van Os Joël, Smit Diederik Laurens, Bond Peter, de Ronde Willem
Spaarne Gasthuis, Department of Internal Medicine, Haarlem, Netherlands.
Android Health Clinic, Department of Performance and Image-enhancing Drugs Research, Utrecht, Netherlands.
Front Endocrinol (Lausanne). 2025 Jul 3;16:1621558. doi: 10.3389/fendo.2025.1621558. eCollection 2025.
Androgen abuse, which is increasingly prevalent, inevitably leads to suppression of the hypothalamic-pituitary-gonadal axis (HPGA). While most individuals recover HPGA function following androgen cessation, a subset experiences prolonged hypogonadism, with symptoms persisting for months or even years. Currently, this condition lacks a standardized definition, complicating both diagnosis and treatment. In this article, we explore the potential mechanisms underlying prolonged hypogonadism after androgen abuse, including the role of prolonged androgen activity, hypothalamic-pituitary alterations, testicular changes, suppression of sex hormone-binding globulin (SHBG), genetic predisposition, and undisclosed ongoing androgen abuse. We propose the term 'Prolonged Post-Androgen Abuse Hypogonadism'(PPAAH) to standardize diagnosis and guide future research. PPAAH is provisionally defined as persistent hypogonadism six months after cessation of androgen abuse, in individuals with a cumulative androgen exposure of at least 150 mg per week for a minimum of six months. Diagnosing PPAAH requires excluding other causes of hypogonadism. This preliminary framework is intended to support further research into the pathophysiology and management of this condition, and may require refinement as further evidence emerges.
雄激素滥用现象日益普遍,不可避免地会导致下丘脑 - 垂体 - 性腺轴(HPGA)受到抑制。虽然大多数人在停止使用雄激素后HPGA功能会恢复,但有一部分人会出现性腺功能减退持续时间延长的情况,症状会持续数月甚至数年。目前,这种情况缺乏标准化定义,给诊断和治疗都带来了困难。在本文中,我们探讨了雄激素滥用后性腺功能减退持续时间延长的潜在机制,包括雄激素活性持续时间、下丘脑 - 垂体改变、睾丸变化、性激素结合球蛋白(SHBG)抑制、遗传易感性以及未公开的持续雄激素滥用的作用。我们提出了“雄激素滥用后性腺功能减退持续时间延长”(PPAAH)这一术语,以规范诊断并指导未来的研究。PPAAH暂定义为在雄激素滥用停止六个月后仍持续存在性腺功能减退,且每周累计雄激素暴露量至少为150毫克,持续时间至少为六个月的个体。诊断PPAAH需要排除性腺功能减退的其他原因。这个初步框架旨在支持对这种情况的病理生理学和管理的进一步研究,并且可能需要随着更多证据的出现而进行完善。