Ritsner Michael S, Gibel Anatoly, Ratner Yael, Tsinovoy German, Strous Rael D
Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
J Clin Psychopharmacol. 2006 Oct;26(5):495-9. doi: 10.1097/01.jcp.0000237942.50270.35.
Dehydroepiandrosterone (DHEA) augmentation has been reported, in a preliminary fashion, to be useful in the management of schizophrenia symptoms and side effects. In this study, the intention was to investigate the efficacy and safety of DHEA administration to ongoing antipsychotic medication in a multicenter, 12-week, double-blind, randomized, placebo-controlled, crossover trial.
Fifty-five of 62 inpatients and outpatients with Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, diagnosis of schizophrenia completed the trial. Patients were randomly allocated to 2 treatment groups receiving either DHEA (200 mg/d) or placebo for 6 weeks with the crossover between DHEA and placebo occurring after 6 weeks. Patients continued to receive their regular antipsychotic medication for the duration of the study.
Compared with placebo, DHEA administration did not produce significant improvement in clinical symptoms, side effects, and quality-of-life scores. However, 6 weeks of DHEA administration (but not placebo) was associated with a significant improvement in Positive and Negative Symptom Scale ratings compared with baseline. Furthermore, 6 weeks of DHEA treatment was associated with significant improvement in cognitive functions of visual sustained attention and visual and movement skills compared with placebo conditions. The DHEA augmentation was associated with elevations of serum concentrations of both DHEA and its sulfate ester. The DHEA treatment was well tolerated without any serious adverse effects.
This short-term study does not support DHEA's value as an effective adjunct in the treatment of symptoms, side effects, and quality-of-life impairment in schizophrenia, while suggesting that DHEA improves sustained attention and visual and movement skills. A long-term, large-scale study with a broader dose range is warranted to further investigate DHEA's role in the management of schizophrenia.
已有初步报道称,脱氢表雄酮(DHEA)补充疗法在精神分裂症症状及副作用的管理方面可能有用。本研究旨在通过一项多中心、为期12周的双盲、随机、安慰剂对照、交叉试验,探究在持续使用抗精神病药物治疗的同时给予DHEA的疗效和安全性。
62例符合《精神障碍诊断与统计手册》第四版精神分裂症诊断标准的住院及门诊患者中,有55例完成了试验。患者被随机分为2个治疗组,分别接受DHEA(200mg/d)或安慰剂治疗6周,6周后DHEA组与安慰剂组交叉。在研究期间,患者继续服用其常规抗精神病药物。
与安慰剂相比,给予DHEA并未使临床症状、副作用及生活质量评分有显著改善。然而,与基线相比,给予DHEA6周(而非安慰剂)与阳性和阴性症状量表评分的显著改善相关。此外,与安慰剂组相比,DHEA治疗6周与视觉持续注意力以及视觉和运动技能的认知功能显著改善相关。DHEA补充疗法与DHEA及其硫酸酯的血清浓度升高相关。DHEA治疗耐受性良好,未出现任何严重不良反应。
这项短期研究不支持DHEA作为治疗精神分裂症症状、副作用及生活质量损害的有效辅助药物的价值,同时表明DHEA可改善持续注意力以及视觉和运动技能。有必要进行一项长期、大规模且剂量范围更广的研究,以进一步探究DHEA在精神分裂症管理中的作用。