Oral Zinc Sulphate Supplementation for Six Months in SCA2 Patients: A Randomized, Double-Blind, Placebo-Controlled Trial

Cuban patients with Spinocerebellar Ataxia type 2 (SCA2) have reduced concentrations of zinc in serum and cerebrospinal fluid (CSF). To assess the effect and safety of zinc supplementation, 36 Cuban SCA2 patients were randomly assigned to receive daily either 50 mg ZnSO 4 or placebo, together with n...

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Veröffentlicht in:Neurochemical research 2011-10, Vol.36 (10), p.1793-1800
Hauptverfasser: Velázquez-Pérez, Luis, Rodríguez-Chanfrau, Jorge, García-Rodríguez, Julio Cesar, Sánchez-Cruz, Gilberto, Aguilera-Rodríguez, Raúl, Rodríguez-Labrada, Roberto, Rodríguez-Díaz, Julio Cesar, Canales-Ochoa, Nalia, Gotay, Dennis Almaguer, Almaguer Mederos, Luis E., Laffita Mesa, José M., Porto-Verdecia, Marlene, Triana, Consuelo González, Pupo, Noemí Rodríguez, Batista, Idania Hidalgo, López-Hernandez, Orestes D., Polanco, Iverlis Díaz, Novas, Arelis Jayme
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Sprache:eng
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Zusammenfassung:Cuban patients with Spinocerebellar Ataxia type 2 (SCA2) have reduced concentrations of zinc in serum and cerebrospinal fluid (CSF). To assess the effect and safety of zinc supplementation, 36 Cuban SCA2 patients were randomly assigned to receive daily either 50 mg ZnSO 4 or placebo, together with neurorehabilitation therapy in a randomized, double-blind, placebo-controlled clinical trial during 6 months. Outcome measures included the changes of zinc levels in CSF and serum, ataxia score, oxidative stress and saccadic eye movements. At the end of the study, the Zinc-treated group showed: (i) a significant increase of the Zn levels in the CSF, (ii) mild decrease in the ataxia scale subscores for gait, posture, stance and dysdiadochocinesia (iii) reduction of lipid’s oxidative damage, and (iv) reduction of saccadic latency when compared with the placebo group. The treatment was safe and well tolerated by all subjects. This study demonstrated the efficacy and safety of Zn supplementation, combined with neurorehabilitation for SCA2 patients and therefore it may encourage further studies on the clinical effect of zinc supplementation in SCA2 based in the conduction of future clinical trials with higher number of subjects.
ISSN:0364-3190
1573-6903
DOI:10.1007/s11064-011-0496-0