首页> 外文期刊>Journal of Endocrinological Investigation: Official Journal of the Italian Society of Endocrinology >Comparison of a new long-acting testosterone undecanoate formulation vs testosterone enanthate for intramuscular androgen therapy in male hypogonadism.
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Comparison of a new long-acting testosterone undecanoate formulation vs testosterone enanthate for intramuscular androgen therapy in male hypogonadism.

机译:男性性腺功能减退症中肌内雄激素治疗的新长效十一烷酸睾丸激素制剂与庚酸睾丸酮制剂的比较。

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摘要

OBJECTIVE: To assess the efficacy and safety of a novel long-acting im testosterone undecanoate (TU) formulation in comparison with testosterone enanthate (TE). SUBJECTS AND METHODS: An open-label, randomized, prospective clinical trial in 40 hypogonadal men (baseline serum testosterone levels <5 nmol/l), randomly assigned to 250 mg TE/3 weeks (no.=20) or 1000 mg TU im every 6 to 9 weeks for 30 weeks (no.=20). Subsequently, 32/40 men continued the study for another 114 weeks, now receiving TU 1000 mg/12 weeks. RESULTS: TU and TE produced no statistically significant improvements in grip strength over the first 30 weeks, which only occurred after approximately 90 weeks when all subjects received TU. There were no changes in body mass index with TU and TE, neither in the follow-up period when all patients received TU. But ratios of waist to hip circumferences declined in the longer term. Total serum cholesterol, LDL cholesterol, and triglycerides declined over the first 30 weeks, while plasma HDL also declined. Plasma LDL decreased further under long-term TU therapy, while HDL then increased. Hemoglobin and hematocrit values significantly increased over the first 30 weeks in both treatment groups and then no further increase was observed. Levels did not exceed the upper limit of normal. In both treatment groups, serum prostate specific antigen levels rose slightly after 30 weeks, with no further increase over the first 12 months, remaining stable within the normal range. Plasma T before the following TU injection was above the lower limit of reference values. Four injections per year are adequate. CONCLUSIONS: Administration of TU every 12 weeks is at least as safe and efficacious for treatment of hypogonadal men as TE, with a substantially lower frequency of administration. Follow-up over 114 weeks, when all subjects received TU, showed an excellent profile of efficacy and safety.
机译:目的:评估与长效庚酸酯(TE)相比,新型长效十一酸睾丸激素制剂(TU)的疗效和安全性。受试者与方法:这项开放性,随机,前瞻性临床试验在40名性腺功能减退男性(基线血清睾丸激素水平<5 nmol / l)中进行,随机分配为250 mg TE / 3周(编号= 20)或1000 mg TU im每6至9周一次,共30周(编号= 20)。随后,有32/40名男性继续进行了114周的研究,现在接受TU 1000 mg / 12周。结果:TU和TE在开始的30周内没有产生统计学上的显着改善,仅在所有受试者接受TU后约90周后才发生。在所有患者接受TU的随访期内,TU和TE的体重指数均无变化。但是从长远来看,腰围与臀围的比率下降了。在最初的30周中,血清总胆固醇,低密度脂蛋白胆固醇和甘油三酸酯下降,而血浆高密度脂蛋白下降。在长期TU治疗下,血浆LDL进一步降低,而HDL随后升高。在两个治疗组的最初30周中,血红蛋白和血细胞比容值均显着升高,然后未观察到进一步的升高。含量未超过正常上限。在两个治疗组中,血清前列腺特异性抗原水平在30周后略有上升,在开始的12个月中没有进一步上升,保持稳定在正常范围内。在随后的TU注射之前的血浆T高于参考值的下限。每年进行四次注射就足够了。结论:每12周一次TU的治疗对于性腺功能减退的男性至少与TE一样安全和有效,而且给药频率要低得多。当所有受试者均接受TU治疗后,超过114周的随访结果显示出极好的疗效和安全性。

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