Huang Jia, Wang Yun, Chen Jun, Zhang Yanlei, Yuan Zheng, Yue Li, Haro Josep Maria, Moneta Maria Victoria, Novick Diego, Fang Yiru
Division of Mood Disorders, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China,
Medical Department, Eli Lilly and Company, Shanghai, China.
Neuropsychiatr Dis Treat. 2018 Sep 26;14:2473-2484. doi: 10.2147/NDT.S159800. eCollection 2018.
To compare treatment outcomes in patients with major depressive disorder treated with duloxetine, escitalopram, fluoxetine, paroxetine, or sertraline for up to 6 months.
Data were taken from a 6-month prospective, observational study that included 1,549 major depressive disorder patients without sexual dysfunction in 12 countries. We report the overall results and those from Asian countries. Depression severity was measured using the Clinical Global Impression and the 16-item Quick Inventory of Depressive Symptomatology Self-Report (QIDS-SR). Clinical and functional remissions were defined as having a QIDS-SR <6, and as having a rating of <3 on all three Sheehan Disability Scale items and no reduced productivity, respectively. Mixed effects modeling with repeated measures analysis and generalized estimating equation models were used. Propensity scores were included in the models.
The mixed effects modeling with repeated measures regression models showed that the Clinical Global Impression rating during follow-up was significantly lower in those patients treated with duloxetine compared with escitalopram (0.40, 95% CI 0.25 to 0.56); fluoxetine (0.22, 95% CI 0.05 to 0.38); paroxetine (0.38, 95% CI 0.23 to 0.54); and sertraline (0.32, 95% CI 0.16 to 0.49). The QIDS-SR of duloxetine-treated patients was significantly lower than those treated with escitalopram (1.58, 95% CI 1.03 to 2.12); fluoxetine (1.48, 95% CI 0.90 to 2.06); paroxetine (1.53, 95% CI 1.00 to 2.07); and sertraline (1.19, 95% CI 0.61 to 1.78). The probability of clinical remission of the patients treated with escitalopram, fluoxetine, paroxetine, and sertraline was lower than those treated with duloxetine (OR 0.46, 95% CI 0.33 to 0.64; OR 0.42, 95% CI 0.29 to 0.61; OR 0.40, 95% CI 0.29 to 0.56; OR 0.50, 95% CI 0.35 to 0.71; respectively). The regression analysis of functional remission also showed more favorable results for duloxetine, with OR ranging from 0.43, 95% CI 0.31 to 0.60 for paroxetine to 0.49, 95% CI 0.35 to 0.70 for sertraline. The results for the Asian countries were generally consistent.
Duloxetine-treated patients had better 6-month outcomes in terms of depression severity and clinical and functional remission, compared with selective serotonin reuptake inhibitor-treated patients.
比较接受度洛西汀、艾司西酞普兰、氟西汀、帕罗西汀或舍曲林治疗长达6个月的重度抑郁症患者的治疗效果。
数据来自一项为期6个月的前瞻性观察性研究,该研究纳入了12个国家的1549名无性功能障碍的重度抑郁症患者。我们报告总体结果以及来自亚洲国家的结果。使用临床总体印象量表和16项抑郁症状快速自评量表(QIDS-SR)来测量抑郁严重程度。临床缓解和功能缓解分别定义为QIDS-SR<6,以及在希恩残疾量表的所有三个项目上评分<3且生产力未降低。使用重复测量分析的混合效应模型和广义估计方程模型。模型中纳入了倾向得分。
重复测量回归模型的混合效应模型显示,与艾司西酞普兰相比,接受度洛西汀治疗的患者在随访期间的临床总体印象评分显著更低(0.40,95%置信区间0.25至0.56);与氟西汀相比(0.22,95%置信区间0.05至0.38);与帕罗西汀相比(0.38,95%置信区间0.23至0.54);与舍曲林相比(0.32,95%置信区间0.16至0.49)。接受度洛西汀治疗的患者的QIDS-SR显著低于接受艾司西酞普兰治疗的患者(1.58,95%置信区间1.03至2.12);低于接受氟西汀治疗的患者(1.48,95%置信区间0.90至2.06);低于接受帕罗西汀治疗的患者(1.53,95%置信区间1.00至2.07);低于接受舍曲林治疗的患者(1.19,95%置信区间0.61至1.78)。接受艾司西酞普兰、氟西汀、帕罗西汀和舍曲林治疗的患者的临床缓解概率低于接受度洛西汀治疗的患者(比值比分别为0.46,95%置信区间0.33至0.64;0.42,95%置信区间0.29至0.61;0.40,95%置信区间0.29至0.56;0.50,95%置信区间0.35至0.71)。功能缓解的回归分析也显示度洛西汀的结果更有利,比值比范围从帕罗西汀的0.43,95%置信区间0.31至0.60到舍曲林的0.49,95%置信区间0.35至0.70。亚洲国家的结果总体一致。
与选择性5-羟色胺再摄取抑制剂治疗的患者相比,接受度洛西汀治疗的患者在抑郁严重程度以及临床和功能缓解方面有更好的6个月治疗效果。