Department of Psychiatry and Behavioral Neurosciences, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
J Psychiatr Res. 2011 Jul;45(7):931-41. doi: 10.1016/j.jpsychires.2011.05.001. Epub 2011 May 31.
This paper presents new data addressing two important controversies in psychiatry: the construct of Minor Depression (MinD) and the efficacy of St. John's Wort for milder forms of depressive disorders. Data are from a three-arm, 12 week, randomized clinical trial of investigating the efficacy of St. John's Wort (810 mg/day), citalopram (20 mg/day), or placebo for acute treatment of MinD. Due to a high placebo response on all outcome measures, neither St. John's Wort nor citalopram separated from placebo on change in depressive symptom severity, quality of life, or well-being. However, systematic assessment of potential adverse effects (AEs) led to three important observations: (1) prior to the administration of study compound, 60% of subjects endorsed items that would be characterized as AEs once study compound was administered, (2) St. John's Wort and citalopram were each associated with a significant number of new or worsening AEs during treatment, and (3) using a structured interview for identifying AEs at baseline and during treatment is informative. MinD was not responsive to either a conventional antidepressant or a nutraceutical, and both compounds were associated with a notable side effects burden. Other treatment approaches for MinD should be investigated.
本文提供了新的数据,旨在解决精神病学中的两个重要争议:轻度抑郁症(MinD)的构建和圣约翰草治疗轻度抑郁障碍的疗效。数据来自一项为期 12 周的三臂随机临床试验,旨在研究圣约翰草(810mg/天)、西酞普兰(20mg/天)或安慰剂治疗 MinD 的急性疗效。由于所有结局指标的安慰剂反应都很高,圣约翰草或西酞普兰在抑郁症状严重程度、生活质量或幸福感的改善方面均未与安慰剂分离。然而,对潜在不良反应(AE)的系统评估得出了三个重要观察结果:(1)在给予研究化合物之前,60%的受试者对在给予研究化合物后会被归类为 AE 的项目表示赞同;(2)圣约翰草和西酞普兰在治疗期间都与相当数量的新的或恶化的 AE 相关;(3)使用结构化访谈来识别基线和治疗期间的 AE 是有信息性的。MinD 对传统抗抑郁药或营养保健品均无反应,并且这两种药物都与显著的副作用负担相关。应研究其他治疗 MinD 的方法。