Aversa Antonio, Isidori Andrea M, Spera Giovanni, Lenzi Andrea, Fabbri Andrea
AFaR-CRCCS, Ospedale Fatebenefratelli Isola Tiberina, Rome, Italy.
Clin Endocrinol (Oxf). 2003 May;58(5):632-8. doi: 10.1046/j.1365-2265.2003.01764.x.
We have recently shown that, in men with erectile dysfunction (ED), free testosterone (FT) directly correlates with penile arterial inflow. This led us to further investigate the effect(s) of androgen administration on cavernous arteries in patients failing sildenafil treatment.
Prospective randomized placebo-controlled pilot study.
Twenty patients with arteriogenic ED as evaluated by dynamic colour duplex ultrasound (D-CDU) studies, normal sexual desire but testosterone (T) and FT in the lower quartile of normal range (low-normal), not responding to sildenafil treatment (100 mg) on six consecutive attempts.
All patients had D-CDU, hormonal [LH, prostate-specific antigen (PSA), total and free testosterone, sex hormone-binding protein (SHBG), oestradiol], biochemical [haematocrit, low-density lipoprotein (LDL) and HDL cholesterol, triglycerides], and sexual evaluations [International Index of Erectile Function (IIEF)] before and after 1 month of therapy with transdermal testosterone (5 mg/day, n = 10) or placebo along with sildenafil treatment on demand. Measurement of flow parameters by D-CDU on cavernous arteries was the primary endpoint of the study. Improvement of erectile function was assessed using the IIEF questionnaire and the Global Assessment Question (GAQ).
One month treatment with transdermal testosterone led to a significant increase in T and FT levels (23.7 +/- 3.3 SD vs. 12.8 +/- 2.1 nmol/l and 473 +/- 40.2 vs. 260 +/- 18.1 pmol/l, P < 0.01, respectively). In addition testosterone administration induced a significant increase in arterial inflow to cavernous arteries measured by D-CDU (32 +/- 3.6 vs. 25.2 +/- 4 cm/s, P < 0.05), with no adverse effects. Also, a significant improvement in erectile function domain score at IIEF was found in the androgen but not in the placebo-treated patients (21.8 +/- 2.1 vs. 14.4 +/- 1.4, P < 0.05) which was associated with significant changes in the GAQ score (80%vs. 10%, P < 0.01).
In patients with arteriogenic ED and low-normal androgen levels, short-term testosterone administration increases T and FT levels and improves the erectile response to sildenafil likely by increasing arterial inflow to the penis during sexual stimulation.
我们最近发现,在勃起功能障碍(ED)男性中,游离睾酮(FT)与阴茎动脉血流直接相关。这促使我们进一步研究雄激素给药对西地那非治疗失败患者海绵体动脉的影响。
前瞻性随机安慰剂对照试验研究。
通过动态彩色双功超声(D-CDU)检查评估为动脉性ED的20例患者,性欲正常,但睾酮(T)和FT处于正常范围的下四分位数(低正常),连续6次尝试对西地那非治疗(100mg)无反应。
所有患者在接受经皮睾酮(5mg/天,n = 10)或安慰剂治疗1个月前后,以及根据需要进行西地那非治疗前后,均进行了D-CDU检查、激素检查[促黄体生成素(LH)、前列腺特异性抗原(PSA)、总睾酮和游离睾酮、性激素结合蛋白(SHBG)、雌二醇]、生化检查[血细胞比容、低密度脂蛋白(LDL)和高密度脂蛋白胆固醇、甘油三酯]以及性功能评估[国际勃起功能指数(IIEF)]。通过D-CDU测量海绵体动脉的血流参数是本研究的主要终点。使用IIEF问卷和总体评估问题(GAQ)评估勃起功能的改善情况。
经皮睾酮治疗1个月导致T和FT水平显著升高(分别为23.7±3.3 SD vs. 12.8±2.1 nmol/l和473±40.2 vs. 260±18.1 pmol/l,P < 0.01)。此外,给予睾酮导致通过D-CDU测量的海绵体动脉血流显著增加(32±3.6 vs. 25.2±4 cm/s,P < 0.05),且无不良反应。此外,雄激素治疗组患者的IIEF勃起功能领域评分显著改善,而安慰剂治疗组患者未改善(21.8±2.1 vs. 14.4±1.4,P < 0.05),这与GAQ评分的显著变化相关(80% vs. 10%,P < 0.01)。
在动脉性ED且雄激素水平低正常的患者中,短期给予睾酮可提高T和FT水平,并可能通过增加性刺激期间阴茎的动脉血流来改善对西地那非的勃起反应。