Department of Psychiatry, Vancouver Hospital, Vancouver, British Columbia, Canada.
Menopause. 2010 Sep-Oct;17(5):962-71. doi: 10.1097/gme.0b013e3181d59765.
Although suspected, androgen deficit in women with sexual dysfunction has never been established. Given that serum testosterone levels are of limited value, we sought to compare total androgen activity in women with and without hypoactive sexual desire disorder (HSDD). Intracellular production in target tissues is the major source of testosterone in older women and can now be measured. Androgen metabolites, specifically androsterone glucuronide (ADT-G), reflect intracellular and ovarian sources of testosterone. Thus, we predicted significantly lowered levels of metabolites in women with sexual dysfunction.
A detailed assessment of the sexual function of women without depression, without serious relationship discord, or receiving medications affecting sexual function included 121 women with HSDD and 124 sexually healthy community controls. Sexual function was assessed using structured interviews, validated questionnaires, and steroid analysis-mass spectrometry levels of ADT-G, testosterone, and precursor hormones.
No group differences in serum levels of testosterone or ADT-G were found. Significantly lower levels of two precursor hormones, dehydroepiandrosterone sulfate and androstene-3β,17β-diol, were found in women with sexual dysfunction (P = 0.006 and P = 0.020, respectively). The variability of metabolite and precursor levels was substantial for all women.
Significantly lower levels of the two precursor steroids dehydroepiandrosterone sulfate and androstene-3β,17β-diol but not the major androgen metabolite ADT-G were found in women with HSDD. Although the significance of the former awaits further study, androgen deficiency in women with HSDD was not confirmed. Given the unknown long-term effects of testosterone supplementation, women receiving testosterone therapy should be informed that a deficit of testosterone activity in women with HSDD has not been identified.
尽管怀疑女性性功能障碍与雄激素缺乏有关,但从未得到证实。由于血清睾酮水平的价值有限,我们试图比较性欲减退障碍(HSDD)女性与无 HSDD 女性的总雄激素活性。在老年女性中,细胞内产生是睾酮的主要来源,现在可以进行测量。雄激素代谢物,特别是雄酮葡萄糖醛酸(ADT-G),反映了睾酮的细胞内和卵巢来源。因此,我们预测性功能障碍女性的代谢物水平会显著降低。
对无抑郁、无严重关系不和或服用影响性功能药物的女性进行详细的性功能评估,包括 121 名 HSDD 女性和 124 名性功能健康的社区对照。使用结构化访谈、经过验证的问卷和类固醇分析-质谱法评估 ADT-G、睾酮和前体激素的水平,来评估性功能。
未发现血清睾酮或 ADT-G 水平存在组间差异。性功能障碍女性的两种前体激素脱氢表雄酮硫酸酯和雄烯二酮-3β,17β-二醇水平显著降低(分别为 P=0.006 和 P=0.020)。所有女性的代谢物和前体水平的变异性都很大。
在 HSDD 女性中发现两种前体类固醇脱氢表雄酮硫酸酯和雄烯二酮-3β,17β-二醇水平显著降低,但主要雄激素代谢物 ADT-G 水平没有降低。虽然前者的意义有待进一步研究,但 HSDD 女性的雄激素缺乏并未得到证实。鉴于睾酮补充的未知长期影响,应告知接受睾酮治疗的女性,HSDD 女性的雄激素活性缺乏尚未确定。