Mallinckrodt Craig H., Goldstein David J., Detke Michael J., Lu Yili, Watkin John G., Tran Pierre V.
Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Ind.; PRN Consulting, Indianapolis, Ind.; the Department of Pharmacology and Toxicology and the Department of Psychiatry, Indiana University School of Medicine, Indianapolis; the Department of Psychiatry, McLean Hospital, Belmont, Mass.; the Department of Psychiatry, Harvard Medical School, Boston, Mass.; and the Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, N.C.
Prim Care Companion J Clin Psychiatry. 2003 Feb;5(1):19-28. doi: 10.4088/pcc.v05n0105.
Depression is underdiagnosed in the primary care setting. Physical symptoms such as aches, pains, and gastrointestinal disturbance are frequently associated with major depressive disorder (MDD) and are often the presenting symptoms. Duloxetine, a dual-reuptake inhibitor of serotonin and norepinephrine, may have a positive effect on physical symptoms in addition to efficacy in treating emotional symptoms of depression. METHOD: Efficacy was evaluated in 6 double-blind, placebo- and/or active comparator-controlled trials of duloxetine for patients with MDD (DSM-IV criteria). Efficacy in depression was determined primarily using the 17-item Hamilton Rating Scale for Depression (HAM-D-17). Secondary efficacy measures included subscales of the HAM-D-17 and assessment of physical symptoms. Safety evaluations included adverse events, vital signs, laboratory analyses, and electrocardiograms. Safety was evaluated by pooling the data from the MDD trials and a study of duloxetine in nondepressed patients. RESULTS: Duloxetine demonstrated significant differences from placebo on core mood symptoms, physical symptoms (e.g., back pain), and global functioning as early as week 1 of treatment. The estimated probabilities of remission in the studies that demonstrated efficacy ranged from 43% to 57%. The most frequently observed adverse events for duloxetine-treated patients included nausea, dizziness, insomnia, fatigue, and somnolence. Duloxetine did not prolong corrected QT intervals, and the rate of sustained elevations of blood pressure did not differ significantly from placebo. CONCLUSION: In these studies, duloxetine was safe and effective in the treatment of both emotional and physical symptoms of MDD. Based on dose assessments, 60 mg q.d. appears to be the optimum starting and therapeutic dose.
在初级保健环境中,抑郁症的诊断不足。诸如疼痛和胃肠道不适等躯体症状常与重度抑郁症(MDD)相关,且往往是首发症状。度洛西汀是一种5-羟色胺和去甲肾上腺素双重再摄取抑制剂,除了对抑郁症的情绪症状有效外,可能对躯体症状也有积极作用。方法:在6项针对MDD患者(符合《精神疾病诊断与统计手册》第四版标准)的度洛西汀双盲、安慰剂和/或活性对照试验中评估疗效。抑郁症的疗效主要使用17项汉密尔顿抑郁量表(HAM-D-17)来确定。次要疗效指标包括HAM-D-17的分量表和躯体症状评估。安全性评估包括不良事件、生命体征、实验室分析和心电图。通过汇总MDD试验和度洛西汀在非抑郁症患者中的一项研究数据来评估安全性。结果:早在治疗第1周,度洛西汀在核心情绪症状、躯体症状(如背痛)和整体功能方面与安慰剂相比就显示出显著差异。显示有效作用的研究中,缓解的估计概率在43%至57%之间。度洛西汀治疗患者最常观察到的不良事件包括恶心、头晕、失眠、疲劳和嗜睡。度洛西汀未延长校正QT间期,血压持续升高的发生率与安慰剂相比无显著差异。结论:在这些研究中,度洛西汀在治疗MDD的情绪和躯体症状方面安全有效。根据剂量评估,每日60毫克似乎是最佳起始和治疗剂量。