Vold Jørn Henrik, Vogt Elinor Chelsom, Heldal Anne Taraldsen, Chalabianloo Fatemeh, Druckrey-Fiskaaen Karl Trygve, Løberg Else-Marie, Methlie Paal, Johansson Kjell Arne, Fadnes Lars Thore
Department of Addiction Medicine, Haukeland University Hospital, Bergen N-5021, Norway.
Department of Global Public Health and Primary Care, University of Bergen, Bergen N-5020, Norway.
J Endocr Soc. 2025 Jun 28;9(9):bvaf114. doi: 10.1210/jendso/bvaf114. eCollection 2025 Sep.
Low testosterone levels are often considered an adverse effect of chronic opioid use. However, the prevalence of low testosterone levels and the association between testosterone levels and clinical symptoms among males receiving opioid agonist therapy (OAT) remain unclear.
To biochemically investigate the prevalence of low testosterone levels (free testosterone ≤0.22 nmol/L) and the association between free testosterone levels and symptoms of fatigue, measured using the 3-item Fatigue Severity scale, and psychological distress, measured using the 10-item Hopkins Symptoms Checklist.
Prospective cohort study based on data collected between May 2017 and May 2024 from males receiving OAT recruited from OAT clinics at Haukeland University Hospital, Bergen, Norway.
295 males aged 23 to 71 years, with a mean OAT duration of 8 years.
A total of 236 (80%) of participants had low testosterone levels at baseline, and 108/148 (73%) had low testosterone levels in 2 consecutive measurements. No association was found between free testosterone and fatigue (baseline: coefficient: -1.0, 95% confidence interval: -6.4; 4.5, Δscore/year: 0.8, -5.2; 6.8) or between free testosterone and psychological distress (baseline: 0.4, -0.3; 1.0, Δscore/year: -0.1, -0.3; 0.2).
Eighty percent of males receiving OAT had low testosterone levels. However, testosterone levels were not associated with symptoms of fatigue or psychological distress. These findings should be interpreted with caution due to suboptimal power and potential influence of confounding. Further research is warranted to clarify the clinical significance of biochemical threshold values for low testosterone levels and their relationship to specific clinical symptoms in the OAT population.
低睾酮水平常被认为是慢性阿片类药物使用的不良反应。然而,接受阿片类激动剂治疗(OAT)的男性中低睾酮水平的患病率以及睾酮水平与临床症状之间的关联仍不明确。
通过生化方法调查低睾酮水平(游离睾酮≤0.22 nmol/L)的患病率,以及使用3项疲劳严重程度量表测量的游离睾酮水平与疲劳症状之间的关联,和使用10项霍普金斯症状清单测量的心理困扰之间的关联。
前瞻性队列研究,基于2017年5月至2024年5月期间从挪威卑尔根豪克兰大学医院的OAT诊所招募的接受OAT治疗的男性收集的数据。
295名年龄在23至71岁之间的男性,平均OAT治疗时长为8年。
共有236名(80%)参与者在基线时睾酮水平较低,108/148名(73%)在连续两次测量中睾酮水平较低。未发现游离睾酮与疲劳之间存在关联(基线:系数:-1.0,95%置信区间:-6.4;4.5,每年变化得分:0.8,-5.2;6.8),也未发现游离睾酮与心理困扰之间存在关联(基线:0.4,-0.3;1.0,每年变化得分:-0.1,-0.3;0.2)。
80%接受OAT治疗的男性睾酮水平较低。然而,睾酮水平与疲劳症状或心理困扰无关。由于效能欠佳和混杂因素的潜在影响,这些发现应谨慎解读。有必要进一步研究以阐明低睾酮水平生化阈值的临床意义及其与OAT人群特定临床症状的关系。