Melatonin treatment for tardive dyskinesia - A double-blind, placebo-controlled, crossover study

被引:115
|
作者
Shamir, E
Barak, Y
Shalman, I
Laudon, M
Zisapel, N
Tarrasch, R
Elizur, A
Weizman, R
机构
[1] Abarbanel Mental Hlth Ctr, IL-59100 Bat Yam, Israel
[2] Tel Aviv Univ, Neurim Pharmaceut Ltd, Sackler Fac Med, Tel Aviv, Israel
[3] Tel Aviv Univ, Neurim Pharmaceut Ltd, Fac Life Sci, Dept Neurobiochem, Tel Aviv, Israel
[4] Tel Aviv Univ, Neurim Pharmaceut Ltd, Dept Psychol, Tel Aviv, Israel
[5] Tel Aviv Mental Hlth Ctr, Tel Aviv, Israel
关键词
D O I
10.1001/archpsyc.58.11.1049
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Antipsychotics remain the mainstay of drug intervention in the management of schizophrenia. However, long-term treatment with antipsychotics is associated with a variety of movement disorders, the most disabling of which is tardive dyskinesia (TD), which occurs in up to 50% of patients hospitalized with chronic schizophrenia. The pathophysiology of TD is still unclear and no definite treatment exists. Both dopamine receptor supersensitivity and oxidative stress-induced neurotoxicity in the nigrostriatal system are apparently implicated. The pineal hormone melatonin is a potent antioxidant and attenuates dopaminergic activity in the striatum and dopamine release from the hypothalamus. Thus, it may have a beneficial effect for both the treatment and prevention of TD. crossover study, we evaluated the efficacy of 10 mg/d of melatonin for 6 weeks in 22 patients with schizophrenia and TD. The primary outcome measure was the change from baseline in Abnormal Involuntary Movement Scale (AIMS) score. Results: The decrease (mean SD) in AIMS score was 2.45 +/- 1.92 for the melatonin and 0.77 +/- 1.11 for the placebo treatment groups (P < .001). No adverse events or side effects were noted. Conclusion: This is the first clinical evidence for efficacy of melatonin in the treatment of TD. Methods: Using a double-blind, placebo-controlled,
引用
收藏
页码:1049 / 1052
页数:4
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