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用阿米替林(一种多巴胺再摄取抑制剂)治疗重性抑郁症患者。

Therapy with amineptine, a dopamine reuptake inhibitor, in patients with major depression.

机构信息

S.M. CHANNABASAVANNA, M.D., Professor of Psychiatry & Director, Department of Psychiatry, NIMHANS, Bangalore- 560029.

出版信息

Indian J Psychiatry. 1997 Apr;39(2):147-53.

Abstract

The original tricyclic antidepressant drugs are consistently underused in major depression because of side effects, delayed onset of action, and potential for overdose. In an open study of 6 weeks' duration, we studied the efficacy and acceptability of amineptine, a dopamine reuptake inhibitor, at fixed dose of 200 mg per day in 50 patients with major depression.Intention-to-treat analysis showed a patient response rate of 64% (95% CI 77-50) in HDRS, 62% (95% CI 75-48) in MADRS, 46% (95% CI 59-32) in ZUNG scale, 52% (95% CI 66-38) in Social Activity scale, and 26% ("95% CI 38-14) in CGI-severity of illness after 7 days treatment. Response in CGI-global improvement was 38% (95% CI 51-25), and in CGI-efficacy index 48% (95% CI 62-34) after 14 days of treatment. With continued therapy, only CGI-severity of illness showed a significant increase in response rate after 42 days. The treatment effect of amineptine was reflected in a significant and progressive improvement in all depression, social activity, and CGI rating scale scores throughout the study period. Somatic symptoms and side effects assessed by AMDP-5 showed significant improvement at each assessment.The clinically useful response in depression which occurred by the first week of treatment, favourable side effect profile, and the convenience of a fixed dose could make amineptine a suitable first line alternative for the treatment of major depression.

摘要

在重度抑郁症的治疗中,由于副作用、起效时间延迟和潜在的药物过量风险,传统三环类抗抑郁药的应用一直受到限制。我们进行了一项为期 6 周的开放性研究,对 50 例重度抑郁症患者采用固定剂量 200mg/天的阿米替林(一种多巴胺再摄取抑制剂)进行疗效和可接受性评估。意向治疗分析显示,在汉密尔顿抑郁量表(HDRS)、蒙哥马利-爱丁堡抑郁量表(MADRS)、zung 量表、社会活动量表和临床总体印象严重程度量表(CGI-severity of illness)上,患者的应答率分别为 64%(95%可信区间 77-50)、62%(95%可信区间 75-48)、46%(95%可信区间 59-32)、52%(95%可信区间 66-38)和 26%(95%可信区间 38-14),治疗 7 天后。CGI-global improvement 的应答率为 38%(95%可信区间 51-25),CGI-efficacy index 的应答率为 48%(95%可信区间 62-34),治疗 14 天后。继续治疗,仅在治疗第 42 天 CGI-severity of illness 的应答率有显著增加。阿米替林的治疗效果体现在整个研究期间所有抑郁、社会活动和 CGI 评分量表评分的显著且逐渐改善。通过 AMDP-5 评估的躯体症状和副作用在每次评估时均有显著改善。

阿米替林在治疗的第 1 周就出现了有临床意义的抑郁缓解,且具有良好的副作用特征,固定剂量也很方便,这使其成为治疗重度抑郁症的一线替代药物。

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