A randomised, double-blind, placebo-controlled trial of tropisetron in patients with schizophrenia |
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Authors: | Akihiro Shiina Yukihiko Shirayama Tomihisa Niitsu Tasuku Hashimoto Taisuke Yoshida Tadashi Hasegawa Tadashi Haraguchi Nobuhisa Kanahara Tetsuya Shiraishi Mihisa Fujisaki Goro Fukami Michiko Nakazato Masaomi Iyo Kenji Hashimoto |
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Affiliation: | 1. Department of Psychiatry, Chiba University Hospital, Chiba, Japan 2. Department of Mental Health, Teikyo University Chiba Medical Center, Chiba, Japan 3. Department of Psychiatry, Chiba University Graduate School of Medicine, Chiba, Japan 4. Division of Clinical Neuroscience, Chiba University Center for Forensic Mental Health, Chiba, Japan
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Abstract: | Background Cognitive deficits in schizophrenia are associated with psychosocial deficits that are primarily responsible for the poor long-term outcome of this disease. Auditory sensory gating P50 deficits are correlated with neuropsychological deficits in attention, one of the principal cognitive disturbances in schizophrenia. Our studies suggest that the α7 nicotinic acetylcholine receptor (α7 nAChR) agonist tropisetron might be a potential therapeutic drug for cognitive deficits in schizophrenia. Therefore, it is of particular interest to investigate the effects of tropisetron on the cognitive deficits in patients with schizophrenia. Methods A randomised, placebo-controlled trial of tropisetron in patients with schizophrenia was performed. A total of 40 patients with chronic schizophrenia who had taken risperidone (2 to 6 mg/day) were enrolled. Subjects were randomly assigned to a fixed titration of tropisetron (n = 20, 10 mg/day) or placebo (n = 20) in an 8-week double-blind trial. Auditory sensory gating P50 deficits and Quality of Life Scale (QLS), Cambridge Neuropsychological Test Automated Battery (CANTAB), and Positive and Negative Syndrome Scale (PANSS) scores were measured. Results In all, 33 patients completed the trial. Tropisetron was well tolerated. Administration of tropisetron, but not placebo, significantly improved auditory sensory gating P50 deficits in non-smoking patients with schizophrenia. The score on the rapid visual information processing (sustained visual attention) task of CANTAB was significantly improved by tropisetron treatment. Total and subscale scores of PANSS were not changed by this trial. QLS scores in the all patients, but not non-smoking patients, were significantly improved by tropisetron trial. Conclusions This first randomised, double-blind, placebo-controlled trial supports the safety and efficacy of adjunctive tropisetron for treatment of cognitive deficits in schizophrenia. |
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