Duloxetine Efficacy for Major Depressive Disorder in Male vs. Female Patients

度洛西汀 安慰剂 重性抑郁障碍 临床全球印象 汉密尔顿焦虑量表 盐酸度洛西汀 汉密尔顿抑郁量表 焦虑 萧条(经济学) 心理学 内科学 评定量表 可视模拟标度 精神科 抗抑郁药 医学 广泛性焦虑症 物理疗法 心情 发展心理学 替代医学 病理 经济 宏观经济学
作者
Susan G. Kornstein,Madelaine M. Wohlreich,Craig Mallinckrodt,John G. Watkin,Donna E. Stewart
出处
期刊:The Journal of Clinical Psychiatry [Physicians Postgraduate Press, Inc.]
卷期号:67 (05): 761-770 被引量:42
标识
DOI:10.4088/jcp.v67n0510
摘要

A number of studies have suggested potential gender differences in the efficacy of antidepressant medications. Pooled data from double-blind, placebo-controlled studies were utilized to compare the efficacy of duloxetine in the treatment of major depressive disorder (MDD) in male and female patients.Efficacy data were pooled from 7 randomized, double-blind, placebo-controlled clinical trials of duloxetine. These studies represent all available data from U.S. acute-phase, placebo-controlled studies of duloxetine for the treatment of MDD. Patients (aged > or = 18 years) meeting DSM-IV criteria for MDD received duloxetine (40-120 mg/day; men, N = 318; women, N = 578) or placebo (men, N = 242; women, N = 484) for up to 9 weeks. Efficacy measures included the 17-item Hamilton Rating Scale for Depression (HAM-D17) total score, HAM-D17 subscales (core, Maier, anxiety, retardation, sleep), the Clinical Global Impressions-Severity of Illness scale (CGI-S) and Patient Global Impression of Improvement scale (PGI-I), the Quality of Life in Depression Scale (QLDS), and Visual Analog Scales (VAS) for pain. The first patient visit was February 1, 1999, and the last patient visit was November 27, 2002.In both male and female patients, duloxetine produced significantly greater improvement in HAM-D17, CGI-S, and PGI-I when compared with placebo (p < .05). Treatment-by-gender interactions did not reach statistical significance, indicating that the magnitude of duloxetine's treatment effects did not differ significantly between male and female patients. However, there was a trend for female patients to show a more robust response than male patients to both duloxetine and placebo. On the basis of VAS assessments of pain severity, duloxetine-treated female patients appeared to exhibit greater improvement than male patients, while women receiving placebo had smaller responses than placebo-treated men. Improvements in quality of life were significantly greater for both men (p = .006) and women (p = .001) receiving duloxetine than placebo and showed no significant difference by gender.In this analysis of pooled data, the efficacy of duloxetine did not differ significantly in male and female patients.

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