Volume 4, Issue 2 (June 2002) 4, 117–121;
Bone mineral density in hypogonadal men remains low after long-term testosterone replacement
K. Ishizaka, M. Suzuki, Y. Kageyama, K. Kihara, K.I. Yoshida
1.Department of Urology, Kanto Central Hospital, Tokyo 158-8531, Japan 2.Department of Urology and Reproduction, Tokyo Medical and Dental University 3.Department of Urology, Dokkyo University School of Medicine
Advance online publication 1 June 2002
Abstract |
Aim: In 11 congenital hypogonadal men, the bone mineral density (BMD) values were determined to assess the effect of long-term androgen replacement therapy (ART) on skeletal integrity. Methods: Eleven congenital hypogonadal men, including 8 isolated gonadotropin deficiency patients, 2 Kallmann's syndrome and 1 vanishing testes syndrome were recruited and treated with 250 mg of testosterone enanthate intramuscularly every 4 weeks for 7-43 years (meanSD: 21.513 years). In these patients and a group of 10 healthy young men (controls), the whole and trabecular BMDs were examined at the distal end of radius by means of a peripheral quantitative computerized tomography device. Results: The whole radial BMD in hypogonadal men was significantly less in the patients than in the healthy men (498115 and 725134 mg/cm3, respectively; P<0.01); the trabecular BMD was also lower in the hypogonadal men (19980 and 37589 mg/cm3; P< 0.01). The whole radial BMD values in 10 of 11 hypogonadal men were at least 1 SD below the mean value for healthy young men; 2 hypogonadal men had BMD values more than 2.5 SD lower than the healthy mean. Additionally, the whole radial BMD showed a significant negative correlation with the patient's age at the initiation of ART (r = 0.748, P<0.01). The serum level of bone-specific alkaline phosphatase and the urinary level of deoxypyridinoline were not significantly different between the two groups. Conclusion: Osteopenia persists in the hypogonadal men after long-term ART, suggesting that such patients have a persistent defect in bone development not alleviated by androgen replacement.
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