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Androgen replacement therapy : present and future.

机译:雄激素替代疗法:现在和将来。

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摘要

The major goal of androgen substitution is to replace testosterone at levels as close to physiological levels as is possible. For some androgen-dependent functions testosterone is a pro-hormone, peripherally converted to 5alpha-dihydrotestosterone (DHT) and 17beta-estradiol (E(2)), of which the levels preferably should be within normal physiological ranges. Furthermore, androgens should have a good safety profile without adverse effects on the prostate, serum lipids, liver or respiratory function, and they must be convenient to use and patient-friendly, with a relative independence from medical services.Natural testosterone is viewed as the best androgen for substitution in hypogonadal men. The reason behind the selection is that testosterone can be converted to DHT and E(2), thus developing the full spectrum of testosterone activities in long-term substitution.The mainstays of testosterone substitution are parenteral testosterone esters (testosterone enantate and testosterone cipionate) administered every 2-3 weeks. A major disadvantage is the strongly fluctuating levels of plasma testosterone, which are not in the physiological range at least 50% of the time. Also, the generated plasma E(2) is usually supraphysiological. A major improvement is parenteral testosterone undecanoate producing normal plasma levels of testosterone for 12 weeks, with normal plasma levels of DHT and E(2) also. Subcutaneous testosterone implants provide the patient, depending on the dose of implants, with normal plasma testosterone for 3-6 months. However, their use is not widespread. Oral testosterone undecanoate dissolved in castor oil bypasses the liver via its lymphatic absorption. At a dosage of 80mg twice daily, plasma testosterone levels are largely in the normal range, but plasma DHT tends to be elevated. For two decades transdermal testosterone preparations have been available and have an attractive pharmacokinetic profile. Scrotal testosterone patches generate supraphysiological plasma DHT levels, which is not the casewith the nonscrotal testosterone patches. Transdermal testosterone gel produces fewer skin irritations than the patches and offers greater flexibility in dosage. Oromucosal testosterone preparations have recently become available.Testosterone replacement is usually of long duration and so patient compliance is of utmost importance. Therefore, the patient must be involved in the selection of type of testosterone preparation.Administration of testosterone to young individuals has almost no adverse effects. With increasing age the risk of adverse effects on the prostate, the cardiovascular system and erythropoiesis increases. Consequently, short-acting testosterone preparations are better suited for aging androgen-deficient men.
机译:雄激素替代的主要目标是以尽可能接近生理水平的水平替代睾丸激素。对于某些雄激素依赖性功能,睾丸激素是一种激素原,可以外周转化为5α-二氢睾丸激素(DHT)和17β-雌二醇(E(2)),其水平最好应在正常的生理范围内。此外,雄激素应具有良好的安全性,而不会对前列腺,血脂,肝或呼吸功能产生不良影响,并且它们必须易于使用且对患者友好,并且与医疗服务相对独立。性腺功能减退的最佳雄激素替代品。选择它的原因是睾丸激素可以转化为DHT和E(2),从而在长期替代中发展出全方位的睾丸激素活性。睾丸激素替代的主要成分是肠胃外睾丸激素酯(对映体睾丸酮和对立睾丸酮)。每2-3周一次。一个主要的缺点是血浆睾丸激素的水平剧烈波动,至少在50%的时间内不在生理范围内。同样,生成的血浆E(2)通常是超生理的。主要的改善是肠胃外十一酸睾丸激素产生正常血浆水平的睾丸激素持续12周,而DHT和E(2)的血浆水平也正常。皮下睾丸激素植入物根据植入物的剂量为患者提供3-6个月的正常血浆睾丸激素。但是,它们的使用并不广泛。溶解在蓖麻油中的十一酸睾丸激素口服液通过其淋巴吸收绕过肝脏。每天两次服用80mg的剂量,血浆睾丸激素水平基本在正常范围内,但血浆DHT倾向于升高。二十年来,经皮睾丸激素制剂已经上市,并且具有有吸引力的药代动力学特征。阴囊睾丸激素补丁产生超生理血浆DHT水平,非阴囊睾丸激素补丁则不是这种情况。透皮睾丸激素凝胶比贴剂产生更少的皮肤刺激,并提供更大的剂量灵活性。口腔粘膜睾丸激素制剂最近已面市。睾丸激素替代通常持续时间长,因此患者依从性至关重要。因此,患者必须参与选择睾丸激素制剂的类型。对年轻人施用睾丸激素几乎没有不良影响。随着年龄的增长,对前列腺,心血管系统和红细胞生成产生不利影响的风险增加。因此,短效睾丸激素制剂更适合衰老的雄激素缺乏的男性。

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