外源性睾酮或合成代谢雄激素类固醇引起的无精子症的临床治疗指南。

Manaf Al Hashimi, Germar-Michael Pinggera, Rupin Shah, Ashok Agarwal
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摘要

摘要:无精子症,定义为射精中精子缺失,是外源性睾酮(ET)和合成代谢雄激素(AAS)使用的结果。这些药物抑制下丘脑-垂体-性腺(HPG)轴,导致睾丸内睾丸激素水平降低和精子发生受损。本文综述了无精子症的病理生理机制,并概述了恢复的治疗策略。无精子症分为睾丸前、睾丸后和睾丸后三种类型,重点是基于HPG轴抑制程度和睾丸基线功能的个性化治疗方法。关键策略包括停药和监测自发恢复,特别是对使用ET时间较短的患者。对于持续性无精子症患者,建议使用促性腺激素(人绒毛膜促性腺激素[hCG]和促卵泡激素[FSH])和选择性雌激素受体调节剂(SERMs),如枸橼酸克罗米芬,单独或联合使用。全球外源性睾酮使用的增加,包括睾酮替代疗法和AAS,强调了改善相关无精子症管理的必要性,这可能是暂时的,也可能是永久性的,这取决于个人因素和使用的睾酮类型。此外,手稿讨论了预防策略,如过渡到短效睾酮制剂或结合低剂量hCG在ET治疗期间保持生育能力。虽然管理睾酮相关无精子症的指南仍然有限,但新兴研究表明激素刺激疗法的潜在功效。然而,对于与外源性睾酮使用相关的无精子症的管理,缺乏结构良好的、可控的和长期的研究,这突出表明需要这样的研究来为循证建议提供信息。
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Clinician's guide to the management of azoospermia induced by exogenous testosterone or anabolic-androgenic steroids.

Abstract: Azoospermia, defined as the absence of sperm in the ejaculate, is a well-documented consequence of exogenous testosterone (ET) and anabolic-androgenic steroid (AAS) use. These agents suppress the hypothalamic-pituitary-gonadal (HPG) axis, leading to reduced intratesticular testosterone levels and impaired spermatogenesis. This review examines the pathophysiological mechanisms underlying azoospermia and outlines therapeutic strategies for recovery. Azoospermia is categorized into pretesticular, testicular, and post-testicular types, with a focus on personalized treatment approaches based on the degree of HPG axis suppression and baseline testicular function. Key strategies include discontinuing ET and monitoring for spontaneous recovery, particularly in patients with shorter durations of ET use. For cases of persistent azoospermia, gonadotropins (human chorionic gonadotropin [hCG] and follicle-stimulating hormone [FSH]) and selective estrogen receptor modulators (SERMs), such as clomiphene citrate, are recommended, either alone or in combination. The global increase in exogenous testosterone use, including testosterone replacement therapy and AAS, underscores the need for improved management of associated azoospermia, which can be temporary or permanent depending on individual factors and the type of testosterone used. Additionally, the manuscript discusses preventive strategies, such as transitioning to short-acting testosterone formulations or incorporating low-dose hCG to preserve fertility during ET therapy. While guidelines for managing testosterone-related azoospermia remain limited, emerging research indicates the potential efficacy of hormonal stimulation therapies. However, there is a notable lack of well-structured, controlled, and long-term studies addressing the management of azoospermia related to exogenous testosterone use, highlighting the need for such studies to inform evidence-based recommendations.

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