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Effect of Testosterone Treatment on Volumetric Bone Density and Strength in Older Men With Low Testosterone

医学 睾酮(贴片) 定量计算机断层扫描 安慰剂 骨矿物 体质指数 泌尿科 骨质疏松症 内科学 骨密度 内分泌学 替代医学 病理
作者
Peter J. Snyder,David L. Kopperdahl,Alisa J. Stephens‐Shields,Susan S. Ellenberg,Jane A. Cauley,Kristine E. Ensrud,Cora E. Lewis,Elizabeth Barrett‐Connor,Ann V. Schwartz,Dong Hoon Lee,Shalender Bhasin,Glenn R. Cunningham,Thomas M. Gill,Alvin M. Matsumoto,Ronald S. Swerdloff,Shehzad Basaria,Susan J. Diem,Christina Wang,Xiaoling Hou,Denise Cifelli,Darlene Dougar,Bret Zeldow,Douglas C. Bauer,Tony M. Keaveny
出处
期刊:JAMA Internal Medicine [American Medical Association]
卷期号:177 (4): 471-471 被引量:239
标识
DOI:10.1001/jamainternmed.2016.9539
摘要

Importance

As men age, they experience decreased serum testosterone concentrations, decreased bone mineral density (BMD), and increased risk of fracture.

Objective

To determine whether testosterone treatment of older men with low testosterone increases volumetric BMD (vBMD) and estimated bone strength.

Design, Setting, and Participants

Placebo-controlled, double-blind trial with treatment allocation by minimization at 9 US academic medical centers of men 65 years or older with 2 testosterone concentrations averaging less than 275 ng/L participating in the Testosterone Trials from December 2011 to June 2014. The analysis was a modified intent-to-treat comparison of treatment groups by multivariable linear regression adjusted for balancing factors as required by minimization.

Interventions

Testosterone gel, adjusted to maintain the testosterone level within the normal range for young men, or placebo gel for 1 year.

Main Outcomes and Measures

Spine and hip vBMD was determined by quantitative computed tomography at baseline and 12 months. Bone strength was estimated by finite element analysis of quantitative computed tomography data. Areal BMD was assessed by dual energy x-ray absorptiometry at baseline and 12 months.

Results

There were 211 participants (mean [SD] age, 72.3 [5.9] years; 86% white; mean [SD] body mass index, 31.2 [3.4]). Testosterone treatment was associated with significantly greater increases than placebo in mean spine trabecular vBMD (7.5%; 95% CI, 4.8% to 10.3% vs 0.8%; 95% CI, −1.9% to 3.4%; treatment effect, 6.8%; 95% CI, 4.8%-8.7%;P < .001), spine peripheral vBMD, hip trabecular and peripheral vBMD, and mean estimated strength of spine trabecular bone (10.8%; 95% CI, 7.4% to 14.3% vs 2.4%; 95% CI, −1.0% to 5.7%; treatment effect, 8.5%; 95% CI, 6.0%-10.9%;P < .001), spine peripheral bone, and hip trabecular and peripheral bone. The estimated strength increases were greater in trabecular than peripheral bone and greater in the spine than hip. Testosterone treatment increased spine areal BMD but less than vBMD.

Conclusions and Relevance

Testosterone treatment for 1 year of older men with low testosterone significantly increased vBMD and estimated bone strength, more in trabecular than peripheral bone and more in the spine than hip. A larger, longer trial could determine whether this treatment also reduces fracture risk.

Trial Registration

clinicaltrials.gov Identifier: NCT00799617

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