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Trial of Deferiprone in Parkinson's Disease

Authors :
Devos, D.
Labreuche, J.
Rascol, O.
Corvol, J.C.
Duhamel, A.
Delannoy, P. Guyon
Poewe, W.
Compta, Y.
Pavese, N.
Růžička, E.
Dušek, P.
Post, B.
Bloem, B.R.
Berg, D.
Maetzler, W.
Otto, M.
Habert, M.O.
Lehericy, S.
Ferreira, J.
Dodel, R.
Tranchant, C.
Eusebio, A.
Thobois, S.
Marques, A.R.
Meissner, W.G.
Ory-Magne, F.
Walter, U.
Bie, R.M. de
Gago, M.
Vilas, D.
Kulisevsky, J.
Januario, C.
Coelho, M.V.S.
Behnke, S.
Worth, P.
Seppi, K.
Ouk, T.
Potey, C.
Leclercq, C.
Viard, R.
Kuchcinski, G.
Lopes, R.
Pruvo, J.P.
Pigny, P.
Garçon, G.
Simonin, O.
Carpentier, J.
Rolland, A.S.
Nyholm, D.
Scherfler, C.
Mangin, J.F.
Chupin, M.
Bordet, R.
Dexter, D.T.
Fradette, C.
Spino, M.
Tricta, F.
Ayton, S.
Bush, A.I.
Devedjian, J.C.
Duce, J.A.
Cabantchik, I.
Defebvre, L.
Deplanque, D.
Moreau, C.
Devos, D.
Labreuche, J.
Rascol, O.
Corvol, J.C.
Duhamel, A.
Delannoy, P. Guyon
Poewe, W.
Compta, Y.
Pavese, N.
Růžička, E.
Dušek, P.
Post, B.
Bloem, B.R.
Berg, D.
Maetzler, W.
Otto, M.
Habert, M.O.
Lehericy, S.
Ferreira, J.
Dodel, R.
Tranchant, C.
Eusebio, A.
Thobois, S.
Marques, A.R.
Meissner, W.G.
Ory-Magne, F.
Walter, U.
Bie, R.M. de
Gago, M.
Vilas, D.
Kulisevsky, J.
Januario, C.
Coelho, M.V.S.
Behnke, S.
Worth, P.
Seppi, K.
Ouk, T.
Potey, C.
Leclercq, C.
Viard, R.
Kuchcinski, G.
Lopes, R.
Pruvo, J.P.
Pigny, P.
Garçon, G.
Simonin, O.
Carpentier, J.
Rolland, A.S.
Nyholm, D.
Scherfler, C.
Mangin, J.F.
Chupin, M.
Bordet, R.
Dexter, D.T.
Fradette, C.
Spino, M.
Tricta, F.
Ayton, S.
Bush, A.I.
Devedjian, J.C.
Duce, J.A.
Cabantchik, I.
Defebvre, L.
Deplanque, D.
Moreau, C.
Source :
The New England Journal of Medicine; 2045; 2055; 0028-4793; 22; 387; ~The New England Journal of Medicine~2045~2055~~~0028-4793~22~387~~
Publication Year :
2022

Abstract

Item does not contain fulltext<br />BACKGROUND: Iron content is increased in the substantia nigra of persons with Parkinson's disease and may contribute to the pathophysiology of the disorder. Early research suggests that the iron chelator deferiprone can reduce nigrostriatal iron content in persons with Parkinson's disease, but its effects on disease progression are unclear. METHODS: We conducted a multicenter, phase 2, randomized, double-blind trial involving participants with newly diagnosed Parkinson's disease who had never received levodopa. Participants were assigned (in a 1:1 ratio) to receive oral deferiprone at a dose of 15 mg per kilogram of body weight twice daily or matched placebo for 36 weeks. Dopaminergic therapy was withheld unless deemed necessary for symptom control. The primary outcome was the change in the total score on the Movement Disorder Society-sponsored revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS; range, 0 to 260, with higher scores indicating more severe impairment) at 36 weeks. Secondary and exploratory clinical outcomes at up to 40 weeks included measures of motor and nonmotor disability. Brain iron content measured with the use of magnetic resonance imaging was also an exploratory outcome. RESULTS: A total of 372 participants were enrolled; 186 were assigned to receive deferiprone and 186 to receive placebo. Progression of symptoms led to the initiation of dopaminergic therapy in 22.0% of the participants in the deferiprone group and 2.7% of those in the placebo group. The mean MDS-UPDRS total score at baseline was 34.3 in the deferiprone group and 33.2 in the placebo group and increased (worsened) by 15.6 points and 6.3 points, respectively (difference, 9.3 points; 95% confidence interval, 6.3 to 12.2; P<0.001). Nigrostriatal iron content decreased more in the deferiprone group than in the placebo group. The main serious adverse events with deferiprone were agranulocytosis in 2 participants and neutropenia in 3 participants. CONCLUSIONS: In parti

Details

Database :
OAIster
Journal :
The New England Journal of Medicine; 2045; 2055; 0028-4793; 22; 387; ~The New England Journal of Medicine~2045~2055~~~0028-4793~22~387~~
Publication Type :
Electronic Resource
Accession number :
edsoai.on1367191460
Document Type :
Electronic Resource