University Health Network-Psychiatry, Toronto, ON, Canada.
J Sex Med. 2010 Oct;7(10):3449-59. doi: 10.1111/j.1743-6109.2010.01938.x.
Flibanserin, a novel 5-HT(1A) agonist and 5-HT(2A) antagonist, has the potential to treat sexual dysfunction.
Provide historical perspective on the rationale for development of flibanserin to treat sexual dysfunction, based on post hoc analyses of data.
The Arizona Sexual Experiences (ASEX) scale and the Hamilton depression rating scale (HAMD) Genital Symptoms item.
Sexual function outcomes are presented from four double-blind, randomized controlled studies involving a total of 369 men and 523 women diagnosed with Major Depressive Disorder. Each study had an active treatment arm to confirm assay sensitivity on the primary antidepressive endpoint. Two studies placebo, flibanserin (50mg bid), or fluoxetine (20mg qd) for 6 weeks and two involved placebo, flibanserin (50-100mg bid), or paroxetine (20-40mg qd) for 8 weeks.
Individual study completion rates were 77-80%. At baseline, 38% of men and 67% of women reported sexual dysfunction. Assay sensitivity was not demonstrated in the fluoxetine trials and sexual function outcomes were inconsistent. Flibanserin and placebo were associated with low rates of treatment-emergent sexual dysfunction in women during the paroxetine studies. In one study, 70% of flibanserin-treated women with baseline sexual dysfunction reported improvement in sexual function, compared with 30% of placebo-treated women. Mean change from baseline on the HAMD "Genital Symptoms" item in one paroxetine study was significantly better among flibanserin- than placebo-treated women at weeks 4, 6, and 8 (P<0.05). Sexual function adverse events across flibanserin groups were generally comparable to placebo.
Although these studies were not designed or powered to compare sexual function outcomes, results suggested a potential benefit of flibanserin on sexual function, particularly on female sexual desire, and provided a rationale to evaluate the efficacy of flibanserin as a treatment for female hypoactive sexual desire disorder.
氟班色林是一种新型 5-HT(1A) 激动剂和 5-HT(2A) 拮抗剂,具有治疗性功能障碍的潜力。
基于事后分析数据,为开发氟班色林治疗性功能障碍提供理论依据。
亚利桑那性体验量表(ASEX)和汉密尔顿抑郁评定量表(HAMD)生殖器症状条目。
对四项共涉及 369 名男性和 523 名被诊断为重度抑郁症的患者的双盲、随机对照研究的性功能结果进行了评估。每个研究均有一个活性治疗组,以确认主要抗抑郁终点的检测灵敏度。两项研究采用安慰剂、氟班色林(50mg,每日两次)或氟西汀(20mg,每日一次)治疗 6 周,另外两项研究采用安慰剂、氟班色林(50-100mg,每日两次)或帕罗西汀(20-40mg,每日一次)治疗 8 周。
个别研究的完成率为 77-80%。基线时,38%的男性和 67%的女性报告存在性功能障碍。氟西汀试验未显示出检测灵敏度,性功能结果也不一致。在帕罗西汀研究中,氟班色林和安慰剂与女性治疗后出现的性功能障碍发生率低相关。在一项研究中,70%基线时存在性功能障碍的氟班色林治疗女性报告性功能改善,而安慰剂治疗女性为 30%。在一项帕罗西汀研究中,与安慰剂组相比,氟班色林组女性的汉密尔顿抑郁评定量表“生殖器症状”条目从基线的平均变化在第 4、6 和 8 周时显著更好(P<0.05)。氟班色林组的性功能不良事件与安慰剂组总体相当。
尽管这些研究并非旨在或有能力比较性功能结果,但结果表明氟班色林可能对性功能有益,尤其是对女性性欲,为评估氟班色林作为女性性欲低下障碍的治疗方法提供了依据。