Article Text

Download PDFPDF

Hypericum extract was better than placebo and equivalent to imipramine for moderate depression
Free
  1. Etienne Vermeire, MD
  1. University of Antwerp Antwerp, Belgium

    Statistics from Altmetric.com

    Request Permissions

    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

    
 
 QUESTION: In patients with moderate depression, how do the effectiveness and safety of Hypericum extract (St John's wort) compare with those of imipramine and placebo?

    Design

    8 week randomised {allocation concealed*}, blinded (clinicians and patients),* placebo controlled trial.

    Setting

    18 general practitioners' practices in Germany.

    Patients

    263 patients who were 18–65 years of age (mean age 47 y, 75% women) and had a diagnosis of moderate depression; score of ≥18 on the Hamilton Depression Rating Scale (HDRS); clinical global impression rating of moderate, marked, or severe; and depression lasting ≥4 weeks and ≤ 2 years. Exclusion criteria included bipolar disorders, alcohol or drug dependence, or suicidal risk. 230 patients (87%) completed the study; 251 (95%) were included in an intention to treat analysis.

    Intervention

    Patients were allocated to Hypericum extract (STEI 300, Steiner Arzneimittel, Berlin, Germany), 1050 mg/day (n=106); imipramine, 50 mg/day titrated to 100 mg/day by day 5 (n=110); or placebo (n=47).

    Main outcome measures

    The primary end point was change from baseline in HDRS score. Hypericum was compared with placebo at 6 weeks and with imipramine at 8 weeks.

    Main results

    At 6 weeks, greater improvement from baseline occurred with Hypericum extract than with placebo (mean decrease in HDRS score of 13.4 v 10.3, 95% CI for the 3.1 difference 1.5 to 5.4). At 8 weeks, Hypericum extract and imipramine had similar changes in score from baseline (mean decrease of 15.4 v 14.2, CI for the 1.2 difference –0.6 to 2.6). More patients who received Hypericum extract had ≥50% improvement in HDRS scores than did patients who received placebo{p=0.027}, the proportions did not differ between Hypericum and imipramine {p=0.14} (table). Fewer patients in the Hypericum group than the imipramine group reported adverse effects {p<0.001} (table).

    Hypericum extract (HE) v placebo at 6 weeks and HE v imipramine (Imi) at 8 weeks for moderate depression§

    Conclusion

    In patients with moderate depression, Hypericum extract (St John's wort) was more effective than placebo and as effective and safe as imipramine.

    Commentary

    The trial by Philipp et al suggests that Hypericum extract may be considered as a treatment for moderate depression in primary care. To determine whether to prescribe Hypericum, some issues should be addressed.

    The conclusion that Hypericum extract is safe in the long term is premature because of the limited duration of the study. Most patients are treated for many months. The fact that no data are available on concomitant pathology and drug treatments preclude statements about drug interactions. It has been shown that Hypericum induces the cytochrome P450, which might have serious clinical implications, for instance, in HIV infected patients on protease inhibitors.1 Interactions with such other drugs as cyclosporin,2 warfarin, theophylline, and some contraceptives have been reported.3 Furthermore, such common foods as grapefruit influence the same enzyme system.3 Future studies might consider using a crossover design, comparison with a selective serotonin reuptake inhibitor, or a higher dose of imipramine.

    Hypericum perforatum is an herbal remedy that, although it is widely used and has promising results in this trial, is not yet completely understood. Because Hypericum products may vary considerably in composition, prescribers should be aware that study results may not be generalised to other extracts.

    References

    Footnotes

    • Source of funding: Steiner Arzneimittel, Berlin, Germany.

    • For correspondence: Dr K O Hiller, Steiner Arzneimittel, D-12207 Berlin, Germany. Fax +49 30 712 5012.

    • Abstract also appears in Evidence-Based Mental Health.

    • * See glossary.

    • Information provided by author.

    • p Values calculated from data in article.