Maher Alicia Ruelaz, Hempel Susanne, Apaydin Eric, Shanman Roberta M, Booth Marika, Miles Jeremy N V, Sorbero Melony E
Rand Health Q. 2016 May 9;5(4):12.
RAND researchers conducted a systematic review that synthesized evidence from randomized controlled trials of St. John's wort (SJW)-used adjunctively or as monotherapy-to provide estimates of its efficacy and safety in treating adults with major depressive disorder. Outcomes of interest included changes in depressive symptomatology, quality of life, and adverse effects. Efficacy meta-analyses used the Hartung-Knapp-Sidik-Jonkman method for random-effects models. Quality of evidence was assessed using the Grades of Recommendation, Assessment, Development, and Evaluation (GRADE) approach. In total, 35 studies met inclusion criteria. There is moderate evidence, due to unexplained heterogeneity between studies, that depression improvement based on the number of treatment responders and depression scale scores favors SJW over placebo, and results are comparable to antidepressants. The existing evidence is based on studies testing SJW as monotherapy; there is a lack of evidence for SJW given as adjunct therapy to standard antidepressant therapy. We found no systematic difference between SJW extracts, but head-to-head trials are missing; LI 160 (0.3% hypericin, 1-4% hyperforin) was the extract with the greatest number of studies. Only two trials assessed quality of life. SJW adverse events reported in included trials were comparable to placebo, and were fewer compared with antidepressant medication; however, adverse event assessments were limited, and thus we have limited confidence in this conclusion.
兰德公司的研究人员进行了一项系统综述,综合了来自圣约翰草(SJW)作为辅助治疗或单一疗法的随机对照试验的证据,以评估其在治疗成人重度抑郁症方面的疗效和安全性。感兴趣的结果包括抑郁症状的变化、生活质量和不良反应。疗效荟萃分析采用Hartung-Knapp-Sidik-Jonkman方法进行随机效应模型分析。使用推荐分级、评估、制定与评价(GRADE)方法评估证据质量。共有35项研究符合纳入标准。由于研究之间存在无法解释的异质性,有中等证据表明,基于治疗反应者数量和抑郁量表评分的抑郁改善情况,圣约翰草优于安慰剂,且结果与抗抑郁药相当。现有证据基于将圣约翰草作为单一疗法的研究;缺乏圣约翰草作为标准抗抑郁疗法辅助治疗的证据。我们发现圣约翰草提取物之间没有系统性差异,但缺乏直接对比试验;LI 160(0.3%金丝桃素,1 - 4%贯叶连翘提取物)是研究数量最多的提取物。只有两项试验评估了生活质量。纳入试验中报告的圣约翰草不良事件与安慰剂相当,且与抗抑郁药物相比更少;然而,不良事件评估有限,因此我们对这一结论的信心有限。