未经治疗的重度抑郁症男性患者的精神神经内分泌特征及其与治疗效果和性副作用的关系

Kristian H.Reveles Jensen , Malene Ravn Aarestrup , Søren Vinther Larsen , Kristin Köhler-Forsberg , Gitte Moos Knudsen , Martin Balslev Jørgensen , Vibe G. Frokjaer
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引用次数: 0

摘要

性激素可能与重度抑郁障碍(MDD)有关,因为在抑郁风险、症状和治疗效果方面存在性别差异。有关荷尔蒙对重度抑郁症的影响的研究主要集中在女性身上,很少涉及男性。因此,我们研究了未经治疗的男性 MDD 患者体内的睾酮和雌二醇水平是否与抑郁症状、SSRI 治疗反应和性副作用有关。研究人员采集了 26 名未服药男性(18-49 岁)的治疗前血浆睾酮和雌二醇。患者接受 10-20 毫克艾司西酞普兰治疗,为期 12 周。抑郁严重程度通过汉密尔顿抑郁量表 17(HAMD17)进行测量,治疗反应为 HAMD6 与基线相比的变化。性副作用采用标准化的临床医生评分表进行评估。治疗前睾酮与抑郁严重程度呈正相关(p = 0.016),这种关联主要由植物神经症状:体重减轻、胃肠道症状和失眠(p ≤ 0.027)驱动。治疗前的性激素水平与抗抑郁治疗结果无关。然而,在接受依西酞普兰治疗 8-12 周后出现性副作用的患者中,治疗前性激素水平较低;低雌二醇与勃起和射精功能障碍有关(p = 0.039),低睾酮和低雌二醇均与性欲下降有关(p ≤ 0.004)。总之,我们发现患有多发性抑郁症的男性睾酮低与抑郁症的严重程度有关,尤其是植物神经症状。然而,治疗前的性激素水平与治疗效果无关,而与性副作用有关。综上所述,我们的研究结果强调性激素谱是SSRI诱发性功能障碍的潜在预后生物标志物。数据来自临床研究(NCT02869035)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Psychoneuroendocrine profiles of unmedicated men with major depressive disorder and associations to treatment effects and sexual side-effects

Psychoneuroendocrine profiles of unmedicated men with major depressive disorder and associations to treatment effects and sexual side-effects

Sex hormones are potentially involved in major depressive disorder (MDD) as there are sex differences in risk for depression, symptomatology and treatment efficacy. Such hormonal contributions to MDD have mainly been studied in women and scarcely in men. We, therefore, investigate whether testosterone and estradiol levels in unmedicated men with MDD are associated with depressive symptom profiles, SSRI treatment response, and sexual side-effects. Pretreatment plasma testosterone and estradiol were available from 26 unmedicated men (age 18–49). The patients were treated with 10–20 mg escitalopram for 12 weeks. Depression severity was measured by Hamilton Depression Rating Scale 17 (HAMD17), and treatment response was the change in HAMD6 from baseline. Sexual side-effects were assessed with a standardized clinician-rated scale. Pretreatment testosterone was positively associated with depression severity (p = 0.016), the association was primarily driven by vegetative symptoms: weight loss, gastrointestinal symptoms, and insomnia (p ≤ 0.027). Pretreatment sex hormone levels were not associated with antidepressant treatment outcome. However, pretreatment sex hormones were lower in patients who experienced sexual side-effects after 8–12 weeks of escitalopram treatment; low estradiol was associated with erectile and ejaculatory dysfunction (p = 0.039) and low testosterone and low estradiol were both associated with decreased libido (p ≤ 0.004). In conclusion, we find low testosterone in men with MDD coupled with depression severity, particularly vegetative symptoms. However, pretreatment sex hormone levels were not associated with treatment efficacy but with sexual side-effects. Taken together, our findings highlight sex hormone profiles as potential prognostic biomarkers of SSRI-induced sexual dysfunction.

Data from

Clinical study (NCT02869035).

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