Department of Psychiatry and Psychotherapy, University Hospital Hamburg-Eppendorf, Germany.
J Psychiatr Res. 2010 Apr;44(6):339-46. doi: 10.1016/j.jpsychires.2009.10.006. Epub 2009 Nov 11.
Preclinical and clinical studies have suggested a role of the mineralocorticoid receptor (MR) in the response to antidepressants. We tested in a proof-of-concept study whether adding fludrocortisone (an MR agonist) or spironolactone (an MR antagonist) accelerates onset of action and improves efficacy of escitalopram in patients with major depression. We included 64 in- and outpatients with major depression (Hamilton Depression Scale-17 score>18) in a double-blind, randomized, placebo-controlled trial. Patients were randomized in a 2:2:1 fashion to fludrocortisone (0.2 mg/d, n=24) or spironolactone (100 mg/d, n=27) or placebo (n=13) for the first 3 weeks during a 5-week treatment with escitalopram. No differences in mean HAMD change scores and in time to response emerged between treatments. However, among the responders, patients treated with fludrocortisone responded faster (Breslow test, p=0.05). The mean number of days to response was 16.0+/-2.6 days vs. placebo 22.2+/-2.0 vs. spironolactone 22.6+/-2.3 (F=3.78, p=0.03). In the whole group, plasma cortisol increased during spironolactone and decreased during fludrocortisone treatment (F=2.4, p=0.04). In patients treated with fludrocortisone, non-responders had elevated cortisol values compared to responders throughout the study period (F=5.1, p=0.04). Stimulation of MR with fludrocortisone as adjunct to escitalopram accelerated the response in the group of responders while no effect emerged in the sample as a whole. A larger randomized controlled trial is warranted.
临床前和临床研究表明,盐皮质激素受体(MR)在抗抑郁药的反应中起作用。我们在一项概念验证研究中测试了在重度抑郁症患者中添加氟氢可的松(MR 激动剂)或螺内酯(MR 拮抗剂)是否可以加速起效并提高依西酞普兰的疗效。我们在一项双盲、随机、安慰剂对照试验中纳入了 64 名住院和门诊重度抑郁症患者(汉密尔顿抑郁量表-17 评分>18)。患者以 2:2:1 的比例随机分为氟氢可的松(0.2mg/d,n=24)、螺内酯(100mg/d,n=27)或安慰剂(n=13)组,在前 3 周与依西酞普兰治疗 5 周。在治疗期间,各组的平均 HAMD 变化评分和反应时间无差异。然而,在应答者中,接受氟氢可的松治疗的患者应答更快(Breslow 检验,p=0.05)。应答者的平均反应天数为 16.0+/-2.6 天,安慰剂组为 22.2+/-2.0 天,螺内酯组为 22.6+/-2.3 天(F=3.78,p=0.03)。在整个组中,螺内酯治疗期间血浆皮质醇增加,氟氢可的松治疗期间皮质醇减少(F=2.4,p=0.04)。在接受氟氢可的松治疗的患者中,与应答者相比,无应答者在整个研究期间的皮质醇值升高(F=5.1,p=0.04)。用氟氢可的松刺激 MR 作为依西酞普兰的辅助治疗,在应答者组中加速了反应,而在整个样本中没有出现效果。需要更大规模的随机对照试验。