Wu F C, Farley T M, Peregoudov A, Waites G M
University of Manchester, Manchester, United Kingdom.
Fertil Steril. 1996 Mar;65(3):626-36.
To evaluate the secondary impact of a prototype androgen contraceptive regimen on physical, metabolic and behavioral variables.
Prospective, open, noncomparative contraceptive efficacy study.
International multicenter study comprising 10 centers in seven countries.
Two hundred seventy-one healthy men, age 31.8 +/- 5.4 years (mean +/- SD), range 21 to 45 years.
Weekly IM injections of 200 mg T enanthate.
Adverse effects and discontinuations; biochemical and hematologic changes and interpopulation differences.
Chinese subjects were shorter and lighter and their baseline hemoglobin, plasma lipid, and liver enzyme levels were lower than in non-Chinese subjects. The most common side effects were painful injections, acne, fatigue, and weight gain. Gynecomastia and prostate problems were detected in 24 and 9 men, respectively, though no men stopped injections for such reasons. Testosterone enanthate increased body weight, hemoglobin, and urea but decreased testicular volume and creatinine. Plasma triglyceride, cholesterol, and low-density lipoprotein cholesterol were unchanged; high-density lipoprotein cholesterol decreased by 14% to 18% in non-Chinese but was unchanged in Chinese men. Liver transaminases were increased by 36% to 51% in Chinese but were unchanged in non-Chinese subjects. These T enanthate-induced effects were reversible within 6 months of stopping injections and were not related to the duration of T exposure.
Testosterone enanthate administration in a contraceptive trial produced significant but reversible effects on skin, muscle, liver, lipid metabolism, and hemopoietic functions that varied between population groups. These effects reflect the relatively high peak levels and fluctuations of plasma T produced by the weekly T enanthate regimen rather than an inherent feature of hormonal male contraception. The results highlight the need for long-acting preparations of T with more stable delivery kinetics.
评估一种原型雄激素避孕方案对身体、代谢和行为变量的继发性影响。
前瞻性、开放性、非对照避孕效果研究。
一项国际多中心研究,包括七个国家的10个中心。
271名健康男性,年龄31.8±5.4岁(均值±标准差),范围在21至45岁之间。
每周肌肉注射200mg庚酸睾酮。
不良反应和停药情况;生化和血液学变化以及人群间差异。
中国受试者较矮且体重较轻,其基线血红蛋白、血脂和肝酶水平低于非中国受试者。最常见的副作用是注射部位疼痛、痤疮、疲劳和体重增加。分别在24名和9名男性中检测到乳腺增生和前列腺问题,不过无人因此停止注射。庚酸睾酮使体重、血红蛋白和尿素增加,但使睾丸体积和肌酐降低。血浆甘油三酯、胆固醇和低密度脂蛋白胆固醇未发生变化;非中国男性的高密度脂蛋白胆固醇降低了14%至18%,而中国男性未发生变化。中国受试者的肝转氨酶升高了36%至51%,而非中国受试者未发生变化。这些庚酸睾酮诱导的效应在停止注射后6个月内可逆转,且与睾酮暴露时间无关。
在一项避孕试验中,庚酸睾酮给药对皮肤、肌肉、肝脏、脂质代谢和造血功能产生了显著但可逆的影响,不同人群组之间存在差异。这些效应反映了每周庚酸睾酮方案所产生的血浆睾酮相对较高的峰值水平和波动,而非激素男性避孕的固有特征。结果凸显了需要具有更稳定释放动力学的长效睾酮制剂。