TY - JOUR
T1 - Effects of zonisamide on tardive dyskinesia
T2 - A preliminary open-label trial
AU - Iwata, Yusuke
AU - Irie, Sachiko
AU - Uchida, Hiroyuki
AU - Suzuki, Takefumi
AU - Watanabe, Koichiro
AU - Iwashita, Satoru
AU - Mimura, Masaru
N1 - Funding Information:
Dr. Uchida has received grants, speaker's honoraria, or manuscript fees from Pfizer Health Research Foundation, GlaxoSmithKline, Otsuka Pharmaceutical, Dainippon Sumitomo Pharma, Janssen Pharmaceutical, and Pfizer within the past 5 years. Dr. Suzuki has received fellowship grants from the Japanese Society of Clinical Psychopharmacology, Government of Canada Post-Doctoral Research Fellowships, Foundation and Mochida Memorial Foundation, and manuscript fees from Dainippon Sumitomo Pharma and Kyowa Hakko Kirin, and speakers' honoraria from Eli Lilly within the past 5 years. Dr. Mimura has received grants, or consultant fees from Eisai, Astellas Pharma, GlaxoSmithKline and Meiji, and received speaker's honoraria from Astellas Pharma, Dainippon Sumitomo Pharma, Eli Lilly, GlaxoSmithKline, Janssen Pharmaceutical, Meiji, Otsuka Pharmaceutical, Pfizer, and Yoshitomiyakuhin within the past 5 years.
Copyright:
Copyright 2013 Elsevier B.V., All rights reserved.
PY - 2012/4/15
Y1 - 2012/4/15
N2 - Once developed, tardive dyskinesia (TD) is a challenging condition to treat. The recent evidence has indicated that zonisamide, an antiepileptic drug indicated for partial-onset seizures, may also have beneficial effects for ameliorating dyskinesia in Parkinson's disease. However, this finding has not systematically been tested in psychiatric patients with TD associated with antipsychotic treatment. The objective of this study was to examine the efficacy, tolerability, and safety of zonisamide against TD in these patients. In this 4-week open-label study, subjects who suffered TD were given 50-100 mg/day of add-on zonisamide. Severity of TD was evaluated at the baseline and endpoint, using the Abnormal Involuntary Movement Scale (AIMS). Eleven subjects (6 females; mean ± SD age, 75.5 ± 4.7 years; schizophrenia [N = 6], bipolar affective disorder [N = 2], schizoaffective disorder [N = 1], mental retardation [N = 1], mental retardation with epilepsy [N = 1]; 6 were antipsychotic free at baseline) participated in this study. The AIMS total score (mean ± SD) was significantly decreased from 24.1 ± 5.5 to 19.5 ± 5.9, with 36.4% of the subjects (N = 4) demonstrating 20% or more decrease in the AIMS total score. Treatment with zonisamide was well-tolerated and no participants dropped out prematurely. In conclusion, zonisamide may be safe and effective for the treatment of TD associated with antipsychotic treatment. These preliminary findings need to be further explored by larger well-designed trials.
AB - Once developed, tardive dyskinesia (TD) is a challenging condition to treat. The recent evidence has indicated that zonisamide, an antiepileptic drug indicated for partial-onset seizures, may also have beneficial effects for ameliorating dyskinesia in Parkinson's disease. However, this finding has not systematically been tested in psychiatric patients with TD associated with antipsychotic treatment. The objective of this study was to examine the efficacy, tolerability, and safety of zonisamide against TD in these patients. In this 4-week open-label study, subjects who suffered TD were given 50-100 mg/day of add-on zonisamide. Severity of TD was evaluated at the baseline and endpoint, using the Abnormal Involuntary Movement Scale (AIMS). Eleven subjects (6 females; mean ± SD age, 75.5 ± 4.7 years; schizophrenia [N = 6], bipolar affective disorder [N = 2], schizoaffective disorder [N = 1], mental retardation [N = 1], mental retardation with epilepsy [N = 1]; 6 were antipsychotic free at baseline) participated in this study. The AIMS total score (mean ± SD) was significantly decreased from 24.1 ± 5.5 to 19.5 ± 5.9, with 36.4% of the subjects (N = 4) demonstrating 20% or more decrease in the AIMS total score. Treatment with zonisamide was well-tolerated and no participants dropped out prematurely. In conclusion, zonisamide may be safe and effective for the treatment of TD associated with antipsychotic treatment. These preliminary findings need to be further explored by larger well-designed trials.
KW - Antiepileptic drug
KW - Free radicals
KW - Parkinsonism
KW - Tardive dyskinesia
KW - Treatment
KW - Zonisamide
UR - http://www.scopus.com/inward/record.url?scp=84862779333&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84862779333&partnerID=8YFLogxK
U2 - 10.1016/j.jns.2011.12.010
DO - 10.1016/j.jns.2011.12.010
M3 - Article
C2 - 22285275
AN - SCOPUS:84862779333
SN - 0022-510X
VL - 315
SP - 137
EP - 140
JO - Journal of the Neurological Sciences
JF - Journal of the Neurological Sciences
IS - 1-2
ER -