Intensive Rehabilitation Treatment in Early Parkinson’s Disease

Author:

Frazzitta Giuseppe12,Maestri Roberto3,Bertotti Gabriella3,Riboldazzi Giulio4,Boveri Natalia3,Perini Michele5,Uccellini Davide6,Turla Marinella7,Comi Cristoforo8,Pezzoli Gianni9,Ghilardi M. Felice10

Affiliation:

1. “Moriggia-Pelascini” Hospital, Gravedona ed Uniti, Italy

2. Fondazione Europea Ricerca Biomedica FERB, “S. Isidoro” Hospital, Trescore Balneario, Italy

3. Scientific Institute of Montescano, S. Maugeri Foundation IRCCS, Montescano, Italy

4. Macchi Foundation, Varese and Department of Rehabilitation, “Le Terrazze” Hospital, Cunardo, Italy

5. Gallarate Hospital, Gallarate, Italy

6. Tradate Hospital, Tradate, Italy

7. Valle Camonica Hospital, Esine, Italy

8. University of the Eastern Piedmont, Novara, Italy

9. Parkinson Institute, Istituti Clinici di Perfezionamento, Milan, Italy

10. City University of New York Medical School, New York, NY, USA

Abstract

Background. Although physical exercise improves motor aspects of Parkinson’s disease (PD), it is not clear whether it may also have a neuroprotective effect. Objective. In this 2-year follow-up study, we determined whether intensive exercise in the early stages of the disease slows down PD progression. Methods. Forty newly diagnosed patients with PD were treated with rasagiline and randomly assigned to 2 groups: MIRT Group (two 28-day multidisciplinary intensive rehabilitation treatments [MIRT], at 1-year interval) and Control Group (only drug). In both groups, Unified Parkinson’s Disease Rating Scale Section II (UPDRS II), UPDRS III, 6-minute walking test (6MWT), Timed Up-and-Go test (TUG); PD Disability Scale (PDDS), and l-dopa equivalents were assessed at baseline (T0), 6 months (T1), 1 year (T2), 18 months (T3), and 2 years (T4) later. Results. Over 2 years, UPDRS II, UPDRS III, TUG, and PDDS differentially progressed in the 2 groups: In the MIRT Group, all scores at T4 were better than at T0 (all Ps < .03). No changes were noted in the Control Group. l-dopa equivalent dosages increased significantly only in the Control Group ( P = .0015), with a decrease in the percentages of patients in monotherapy (T1 40%; T2, T3, and T4 20%). In the MIRT Group, the percentages of such patients remained higher (T1 and T2 100%; T3 89%; T4 75%). Conclusions. These results suggest that MIRT might slow down the progression of motor decay, it might delay the need for increasing drug treatment, and thus, it might have a neuroprotective effect.

Publisher

SAGE Publications

Subject

General Medicine

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