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Article: Extract of Ginkgo biloba treatment for tardive dyskinesia in schizophrenia: A randomized, double-blind, placebo-controlled trial

TitleExtract of Ginkgo biloba treatment for tardive dyskinesia in schizophrenia: A randomized, double-blind, placebo-controlled trial
Authors
Issue Date2011
Citation
Journal of Clinical Psychiatry, 2011, v. 72, n. 5, p. 615-621 How to Cite?
AbstractObjective: Free radicals may be involved in the pathogenesis of tardive dyskinesia (TD). Extract of Ginkgo biloba (EGb) is a potent antioxidant possessing free radical-scavenging activities. The aim of the study was to evaluate the efficacy of EGb-761, a standardized extract given in capsule form, in treating TD in schizophrenia patients. Method: Inpatients with DSM-IV-diagnosed schizophrenia and TD (n = 157) in a mainland China Veterans Affairs psychiatric hospital were randomly assigned to 12 weeks of treatment with either EGb-761, 240 mg/d (n = 78) or a placebo (n = 79) in a double-blind manner. Primary outcome measures were (1) change from baseline in the Abnormal Involuntary Movement Scale (AIMS) score and (2) proportion of patients with a ≥ 30% reduction in their AIMS total score at week 12. Secondary outcome measures included the Positive and Negative Syndrome Scale (PANSS) and cognitive performance as measured by the Continuous Performance Test-37 Version and the 3-card Stroop task. Patients were recruited for the study between December 2006 and May 2007. Results: Of the 157 patients who were randomly assigned, 152 (96.8%) completed the study. EGb-761 treatment significantly decreased the AIMS total score in patients with TD compared to those who were given a placebo (2.13 ± 1.75 vs -0.10 ± 1.69; P < .0001), with 40 (51.3%) and 4 (5.1%) patients achieving response in the EGb-761 and placebo treatment groups, respectively. There were no between-group differences in the PANSS total score or cognitive measures from baseline to week 12. Conclusions: EGb-761 appears to be an effective treatment for reducing the symptoms of TD in schizophrenia patients, and improvement may be mediated through the well-known antioxidant activity of this extract. Trial Registration: clinicaltrials.gov identifier: NCT00672373 © Copyright 2010 Physicians Postgraduate Press, Inc.
Persistent Identifierhttp://hdl.handle.net/10722/367910
ISSN
2023 Impact Factor: 4.5
2023 SCImago Journal Rankings: 1.705

 

DC FieldValueLanguage
dc.contributor.authorZhang, Wu Fang-
dc.contributor.authorTan, Yun Long-
dc.contributor.authorZhang, Xiang Yang-
dc.contributor.authorChan, Raymond C.K.-
dc.contributor.authorWu, Hao Ran-
dc.contributor.authorZhou, Dong Feng-
dc.date.accessioned2025-12-19T08:00:17Z-
dc.date.available2025-12-19T08:00:17Z-
dc.date.issued2011-
dc.identifier.citationJournal of Clinical Psychiatry, 2011, v. 72, n. 5, p. 615-621-
dc.identifier.issn0160-6689-
dc.identifier.urihttp://hdl.handle.net/10722/367910-
dc.description.abstractObjective: Free radicals may be involved in the pathogenesis of tardive dyskinesia (TD). Extract of Ginkgo biloba (EGb) is a potent antioxidant possessing free radical-scavenging activities. The aim of the study was to evaluate the efficacy of EGb-761, a standardized extract given in capsule form, in treating TD in schizophrenia patients. Method: Inpatients with DSM-IV-diagnosed schizophrenia and TD (n = 157) in a mainland China Veterans Affairs psychiatric hospital were randomly assigned to 12 weeks of treatment with either EGb-761, 240 mg/d (n = 78) or a placebo (n = 79) in a double-blind manner. Primary outcome measures were (1) change from baseline in the Abnormal Involuntary Movement Scale (AIMS) score and (2) proportion of patients with a ≥ 30% reduction in their AIMS total score at week 12. Secondary outcome measures included the Positive and Negative Syndrome Scale (PANSS) and cognitive performance as measured by the Continuous Performance Test-37 Version and the 3-card Stroop task. Patients were recruited for the study between December 2006 and May 2007. Results: Of the 157 patients who were randomly assigned, 152 (96.8%) completed the study. EGb-761 treatment significantly decreased the AIMS total score in patients with TD compared to those who were given a placebo (2.13 ± 1.75 vs -0.10 ± 1.69; P < .0001), with 40 (51.3%) and 4 (5.1%) patients achieving response in the EGb-761 and placebo treatment groups, respectively. There were no between-group differences in the PANSS total score or cognitive measures from baseline to week 12. Conclusions: EGb-761 appears to be an effective treatment for reducing the symptoms of TD in schizophrenia patients, and improvement may be mediated through the well-known antioxidant activity of this extract. Trial Registration: clinicaltrials.gov identifier: NCT00672373 © Copyright 2010 Physicians Postgraduate Press, Inc.-
dc.languageeng-
dc.relation.ispartofJournal of Clinical Psychiatry-
dc.titleExtract of Ginkgo biloba treatment for tardive dyskinesia in schizophrenia: A randomized, double-blind, placebo-controlled trial-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.4088/JCP.09m05125yel-
dc.identifier.pmid20868638-
dc.identifier.scopuseid_2-s2.0-79959266946-
dc.identifier.volume72-
dc.identifier.issue5-
dc.identifier.spage615-
dc.identifier.epage621-

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