Inada T, Yagi G
National Institute of Mental Health, National Center of Neurology and Psychiatry, Chiba, Japan.
Psychiatry Clin Neurosci. 1995 Dec;49(5-6):239-44. doi: 10.1111/j.1440-1819.1995.tb01895.x.
This article reviews current topics in tardive dyskinesia (TD), a movement disorder associated with the prolonged use of neuroleptic agents, especially therapeutic and preventive strategies which have been or are now being studied in Japan. Tardive dyskinesia has become a major problem in the clinical psychiatric field since the early 1970s in Japan, lagging behind Western countries by more than 10 years. The average prevalence rate of TD has been estimated as 7.7% in Japan, while it has been reported in the English literature at around 15 to 20%. Clinical trials of treatments for TD have been or are now being performed in Japan with a number of novel compounds, such as ceruletide, meclofenoxate, and rolipram; however, no effective treatment has yet been established and measures to prevent TD have therefore been emphasized. These include (i) the development of new antipsychotic drugs which are free from TD, (ii) the identification of risk factors from prospective longitudinal studies, and (iii) the investigation of genetic variations that could act as a marker to identify especially vulnerable patients within the whole population of patients who need neuroleptic therapy.
本文综述了迟发性运动障碍(TD)的当前研究课题,TD是一种与长期使用抗精神病药物相关的运动障碍,尤其关注在日本已经或正在研究的治疗和预防策略。自20世纪70年代初以来,迟发性运动障碍在日本临床精神病学领域已成为一个主要问题,比西方国家落后了10多年。据估计,日本TD的平均患病率为7.7%,而英文文献报道的患病率约为15%至20%。日本已经或正在对多种新型化合物,如蛙皮素、氯酯醒和咯利普兰,进行TD治疗的临床试验;然而,尚未确立有效的治疗方法,因此预防TD的措施受到了重视。这些措施包括:(i)开发无TD的新型抗精神病药物;(ii)通过前瞻性纵向研究确定风险因素;(iii)研究基因变异,这些变异可作为一种标志物,用于在需要抗精神病治疗的患者总体中识别特别易患TD的患者。