magnin
(E)
Pr Pierre Burbaud
(PP)
Pr Dominique Guehl
(PD)
Alexandra Foubert-Samier
(A)
Brice Laurens
(B)
Thomas Boraud
(T)
Sylvain Vergnet
(S)
David Bendetowicz
(D)
Thomas Palpacuer
(T)
Bérengère Debilly
(B)
Philippe Derost
(P)
Charlotte Beal
(C)
Hayet Salhi
(H)
Alice Dormeuil
(A)
Aimée Petit
(A)
Alban Gravier
(A)
Gwendoline Dupont
(G)
Lucie Garnier
(L)
Valérie Fraix
(V)
Anna Castrioto
(A)
Sara Meoni
(S)
Nicolas Carriere
(N)
Teodor Danaila
(T)
Chloé Laurencin
(C)
Stéphane Thobois
(S)
Jean-Philippe Azulay
(JP)
Frédérique Fluchere
(F)
Mahmoud Charif
(M)
Marie-Christine Picot
(MC)
Lucie Hopes
(L)
Anne-Gaelle Corbille
(AG)
Tiphaine Rouaud
(T)
Pascal Derkinderen
(P)
Cosmin Alecu
(C)
Charlotte Heraud
(C)
Marie De Verdal
(M)
Bertrand Degos
(B)
Graziella Mangone
(G)
Sara Sambin
(S)
Aymeric Lanore
(A)
Thomas Courtin
(T)
Louise-Laure Mariani
(LL)
David Bendetowicz
(D)
Fouad Khoury
(F)
Poornima Menon
(P)
Florence Cormier-Dequaire
(F)
Emmanuel Flamand-Roze
(E)
David Grabli
(D)
Elodie Hainque
(E)
Marie Vidhaillet
(M)
Aurélie Meneret
(A)
Cécile Delorme
(C)
Cendrine Foucard
(C)
Florian Von Raison
(F)
Alexis Elbaz
(A)
Andreas Hartmann
(A)
Vincent Leclercq
(V)
Solène Ansquer
(S)
Frederique Leh
(F)
Marion Leclercq
(M)
Guillaume Costentin
(G)
None Lagha Boukbiza
Christine Brefel Courbon
(C)
Clemence Leung
(C)
Hélène Catala
(H)
Astrid Causel
(A)
Emilie Gaiffe
(E)
Sandrine Dupouy
(S)
Sandrine Villars
(S)
Wei-Ho Lai
(WH)
Rachida Bari
(R)
Damien Chevanne
(D)
Elodie Durand
(E)
Isabelle Rieu
(I)
Stephane Bernard
(S)
Corinne Garsault
(C)
Noel Boudjema
(N)
Pascale Grebent
(P)
Andrea Kistner
(A)
Pierre Pelissier
(P)
Valérie Santraine
(V)
Thomas Gaudin
(T)
Pierre Boutet
(P)
Catherine Caire
(C)
Manel Nouira
(M)
Claudia Verna
(C)
Amory Jardel
(A)
Salomé Puisieux
(S)
Guillemette Clement
(G)
Lili Le Monnier
(L)
Régis Frenais
(R)
Séverine Le Dily
(S)
Rachel Chaigneau
(R)
Vanessa Ferrier
(V)
Elodie David
(E)
Leslie Fra
(L)
Elsa Foucaran
(E)
Carole Dongmo-Kenfack
(C)
Florence Beauzor
(F)
Mickael Le
(M)
Sonia Messar
(S)
Sophie Liot
(S)
Emilie Rabois
(E)
Margaux Bonnaire-Verdier
(M)
Françoise Kestens
(F)
Rozenn Gourhan
(R)
Sandra Lopez-Alfaro
(S)
Jean-François Houvenaghel
(JF)
Mélanie Alexandre
(M)
Christine Bourdonnais
(C)
Linda Vernon
(L)
Ahmed Boumediene
(A)
Céline Julie
(C)
Aurette Lobstein
(A)
Nadine Longato
(N)
Marie-Pierre Mitterle
(MP)
Clélie Philips
(C)
Hugo Rummel
(H)
Stéphanie Bras
(S)
Estelle Harroch
(E)
Claudia Gillet
(C)
Informations de copyright
© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.
Références
Deuschl G, Schade-Brittinger C, Krack P, Volkmann J, Schäfer H, Bötzel K, Daniels C, Deutschländer A, Dillmann U, Eisner W, Gruber D, Hamel W, Herzog J, Hilker R, Klebe S, Kloss M, Koy J, Krause M, Kupsch A, Lorenz D, Lorenzl S, Mehdorn HM, Moringlane JR, Oertel W, Pinsker MO, Reichmann H, Reuss A, Schneider GH, Schnitzler A, Steude U, Sturm V, Timmermann L, Tronnier V, Trottenberg T, Wojtecki L, Wolf E, Poewe W, Voges J (2006) A randomized trial of deep-brain stimulation for Parkinson’s disease. N Engl J Med 355(9):896–908. https://doi.org/10.1056/NEJMoa060281
doi: 10.1056/NEJMoa060281
pubmed: 16943402
Deuschl G, Antonini A, Costa J, Śmiłowska K, Berg D, Corvol JC, Fabbrini G, Ferreira J, Foltynie T, Mir P, Schrag A, Seppi K, Taba P, Ruzicka E, Selikhova M, Henschke N, Villanueva G, Moro E (2022) European Academy of Neurology/Movement Disorder Society-European Section Guideline on the Treatment of Parkinson’s Disease: I. Invasive Therapies. Mov Disord 37(7):1360–1374. https://doi.org/10.1002/mds.29066
doi: 10.1002/mds.29066
pubmed: 35791767
Dorsey ER, Sherer T, Okun MS, Bloem BR (2018) The emerging evidence of the Parkinson Pandemic. J Parkinsons Dis 8(s1):S3-s8. https://doi.org/10.3233/jpd-181474
doi: 10.3233/jpd-181474
pubmed: 30584159
pmcid: 6311367
Elmer LW, Juncos JL, Singer C, Truong DD, Criswell SR, Parashos S, Felt L, Johnson R, Patni R (2018) Pooled Analyses of Phase III Studies of ADS-5102 (Amantadine) Extended-Release Capsules for Dyskinesia in Parkinson’s Disease. CNS Drugs 32(4):387–398. https://doi.org/10.1007/s40263-018-0498-4
doi: 10.1007/s40263-018-0498-4
pubmed: 29532440
pmcid: 5934466
Fox SH, Katzenschlager R, Lim SY, Barton B, de Bie RMA, Seppi K, Coelho M, Sampaio C (2018) International Parkinson and movement disorder society evidence-based medicine review: Update on treatments for the motor symptoms of Parkinson’s disease. Mov Disord 33(8):1248–1266. https://doi.org/10.1002/mds.27372
doi: 10.1002/mds.27372
pubmed: 29570866
Goetz CG, Poewe W, Rascol O, Sampaio C, Stebbins GT, Counsell C, Giladi N, Holloway RG, Moore CG, Wenning GK, Yahr MD, Seidl L (2004) Movement Disorder Society Task Force report on the Hoehn and Yahr staging scale: status and recommendations. Mov Disord 19(9):1020–1028. https://doi.org/10.1002/mds.20213
doi: 10.1002/mds.20213
pubmed: 15372591
Goetz CG, Tilley BC, Shaftman SR, Stebbins GT, Fahn S, Martinez-Martin P, Poewe W, Sampaio C, Stern MB, Dodel R, Dubois B, Holloway R, Jankovic J, Kulisevsky J, Lang AE, Lees A, Leurgans S, LeWitt PA, Nyenhuis D, Olanow CW, Rascol O, Schrag A, Teresi JA, van Hilten JJ, LaPelle N (2008) Movement Disorder Society-sponsored revision of the Unified Parkinson’s Disease Rating Scale (MDS-UPDRS): scale presentation and clinimetric testing results. Mov Disord 23(15):2129–2170. https://doi.org/10.1002/mds.22340
doi: 10.1002/mds.22340
pubmed: 19025984
Hauser RA, Walsh RR, Pahwa R, Chernick D, Formella AE (2021) Amantadine ER (Gocovri(®)) significantly increases ON time without any dyskinesia: pooled analyses from pivotal trials in Parkinson’s disease. Front Neurol 12:645706. https://doi.org/10.3389/fneur.2021.645706
doi: 10.3389/fneur.2021.645706
pubmed: 33841311
pmcid: 8032973
Hughes AJ, Daniel SE, Kilford L, Lees AJ (1992) Accuracy of clinical diagnosis of idiopathic Parkinson’s disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry 55(3):181–184. https://doi.org/10.1136/jnnp.55.3.181
doi: 10.1136/jnnp.55.3.181
pubmed: 1564476
pmcid: 1014720
Kaasinen V, Luo S, Martinez-Martin P, Goetz CG, Stebbins GT (2023) Cross-cultural differences in patient perceptions of dyskinesia in Parkinson’s disease. Mov Disord 38(4):688–692. https://doi.org/10.1002/mds.29335
doi: 10.1002/mds.29335
pubmed: 36670051
LeWitt PA (2015) Levodopa therapy for Parkinson’s disease: Pharmacokinetics and pharmacodynamics. Mov Disord 30(1):64–72. https://doi.org/10.1002/mds.26082
doi: 10.1002/mds.26082
pubmed: 25449210
Lim SY, Tan AH, Ahmad-Annuar A, Klein C, Tan LCS, Rosales RL, Bhidayasiri R, Wu YR, Shang HF, Evans AH, Pal PK, Hattori N, Tan CT, Jeon B, Tan EK, Lang AE (2019) Parkinson’s disease in the Western Pacific Region. Lancet Neurol 18(9):865–879. https://doi.org/10.1016/s1474-4422(19)30195-4
doi: 10.1016/s1474-4422(19)30195-4
pubmed: 31175000
Mariani LL, Doulazmi M, Chaigneau V, Brefel-Courbon C, Carrière N, Danaila T, Defebvre L, Defer G, Dellapina E, Doé de Maindreville A, Geny C, Maltête D, Meissner WG, Rascol O, Thobois S, Torny F, Tranchant C, Vidailhet M, Corvol JC, Degos B (2019) Descriptive analysis of the French NS-Park registry: towards a nation-wide Parkinson’s disease cohort? Parkinsonism Relat Disord 64:226–234. https://doi.org/10.1016/j.parkreldis.2019.04.012
doi: 10.1016/j.parkreldis.2019.04.012
pubmed: 31047798
Orayj K, Lane E (2019) Patterns and determinants of prescribing for Parkinson’s disease: a systematic literature review. Parkinson’s Dis. https://doi.org/10.1155/2019/9237181
doi: 10.1155/2019/9237181
Ory-Magne F, Corvol JC, Azulay JP, Bonnet AM, Brefel-Courbon C, Damier P, Dellapina E, Destée A, Durif F, Galitzky M, Lebouvier T, Meissner W, Thalamas C, Tison F, Salis A, Sommet A, Viallet F, Vidailhet M, Rascol O (2014) Withdrawing amantadine in dyskinetic patients with Parkinson disease: the AMANDYSK trial. Neurology 82(4):300–307. https://doi.org/10.1212/wnl.0000000000000050
doi: 10.1212/wnl.0000000000000050
pubmed: 24371304
Pringsheim T, Day GS, Smith DB, Rae-Grant A, Licking N, Armstrong MJ, de Bie RMA, Roze E, Miyasaki JM, Hauser RA, Espay AJ, Martello JP, Gurwell JA, Billinghurst L, Sullivan K, Fitts MS, Cothros N, Hall DA, Rafferty M, Hagerbrant L, Hastings T, O’Brien MD, Silsbee H, Gronseth G, Lang AE (2021) Dopaminergic therapy for motor symptoms in early parkinson disease practice guideline summary: a Report of the AAN Guideline Subcommittee. Neurology 97(20):942–957. https://doi.org/10.1212/wnl.0000000000012868
doi: 10.1212/wnl.0000000000012868
pubmed: 34782410
pmcid: 8672433
Rascol O, Negre-Pages L, Damier P, Delval A, Derkinderen P, Destée A, Fabbri M, Meissner WG, Rachdi A, Tison F, Perez-Lloret S (2020) Utilization patterns of amantadine in Parkinson’s disease patients enrolled in the French COPARK Study. Drugs Aging 37(3):215–223. https://doi.org/10.1007/s40266-019-00740-2
doi: 10.1007/s40266-019-00740-2
pubmed: 31919803
Rascol O, Fabbri M, Poewe W (2021) Amantadine in the treatment of Parkinson’s disease and other movement disorders. Lancet Neurol 20(12):1048–1056. https://doi.org/10.1016/s1474-4422(21)00249-0
doi: 10.1016/s1474-4422(21)00249-0
pubmed: 34678171
Rascol O, Ory-Magne F, Azulay JP, Defebvre L, Houeto JL, Maltete D, Remy P, Foubert-Samier A, Sommet A, Thalamas C, Thobois S, Corvol JC, Ns-Park/Fcrin N (2023) Decreased occurrence of dyskinesia when combining amantadine to L-DOPA in early parkinson disease (PD): the PREMANDYSK Trial. Mov Disord 38
Rosa MM, Ferreira JJ, Coelho M, Freire R, Sampaio C (2010) Prescribing patterns of antiparkinsonian agents in Europe. Mov Disord 25(8):1053–1060. https://doi.org/10.1002/mds.23038
doi: 10.1002/mds.23038
pubmed: 20222132
Thomas A, Bonanni L, Gambi F, Di Iorio A, Onofrj M (2010) Pathological gambling in Parkinson disease is reduced by amantadine. Ann Neurol 68(3):400–404. https://doi.org/10.1002/ana.22029
doi: 10.1002/ana.22029
pubmed: 20687121
Tomlinson CL, Stowe R, Patel S, Rick C, Gray R, Clarke CE (2010) Systematic review of levodopa dose equivalency reporting in Parkinson’s disease. Mov Disord 25(15):2649–2653. https://doi.org/10.1002/mds.23429
doi: 10.1002/mds.23429
pubmed: 21069833
Verhagen Metman L, Del Dotto P, van den Munckhof P, Fang J, Mouradian MM, Chase TN (1998) Amantadine as treatment for dyskinesias and motor fluctuations in Parkinson’s disease. Neurology 50(5):1323–1326. https://doi.org/10.1212/wnl.50.5.1323
doi: 10.1212/wnl.50.5.1323
pubmed: 9595981
Warren Olanow C, Kieburtz K, Rascol O, Poewe W, Schapira AH, Emre M, Nissinen H, Leinonen M, Stocchi F (2013) Factors predictive of the development of Levodopa-induced dyskinesia and wearing-off in Parkinson’s disease. Mov Disord 28(8):1064–1071. https://doi.org/10.1002/mds.25364
doi: 10.1002/mds.25364
pubmed: 23630119
Weintraub D, Sohr M, Potenza MN, Siderowf AD, Stacy M, Voon V, Whetteckey J, Wunderlich GR, Lang AE (2010) Amantadine use associated with impulse control disorders in Parkinson disease in cross-sectional study. Ann Neurol 68(6):963–968. https://doi.org/10.1002/ana.22164
doi: 10.1002/ana.22164
pubmed: 21154480
Zhang ZX, Chen H, Chen SD, Shao M, Sun SG, Qu QM, Zhang BR, Liu YM, Xu Q, Wan X, Li L, Wen HB, Chen X, Chen HB, Liu ZG, Wang J, Wang G (2014) Chinese culture permeation in the treatment of Parkinson disease: a cross-sectional study in four regions of China. BMC Res Notes 7:65. https://doi.org/10.1186/1756-0500-7-65
doi: 10.1186/1756-0500-7-65
pubmed: 24476129
pmcid: 3928922