Boyarsky B K, Haque W, Rouleau M R, Hirschfeld R M
University of Texas Medical Branch, Galveston, USA.
Depress Anxiety. 1999;9(4):175-9. doi: 10.1002/(sici)1520-6394(1999)9:4<175::aid-da5>3.0.co;2-0.
One-third of patients with untreated depression have sexual difficulties manifested by decreased libido, erectile dysfunction or delayed ejaculation. This dysfunction may be exacerbated by stimulation of post-synaptic serotonin 5HT2 receptors, a side-effect of most widely-used antidepressant medications, especially the selective serotonin reuptake inhibitors (SSRIs). Mirtazapine is an atypical antidepressant with alpha 2 adrenergic antagonist and serotonin 5-HT2 and 5-HT3 receptor-blocking activity. In theory, it should not worsen and perhaps may improve sexual function. This pilot study investigated sexual functioning and antidepressant activity in depressed patients taking mirtazapine.
Twenty-five (F = 18, M = 7) sexually active adult outpatients with a DSM-IV-diagnosis of major depressive episode entered a 12-week, flexible-dosing, open-label pilot study. The Arizona Sexual Experiences Scale (ASEX) assessed sexual functioning and the Hamilton Depression Rating Scale (HAM-D) assessed depressive symptoms on a bimonthly basis.
Desire, arousal/lubrication, and ease/satisfaction of orgasm improved (by 41%, 52%, and 48%, respectively) in the depressed women. In men, desire, arousal/erection, and ease/satisfaction of orgasm also improved (by 10%, 23% and 14%, respectively) but much more modestly. HAM-D, Clinical Global Impression (CGI) Sheehan Disability Scale (SDS), and Symptom Checklist-90 (SCL-90) scores improved in both groups. There was a 50% dropout rate among women before six weeks of treatment. However, the ASEX and HAM-D scores of the groups terminating before and after six weeks of treatment showed similar rates of improvement.
Mirtazapine has a beneficial effect on sexual functioning in both depressed women and men. Longer-term double-blind research assessing sexual function during the administration of mirtazapine as well as other antidepressants is recommended.
三分之一未经治疗的抑郁症患者存在性功能障碍,表现为性欲减退、勃起功能障碍或射精延迟。这种功能障碍可能会因突触后5-羟色胺2(5HT2)受体受刺激而加剧,这是大多数广泛使用的抗抑郁药物的副作用,尤其是选择性5-羟色胺再摄取抑制剂(SSRI)。米氮平是一种非典型抗抑郁药,具有α2肾上腺素能拮抗剂以及5-羟色胺2和5-羟色胺3受体阻断活性。理论上,它不应使性功能恶化,甚至可能改善性功能。这项初步研究调查了服用米氮平的抑郁症患者的性功能及抗抑郁活性。
25名(女性18名,男性7名)有性活动的成年门诊患者,根据《精神疾病诊断与统计手册》第四版(DSM-IV)诊断为重度抑郁发作,进入一项为期12周的灵活剂量开放标签初步研究。亚利桑那性体验量表(ASEX)评估性功能,汉密尔顿抑郁评定量表(HAM-D)每两个月评估一次抑郁症状。
抑郁女性的性欲、性唤起/润滑以及性高潮的轻松程度/满意度有所改善(分别提高了41%、52%和48%)。男性的性欲、性唤起/勃起以及性高潮的轻松程度/满意度也有所改善(分别提高了10%、23%和14%),但改善程度要小得多。两组的HAM-D、临床总体印象(CGI)希恩残疾量表(SDS)和症状自评量表90(SCL-90)得分均有所改善。治疗六周前女性的脱落率为50%。然而,治疗六周前后终止治疗组的ASEX和HAM-D得分显示出相似的改善率。
米氮平对抑郁女性和男性的性功能均有有益影响。建议进行长期双盲研究,评估服用米氮平以及其他抗抑郁药物期间的性功能。