Driesens F
Janssen Pharmaceutica, Beerse, Belgium.
Acta Psychiatr Belg. 1988 May-Jun;88(3):195-205.
The literature concerning the connection between Tardive Dyskinesia (TD) and the chronic use of neuroleptics is reviewed. On the average, three times more TD's can be observed in a population treated chronically with neuroleptics (about 20%) than in untreated groups (5-9%). Various analyses do not justify the contention that one neuroleptic or group of neuroleptics would elicit more TD's than another one. Questions about the mechanisms by which TD is brought about remain unanswered. More attention is now being paid to brain function and age. Possible changes in the sensitivity of the dopamine receptor are no longer being regarded as a primary mechanism. A working hypothesis is proposed according to which TD would be induced by various adaptation mechanisms in the brain, which also points to a possible explanation of the reversibility of TD. It is now accepted that TD symptoms can disappear or improve greatly in about 60% of patients during the course of 2-3 years, which reduces the group of irreversible TD's to the number of spontaneously occurring dyskinesias.
本文回顾了有关迟发性运动障碍(TD)与长期使用抗精神病药物之间联系的文献。平均而言,长期接受抗精神病药物治疗的人群中观察到的TD病例数(约20%)是未治疗组(5 - 9%)的三倍。各种分析并不支持某一种抗精神病药物或一组抗精神病药物比另一种更容易引发TD的观点。关于TD产生的机制问题仍未得到解答。目前人们更多地关注脑功能和年龄。多巴胺受体敏感性的可能变化不再被视为主要机制。提出了一个工作假说,即TD是由大脑中的各种适应性机制诱发的,这也为TD的可逆性提供了一种可能的解释。现在人们已经认识到,约60%的患者在2 - 3年的病程中TD症状可消失或显著改善,这使得不可逆TD的数量减少到与自发性运动障碍相当的水平。