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首页> 外文期刊>Journal of clinical psychopharmacology >Analysis by Age and Sex of Efficacy Data From Placebo-Controlled Trials of Desvenlafaxine in Outpatients With Major Depressive Disorder
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Analysis by Age and Sex of Efficacy Data From Placebo-Controlled Trials of Desvenlafaxine in Outpatients With Major Depressive Disorder

机译:从抑郁症对抗治疗中的疗效数据的年龄和性别分析,从抑郁症的外分门诊患者

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This pooled analysis evaluated the efficacy of desvenlafaxine (administered as desvenlafaxine succinate) for the treatment of major depressive disorder (MDD) in patients grouped by age and sex. Nine clinical trials were pooled. Outpatients 18 years or older with MDD received desvenlafaxine 50, 100, 200, or 400 mg/d (men = 709; women = 1096) or placebo (men = 399; women = 709) for 8 weeks. Data were analyzed by sex and by age groups of 40 years and younger, 41 to 54 years, 55 to 64 years, and 65 years and older. The primary outcome was change from baseline in the 17-item Hamilton Rating Scale for Depression (HAM-D17) total score at the final evaluation. Secondary measures included response (>50% reduction in HAM-D]7) and remission (HAM-D <7). No significant sex-treatment, age-treatment, or sex-age-treatment interactions were observed. Differences in the HAM-D change from baseline for desvenlafaxine versus placebo were -1.72 for women (P < 0.001) and -2.11 for men (P < 0.001); these changes were significant among women of the 18-to-40 (P = 0.01), 41-to-54 (P = 0.002), and 65-years-and-older subgroups (P = 0.02), and significant among men for the 18-to-40 (P = 0.03) and 41-to-54 subgroups (P = 0.002). The response rates for desvenlafaxine and placebo were 53% and 42% (P < 0.001), respectively, among women, and 53% and 41% (P < 0.001), respectively, among men; the remission rates were 31% and 21% (P < 0.001) and 34% and 26% (P = 0.007), respectively. The response rates were similar across age subgroups, with significant differences from placebo observed in the 18-to-40 (P < 0.05), 41-to-54 (P < 0.005), and 65-and-older subgroups (P = 0.02). The remission rates were significant versus placebo in the 41-to-54 (P = 0.006), 55-to-64 (P = 0.01), and 65-and-older (P = 0.02) subgroups among women but not in any age subgroup among men. Desvenlafaxine generally improved depressive symptoms across age and sex subgroups.
机译:该汇总分析评估了Desvenlafaxine(给予Desvenlafaxine琥珀酸盐)治疗年龄和性别分组的患者的主要抑郁症(MDD)的疗效。合并九项临床试验。 MDD 18岁或以上的门诊患者接受了Desvenlafaxine 50,100,200或400 mg / d(Men = 709;女性= 1096)或安慰剂(MEN = 399;女性= 709)8周。数据通过性别和40岁以上的年龄分析,41至54岁,55至64岁,65岁及以上。主要结果是从基线改变了17项汉密尔顿评级规模的抑郁症(Ham-D17)在最终评估中的总分。次要措施包括响应(HAM-D减少> 50%] 7)和缓解(HAM-D <7)。没有观察到性治疗,年龄治疗或性龄治疗相互作用。来自贫民党基线的HAM-D变化的差异为-1.72女性(P <0.001)和-2.11用于男性(P <0.001);这些变化在18至40(p = 0.01),41-54(p = 0.002)和65年和较旧的亚组(P = 0.02)中,以及男性中的重要性18至40(p = 0.03)和41至54个亚组(p = 0.002)。在男性中分别分别为53%和4.0%(p <0.1%(p <0.001),分别为53%和42%(p <0.001),分别为53%和4.001);缓解率分别为31%和21%(P <0.001)和34%和26%(P = 0.007)。亚组亚组相似的响应率与安慰剂观察到18至40(P <0.05),41-54(P <0.005)和65岁和较旧的亚组观察到的显着差异(P = 0.02 )。缓解率在41至54(p = 0.006)中的缓解率显着,55至64(p = 0.01),65岁和较旧的(p = 0.02)个亚组,但不在任何年龄男人之间的亚组。 Desvenlafaxine通常改善患有年龄和性亚组的抑郁症状。

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