The impact of androgen deprivation therapy on bone mineral density in men treated for paraphilic disorder: A retrospective cohort study.
De Landtsheer. Anaïs A; Bekaert. Lieslinde L; David. Karel K; Marcq. Philippe P; Jeandarme. Inge I; Decallonne. Brigitte B; Antonio. Leen L; Vanderschueren. Dirk D
Key Findings
- Longâterm use of triptorelin (or similar ADT) leads to significant declines in lumbar and femoral bone mineral density (â0.5 Tâscore units) over ~6 years.
- Patients treated with only cyproterone acetate also showed notable bone loss, but the effect was slightly smaller than with GnRH agonist alone.
- Concurrent treatment with bisphosphonates appeared to stabilize bone density, with no statistically significant Tâscore changes during the followâup period.
Practical Outcomes
- If youâre using triptorelin or other androgenâdeprivation therapies for performance or hormonal manipulation, plan regular DXA scans (every 1â2 years) to catch bone loss early. Consider adding boneâsupporting strategiesâadequate calcium, vitamin D, resistance training, and possibly a bisphosphonateâespecially if treatment extends beyond a year. Monitoring and proactive bone health measures can mitigate the hidden risk of osteoporosis from longâterm ADT.
Summary
Men who take androgenâblocking drugs like the GnRH agonist triptorelin (often used to lower testosterone) lose bone density over several years. In this study, bone loss was about half a standard deviation at the spine and hip after roughly six years of treatment. People who also took bisphosphonate medicines did not see the same drop, suggesting those drugs can help protect bone.
Abstract
Guidelines suggest treating men with paraphilic disorder with androgen-deprivation therapy (ADT). However, little evidence is available about the long-term impact on bone loss and how to manage this adverse event. The aim of this study is to assess the impact of ADT on bone mineral density (BMD) in men treated for paraphilic disorder with the androgen receptor blocker cyproterone acetate (CPA) and/or GnRH agonist triptoreline (GnRHa) and to evaluate the effect of treatment with bisphosphonates. Baseline and follow-up dual-energy X-ray absorptiometry scan (DXA-scan) data (lumbar and femoral T-scores) were retrospectively extracted from electronic medical files of paraphilic men who received CPA and/or GnRHa. A total of 53 patients with a mean age of 39.1 years (range 17.5-74.6) were included. Lumbar (-0.39 ± 0.17, Mean ± SEM, p = 0.046), femoral neck (-0.34 ± 0.09, p = 0.002) and total femur (-0.33 ± 0.12, p = 0.014) T-scores decreased significantly in the CPA-only group (n = 13) during a mean follow-up of 6.0 ± 5.3 years. In the GnRHa group (n = 29), T-scores at all sites decreased significantly over 6.6 ± 4.4 years (lumbar: -0.55 ± 0.12, p < 0.001, femoral neck: -0.53 ± 0.09, total femur: -0.44 ± 0.09, p < 0.001). In the group, who received bisphosphonates (n = 11), no significant T-score change was observed (lumbar: -0.25 ± 0.14, p = 0.106, femoral neck -0.15 ± 0.17, p = 0.402, total femur -0.25 ± 0.14, p = 0.106) during 5.0 ± 2.8 years of follow-up. Following a mean duration of 6 years of ADT, we observed a significant decline in BMD of approximately half a standard deviation in T-score at lumbar and femoral site. Although the number of patients who received bisphosphonates was limited, this treatment seems to have a positive stabilizing effect on bone density.
Study Information
pubmed
2021
2021-12-27T00:00:00.000Z
10.1111/andr.13142
5
25