Effects of oral testosterone undecanoate therapy on bone mineral density and body composition in 322 aging men with symptomatic testosterone deficiency: a 1-year, randomized, placebo-controlled, dose-ranging study

被引:32
作者
Bouloux, Pierre M. G. [1 ]
Legros, Jean-Jacques [2 ]
Elbers, Jolanda M. H. [3 ]
Geurts, T. B. Paul [4 ]
Kaspers, Marion J. G. H. [5 ]
Meehan, Alan G. [6 ]
Meuleman, Eric J. H. [7 ]
机构
[1] Royal Free & Univ Coll Med Sch, Ctr Neuroendocrinol, London NW3 2QG, England
[2] Univ Liege, Dept Endocrinol, Liege, Belgium
[3] Merck Sharp & Dohme Corp, Global Clin Res, Oss, Netherlands
[4] MSD Anim Hlth, Global Commun, Boxmeer, Netherlands
[5] Merck Sharp & Dohme Ltd, Global Res Data & Quantitat Sci, Oss, Netherlands
[6] Merck Sharp & Dohme Corp, Off Chief Med Officer, Whitehouse Stn, NJ USA
[7] Free Univ Amsterdam, Dept Urol, Med Ctr, Amsterdam, Netherlands
关键词
Aging males; body composition; bone mineral density; placebo; testosterone deficiency; testosterone undecanoate; LATE-ONSET HYPOGONADISM; OLDER MEN; ELDERLY-MEN; EXOGENOUS TESTOSTERONE; PHYSICAL PERFORMANCE; SERUM TESTOSTERONE; MUSCLE STRENGTH; WHOLE-BODY; YOUNG MEN; OSTEOPOROSIS;
D O I
10.3109/13685538.2013.773420
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: We investigated the effects of oral testosterone undecanoate (TU) on bone mineral density (BMD), lean body mass (LBM) and body fat mass (BFM) in aging men with symptomatic testosterone deficiency (TD). Methods: Three hundred twenty-two men >= 50 years with TD symptoms and calculated free testosterone <0.26 nmol/L participated in a multicenter, double-blind, placebo-controlled trial. Patients were randomized to placebo, oral TU 80 mg/d, oral TU 160 mg/d, or oral TU 240 mg/d, administered as divided doses with normal meals. BMD of the hip and lumbar spine were evaluated by dual energy X-ray absorptiometry (DEXA), and body composition (LBM and BFM) by whole body DEXA. Results: Oral TU significantly increased BMD at Month 12 at the lumbar spine (240 mg/d), total hip (240 mg/d), and trochanter and intertrochanter (160 and 240 mg/d) compared with placebo. Oral TU significantly increased LBM at Months 6 and 12 for all oral TU groups compared with placebo. BFM significantly decreased at Month 6 (all oral TU groups) and Month 12 (160 mg/d) compared with placebo. The effects on BMD and body composition showed a clear dose response. Conclusions: Treatment with oral TU led to improvement in BMD, LBM and BFM in aging men with symptomatic TD.
引用
收藏
页码:38 / 47
页数:10
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