Andrologia · 2010 · 13 citations · 39 references
MedicineEndocrinologyPharmacotherapyAndrologyParenteral Dosage FormsReproductive EndocrinologyAndrogen DeficiencyAndrogen TherapyProstate DisordersProstate-specific Antigen TestingTesticular FunctionTesticular PhysiologyAge-related Androgen DeclineAging-related Androgen DeclineAndrogen PharmacologyInternational Prostate Symptom ScoreProstate Volume MeasurementProstate-specific Antigen KineticsSerum Testosterone MeasurementTestosterone Therapy
This study investigated the safety of administration of long-acting parenteral testosterone undecanoate (TU) to 122 hypogonadal, mainly elderly men, aged 59.6 ± 8.0 years (range 18-83 years old), with baseline testosterone levels between 5.8 and 12.1 nmol l(-1) (mean ± SD = 9.3 ± 1.7). Patients were followed for 24 months. Plasma testosterone rose from 9.3 ± 1.7 to 14.9 ± 4.5 nmol l(-1) (P< 0.01) at 3 months, then stabilised at 19.2 ± 4.6 nmol l(-1) after 6 months. International Prostate Symptoms Scores and Residual Bladder Volumes decreased significantly (P <0.01) over the study period. Prostate volume and prostate-specific antigen levels fluctuated over the study period but had not increased significantly after 24 month. Haemoglobin concentrations increased significantly (P < 0.001) over the 24 months while the haematocrit increased significantly (P < 0.001) during the first 15 months and then levelled off. Statistical analysis with expressing values as means ± SD masks excesses above reference values of individual patients. These excesses were noted in low numbers, were permanently present in some but not in other individuals, and did not increase in number over the 24 month study period. Over 24 months treatment with TU appeared acceptably safe, but longer and larger scale studies are needed.
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