Kennedy Sidney H, Fulton Kari A, Bagby R Michael, Greene Andrea L, Cohen Nicole L, Rafi-Tari Shahryar
University of Toronto, Ontario.
Can J Psychiatry. 2006 Mar;51(4):234-42. doi: 10.1177/070674370605100405.
The primary objective was to evaluate sexual function (SF) separately in men and women with major depressive disorder (MDD) before and during treatment with bupropion sustained release (SR) or paroxetine. The secondary objectives involved a comparative evaluation of the Sex Effects Scale (Sex FX) and the Investigator-Rated Sexual Desire and Functioning Scale (IRSD-F), as well as a comparison of antidepressant outcomes and an examination of the relation between level of depression and SF over time.
There were 141 patients (68 women and 73 men) who met DSM-IV criteria for a current major depressive episode. They were randomly assigned to receive bupropion SR (150 to 300 mg daily) or paroxetine (20 to 40 mg daily) under double-blind trial conditions. Patients were assessed at baseline and at 2, 4, 6, and 8 weeks with the 17-item Hamilton Depression Rating Scale (HDRS17), Sex FX, and IRSD-F.
Prior to treatment, women reported significantly lower SF on both the Sex FX and IRSD-F scales, compared with men. During treatment, there were no significant drug differences on measures of SF over time for women; however, men who were treated with paroxetine reported a worsening of SF, whereas bupropion SR did not significantly alter SF. Both bupropion SR and paroxetine produced clinically and statistically significant reductions in HDRS17 scores as well as comparable rates of response and remission. There was a statistically significant correlation between the 2 measures of SF at all visits. There was also a significant inverse relation between depression and SF in women, but not in men, irrespective of drug.
According to the Sex FX scale, a significant difference in antidepressant-related sexual dysfunction was detected in men, but not women, during treatment with bupropion SR or paroxetine.
主要目的是分别评估患有重度抑郁症(MDD)的男性和女性在接受安非他酮缓释片(SR)或帕罗西汀治疗之前及治疗期间的性功能(SF)。次要目的包括对性效应量表(Sex FX)和研究者评定的性欲与性功能量表(IRSD - F)进行比较评估,以及比较抗抑郁疗效,并考察抑郁程度与性功能随时间的关系。
有141名符合当前重度抑郁发作的DSM - IV标准的患者(68名女性和73名男性)。在双盲试验条件下,他们被随机分配接受安非他酮SR(每日150至300毫克)或帕罗西汀(每日20至40毫克)治疗。患者在基线以及第2、4、6和8周时使用17项汉密尔顿抑郁评定量表(HDRS17)、Sex FX和IRSD - F进行评估。
治疗前,与男性相比,女性在Sex FX和IRSD - F量表上报告的性功能显著更低。治疗期间,女性在性功能测量指标上随时间推移没有显著的药物差异;然而,接受帕罗西汀治疗的男性报告性功能恶化,而安非他酮SR未显著改变性功能。安非他酮SR和帕罗西汀均使HDRS17评分在临床和统计学上有显著降低,以及有相当的有效率和缓解率。在所有访视中,两种性功能测量指标之间存在统计学上的显著相关性。无论使用何种药物,女性的抑郁与性功能之间也存在显著的负相关,但男性不存在。
根据Sex FX量表,在使用安非他酮SR或帕罗西汀治疗期间,男性而非女性检测到与抗抑郁药相关的性功能障碍存在显著差异。