Sex-controlled differences in sertraline and citalopram efficacies in major depressive disorder: a randomized, double-blind trial.

IF 2.1 3区 医学 Q3 PHARMACOLOGY & PHARMACY International Clinical Psychopharmacology Pub Date : 2024-04-18 DOI:10.1097/yic.0000000000000550
Ahmad Shamabadi, Hanie Karimi, Mohammad Ali Fallahzadeh, Salar Vaseghi, Razman Arabzadeh Bahri, Bita Fallahpour, Amir Hossein Abdolghaffari, Shahin Akhondzadeh
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Abstract

To investigate the response to antidepressants while controlling for sex, which has been controversial, 92 outpatient males and females with major depressive disorder were assigned to sertraline (100 mg/day) or citalopram (40 mg/day) in two strata and were assessed using Hamilton depression rating scale (HDRS) scores and brain-derived neurotrophic factor (BDNF), interleukin (IL)-6 and cortisol serum levels in this 8-week, randomized, parallel-group, double-blind clinical trial. Data of 40 sertraline and 40 citalopram recipients with equal representation of males and females assigned to each medication were analyzed, while their baseline characteristics were not statistically different (P > 0.05). There were no significant differences between sertraline and citalopram recipients in outcome changes (P > 0.05), all of which indicated improvement, but a significant time-treatment-sex interaction effect in BDNF levels was observed (P = 0.035). Regarding this, subgroup analyses illustrated a significantly greater increase in male BDNF levels following sertraline treatment (P = 0.020) with a moderate to large effect size (Cohen's d = 0.76 and ). Significant associations were observed between percentage changes in IL-6 levels and BDNF levels in sertraline recipients (P = 0.033) and HDRS scores in citalopram recipients (P < 0.001). Sex was an effect modifier in BDNF alterations following sertraline and citalopram administration. Further large-scale, high-quality, long-term studies are recommended.
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舍曲林和西酞普兰对重度抑郁症疗效的性别差异:随机双盲试验。
为了研究在控制性别因素的同时对抗抑郁药的反应(性别因素一直存在争议),92 名患有重度抑郁症的男性和女性门诊患者被分成两组,分别服用舍曲林(100 毫克/天)或西酞普兰(40 毫克/天),并使用汉密尔顿抑郁评分量表(HDRS)得分和脑源性神经营养因子(BDNF)进行评估、在这项为期 8 周的随机、平行分组、双盲临床试验中,研究人员使用汉密尔顿抑郁评分量表 (HDRS) 评分、脑源性神经营养因子 (BDNF) 和白细胞介素 (IL)-6 以及皮质醇血清水平进行了评估。分析了40名舍曲林和40名西酞普兰受试者的数据,两种药物的受试者男女比例相等,而他们的基线特征没有统计学差异(P> 0.05)。舍曲林和西酞普兰受试者在结果变化方面没有明显差异(P > 0.05),所有结果均显示病情有所改善,但在BDNF水平方面观察到了明显的时间-治疗-性别交互效应(P = 0.035)。关于这一点,亚组分析表明,在舍曲林治疗后,男性的 BDNF 水平明显增加(P = 0.020),效应大小为中度到大型(Cohen's d = 0.76 和 )。在舍曲林受试者中,IL-6水平的百分比变化与BDNF水平之间存在显著关联(P = 0.033),在西酞普兰受试者中,HDRS评分与IL-6水平的百分比变化之间也存在显著关联(P < 0.001)。在服用舍曲林和西酞普兰后,性别是BDNF改变的一个效应调节因子。建议进一步开展大规模、高质量的长期研究。
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来源期刊
CiteScore
4.40
自引率
23.10%
发文量
97
审稿时长
>12 weeks
期刊介绍: International Clinical Psychopharmacology provides an essential link between research and clinical practice throughout psychopharmacology. It reports on studies in human subjects, both healthy volunteers and patients, which relate the effects of drugs on psychological processes. A major objective of the journal is to publish fully refereed papers which throw light on the ways in which the study of psychotropic drugs can increase our understanding of psychopharmacology. To this end the journal publishes results of early Phase I and II studies, as well as those of controlled clinical trials of psychotropic drugs in Phase II and IV. Other topics covered include the epidemiology of psychotropic drug prescribing and drug taking, the sociology of psychotropic drugs including compliance, and research into the safety and adverse effects of these compounds.
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