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[Effect of immunosuppression-induced hypogonadism on bone metabolism after heart transplantation]
1Medizinische Poliklinik Innenstadt, Ludwig Maximilians Universität München.
Insights
Cardiac transplant recipients have a high incidence of hypogonadism, leading to significant bone loss. Testosterone replacement therapy did not significantly improve bone mineral density in these patients.
Area of Science:
- Endocrinology
- Transplantation Medicine
- Bone Metabolism
Background:
- Accelerated bone loss is a known complication following cardiac transplantation (HTx).
- The impact of immunosuppression-induced hypogonadism on bone health post-HTx requires further definition.
- Osteoporosis is a common consequence of hypogonadism in men.
Purpose of the Study:
- To determine the incidence of hypogonadism in male cardiac transplant recipients.
- To investigate the influence of hypogonadism on bone mineral metabolism after HTx.
- To evaluate the efficacy of testosterone replacement therapy in hypogonadal transplant patients.
Main Methods:
- 88 male cardiac transplant recipients were randomized into normogonadal and hypogonadal groups based on hormonal status.
- Bone mineral density (BMD) at the lumbar spine was measured using DEXA at baseline and after 1 and 2 years.
- Hypogonadal patients received testosterone supplementation in addition to standard calcium and vitamin D therapy.
Main Results:
- A significant prevalence of hypogonadism (24%) was observed in male cardiac transplant recipients, independent of age.
- Hypogonadal patients exhibited significantly lower BMD compared to normogonadal patients (p < 0.001).
- Testosterone replacement therapy did not lead to a significant increase in BMD in hypogonadal patients over the 2-year follow-up period.
Conclusions:
- Hypogonadism is highly prevalent (approx. 25%) in male cardiac transplant recipients across all age groups.
- Hypogonadism significantly contributes to bone loss in this patient population.
- Testosterone substitution therapy showed no significant benefit in increasing BMD in hypogonadal cardiac transplant recipients.
Background And Objective:
Accelerated bone loss is a well recognized complication after cardiac transplantation (HTx). The role of an immunosuppressive-induced hypogonadism, a well-known cause of osteoporosis in men and its prevention are less defined after HTx. The aim of this study was first, to evaluate the incidence of hypogonadism after HTx and its influence on bone mineral metabolism and second, to assess the effect of a testosterone replacement therapy in hypogonadal transplants.
Patients And Methods:
Due to hormonal status, 88 male cardiac transplants were randomised to a normogonadal or hypogonadal group. At baseline as well as after 1 and 2 years bone mineral density (BMD g/cm (2), T-score) was measured at the lumbar spine with DEXA. All patients received a basic therapy of calcium and vitamin D. The hypogonadal patients received additional testosterone.
Results:
21 patients (24 %) showed an age-independent hypogonadism. Hypogonadal transplants showed a significant lower BMD (p < 0.001) (BMD = 0.8070 g/cm (2), T-value = -2.6514) than normogonadal patients (BMD = 0.9882 g/cm (2), T-value = -1.0568). Despite testosterone replacement hypogonadal patients showed no significant additional increase in BMD over 1 - 2 years compared with the normogonadal.
Conclusion:
Male cardiac transplants in all age groups show an high prevalence of hypogonadism (approximately 25 %) which contributes to a significant bone loss. An additional testosterone substitution did not significantly increase BMD.
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