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Title: Testosterone replacement in congenital hypogonadotropic hypogonadism maintains bone density but has only limited osteoanabolic effects. Author: Antonio L, Caerels S, Jardi F, Delaunay E, Vanderschueren D. Journal: Andrology; 2019 May; 7(3):302-306. PubMed ID: 30851011. Abstract: BACKGROUND: Congenital hypogonadotropic hypogonadism (CHH) is a rare condition characterized by complete sex steroid deficiency. Therefore, CHH is a unique human model to study the impact of long-term testosterone replacement therapy (TRT) on bone. OBJECTIVE: In this single-center retrospective observational study, we assessed the long-term impact of TRT on femoral and lumbar bone mineral density (BMD) in adult CHH men. METHODS: A total of 25 patients with CHH were included. Femoral and lumbar BMD was assessed by dual-energy X-ray absorptiometry (DEXA) and reported as T-scores. In six patients (treatment-naive group), BMD was measured before start of TRT. The other 19 (pre-treated group) had received TRT for a median duration of 7 years (range 1-41 years) before first BMD measurement. RESULTS: Age at which TRT was started ranged from 12 to 57 years old. Median time between first and last DEXA scan was 11 years (range 2-28). At the first DEXA scan, 83% and 61% of CHH patients had lumbar and femoral osteopenia/osteoporosis, respectively. In the treatment-naive group, the increase in lumbar T-score was 2.19 ± 0.13 (mean ± SEM, p < 0.01 between first and last DEXA scan) and 1.47 ± 0.29 at femoral level (p < 0.001). For the pre-treated group, the increase in lumbar and femoral T-score was 0.77 ± 0.17 (p < 0.001) and 0.19 ± 0.12 (p = 0.13), respectively. However, lumbar and femoral osteopenia/osteoporosis persisted in 61% and 48% of CHH patients even after several years of continuous TRT. Additionally, BMD clearly decreased in patients who interrupted TRT. CONCLUSION: Despite modest improvement after starting TRT, BMD remains in the osteopenic/osteoporotic range in most patients with CHH. However, prolonged TRT prevents further bone loss, both at lumbar and femoral level.[Abstract] [Full Text] [Related] [New Search]