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安非他酮与选择性5-羟色胺再摄取抑制剂治疗重度抑郁症焦虑症状的疗效:对10项双盲随机临床试验个体患者数据的荟萃分析

Efficacy of bupropion and the selective serotonin reuptake inhibitors in the treatment of anxiety symptoms in major depressive disorder: a meta-analysis of individual patient data from 10 double-blind, randomized clinical trials.

作者信息

Papakostas George I, Trivedi Madhukar H, Alpert Jonathan E, Seifert Cheryl A, Krishen Alok, Goodale Elizabeth P, Tucker Vivian L

机构信息

Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

J Psychiatr Res. 2008 Jan;42(2):134-40. doi: 10.1016/j.jpsychires.2007.05.012. Epub 2007 Jul 12.

Abstract

The goal of this work was to compare the efficacy of the norepinephrine-dopamine reuptake inhibitor bupropion with the selective serotonin reuptake inhibitors (SSRIs) in the treatment of anxiety symptoms in major depressive disorder (MDD). Ten double-blind, randomized studies, involving a total of 2890 bupropion-, SSRI- or placebo- treated patients were pooled. Anxiety symptoms of depression were defined using the Hamilton depression rating scale (HDRS) Anxiety-Somatization factor (HDRS-AS) score, as well as the Hamilton anxiety scale (HAM-A) score. Both bupropion and the SSRIs led to a comparable degree of improvement in anxiety symptoms, defined using the HDRS-AS score (-3.8+/-2.8 vs. -3.9+/-2.8, p=0.130) or HAM-A score (-8.8+/-7.2 vs. -9.1+/-7.0, p=0.177). There was no consistent difference in the time to anxiolysis between the two treatment groups. In addition, there was no difference in the proportion of bupropion- and SSRI- remitters who continued to experience residual anxiety, defined as a HDRS-AS score >0 at endpoint (69.2% vs. 74.7%, p=0.081) or a HAM-A score >7 at endpoint (9.5% vs. 8.4%, p=0.284). Finally, there was no statistically significant difference in the severity of residual anxiety symptoms between bupropion- or SSRI- treated patients with remitted depression, defined using the HDRS-AS (1.15+/-1.14 vs. 1.25+/-1.09, p=0.569), or HAM-A scores at endpoint (3.30+/-2.89 vs. 3.31+/-2.89, p=0.552). Contrary to clinician impression, there does not appear to be any difference in the anxiolytic efficacy of bupropion and the SSRIs when used to treat MDD.

摘要

这项研究的目的是比较去甲肾上腺素-多巴胺再摄取抑制剂安非他酮与选择性5-羟色胺再摄取抑制剂(SSRIs)治疗重度抑郁症(MDD)焦虑症状的疗效。汇总了10项双盲、随机研究,共纳入2890例接受安非他酮、SSRIs或安慰剂治疗的患者。使用汉密尔顿抑郁评定量表(HDRS)焦虑-躯体化因子(HDRS-AS)评分以及汉密尔顿焦虑量表(HAM-A)评分来定义抑郁的焦虑症状。安非他酮和SSRIs在使用HDRS-AS评分(-3.8±2.8对-3.9±2.8,p=0.130)或HAM-A评分(-8.8±7.2对-9.1±7.0,p=0.177)定义的焦虑症状改善程度上相当。两个治疗组在达到抗焦虑作用的时间上没有一致的差异。此外,在终点时仍有残留焦虑(定义为终点时HDRS-AS评分>0,69.2%对74.7%,p=0.081;或终点时HAM-A评分>7,9.5%对8.4%,p=0.284)的安非他酮和SSRIs缓解者比例没有差异。最后,在使用HDRS-AS(1.15±1.14对1.25±1.09,p=0.569)或终点时HAM-A评分(3.30±2.89对3.31±2.89,p=0.552)定义的已缓解抑郁的安非他酮或SSRIs治疗患者中,残留焦虑症状的严重程度没有统计学显著差异。与临床医生的印象相反,在用于治疗MDD时,安非他酮和SSRIs的抗焦虑疗效似乎没有任何差异。

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