Endocrinology and Metabolic Diseases, University of Bari Aldo Moro, Foggia, Italy.
Curr Pharm Des. 2011;17(15):1500-11. doi: 10.2174/138161211796197160.
Until the 2000s Testosterone (T) Replacement Therapy (TRT) wasn't very satisfactory for male hypogonadic patients because the available T formulations weren't able to reproduce the physiological pattern of T secretion in man. In fact, oral formulations (oral undecanoate T) showed very short half-life (<24 hours), requiring the administration of several daily doses, whereas the old injection products (T esters) were characterized by very long half-life (>7 days) because of their adipose tissue storage, requiring to be administered every 2-3 weeks but determining remarkable and quick fluctuations (in 2-3 weeks) of the testosteronemia with variations in a few days from over-physiological levels (> 2000 ng/dl) to very low levels (< 200 ng/dl). Nowadays, several compounds can attain the standards of suitability and effectiveness of TRT in hypogonadal men. Both transcutaneous (gel) T and long-acting injectable formulations are the most modern preparations that can satisfy the criteria of an ideal chronic replacement therapy. In fact, they keep the serum T levels in the physiological range imitating its circadian rhythm, leading to the development and/or the preservation of male sexual characteristics and, finally, positively influencing bone mass, skeletal muscle and adipose tissue distribution. In particular, the availability and use of long-acting injectable undecanoate T can really improve the patients' compliance as requested for a life-long treatment. However, definitive and conclusive evidence regarding the main end-points, such as the diminished recurrence of falls in elderly men, the decrease in fractures in osteoporotic subjects, the reduction in disabling conditions and the extension of life, have not been reached so far. Therefore, the aim of this review is to sum up the most important evidence that has been collected regarding TRT, highlighting in particular those concerning both transcutaneous and long-acting injectable T compounds.
直到 21 世纪,睾酮(T)替代疗法(TRT)对男性性腺功能减退症患者并不十分满意,因为现有的 T 制剂无法复制男性 T 分泌的生理模式。事实上,口服制剂(口服十一酸睾酮)半衰期非常短(<24 小时),需要每天服用几次,而旧的注射产品(T 酯)半衰期非常长(>7 天),因为它们在脂肪组织中储存,需要每 2-3 周注射一次,但会导致睾酮血症明显且快速波动(在 2-3 周内),几天内从高于生理水平(>2000ng/dl)降至非常低水平(<200ng/dl)。如今,几种化合物可以达到男性性腺功能减退症 TRT 的适宜性和有效性标准。经皮(凝胶)T 和长效注射制剂是最现代的制剂,可以满足理想慢性替代治疗的标准。事实上,它们可以将血清 T 水平保持在生理范围内,模拟其昼夜节律,从而导致男性性特征的发展和/或维持,最终对骨量、骨骼肌和脂肪组织分布产生积极影响。特别是,长效注射用十一酸睾酮的可用性和使用可以真正提高患者对终生治疗的依从性。然而,关于主要终点(如老年男性跌倒复发减少、骨质疏松症患者骨折减少、失能状况减少和寿命延长)的明确和确凿证据尚未达到。因此,本综述的目的是总结已经收集到的关于 TRT 的最重要证据,特别是那些关于经皮和长效注射 T 化合物的证据。