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在骨量峰值时期的男性中,性激素结合球蛋白是皮质骨状态的独立决定因素。

Sex hormone-binding globulin as an independent determinant of cortical bone status in men at the age of peak bone mass.

机构信息

Department of Endocrinology, Ghent University Hospital, De Pintelaan 185, 9K12IE, 9000 Ghent, Belgium.

出版信息

J Clin Endocrinol Metab. 2010 Apr;95(4):1579-86. doi: 10.1210/jc.2009-2189. Epub 2010 Feb 4.

DOI:10.1210/jc.2009-2189
PMID:20133463
Abstract

CONTEXT

Sex steroids are important determinants of the skeletal development, growth, and maintenance after achievement of peak bone mass. A large fraction of these hormones are bound by SHBG, and previous studies have shown that SHBG could be a determinant of bone characteristics.

OBJECTIVE

We investigated associations of serum SHBG levels with cortical and trabecular bone characteristics in young healthy men.

DESIGN AND SETTINGS

A total of 677 healthy male siblings aged 25-45 yr were recruited in a cross-sectional, population-based study.

MAIN OUTCOMES

Areal bone parameters were assessed using dual-energy x-ray absorptiometry. Cortical bone parameters at the tibia and radius and trabecular vBMD at the radius were assessed using peripheral quantitative computed tomography. Serum testosterone, estradiol, and SHBG levels were measured using immunoassays.

RESULTS

Regression models including age, height, and weight showed that SHBG levels were positively associated with bone area at the hip and the whole body, but not with areal bone mineral density (BMD). Higher SHBG levels were associated with a larger cortical bone area and periosteal and endosteal circumferences at both the tibia and the radius, whereas trabecular volumetric BMD at the radius was negatively associated with SHBG levels. Associations persisted after adjustment for (free) sex steroid levels. No associations were found with cortical volumetric BMD or cortical thickness.

CONCLUSION

In this population of healthy adult men at the age of peak bone mass, SHBG levels were positively associated with cortical bone size, independently from sex-steroid levels. This suggests a possible independent role of SHBG in the determination of adult bone size.

摘要

背景

性激素是骨骼发育、生长和达到峰值骨量后维持的重要决定因素。这些激素中有很大一部分与 SHBG 结合,先前的研究表明,SHBG 可能是骨骼特征的决定因素。

目的

我们研究了血清 SHBG 水平与年轻健康男性皮质骨和小梁骨特征的相关性。

设计和设置

在一项横断面、基于人群的研究中,共招募了 677 名年龄在 25-45 岁的健康男性兄弟姐妹。

主要结果

使用双能 X 射线吸收法评估面积骨参数。使用外周定量计算机断层扫描评估胫骨和桡骨的皮质骨参数和桡骨的小梁 vBMD。使用免疫测定法测量血清睾酮、雌二醇和 SHBG 水平。

结果

包括年龄、身高和体重在内的回归模型表明,SHBG 水平与髋部和全身的骨面积呈正相关,但与面积骨密度(BMD)无关。较高的 SHBG 水平与胫骨和桡骨的皮质骨面积以及骨膜和骨内膜周长较大相关,而桡骨的小梁体积 BMD 与 SHBG 水平呈负相关。调整(游离)性激素水平后,相关性仍然存在。与皮质体积 BMD 或皮质厚度无相关性。

结论

在达到峰值骨量的健康成年男性人群中,SHBG 水平与皮质骨大小呈正相关,与性激素水平无关。这表明 SHBG 可能在成人骨骼大小的决定中具有独立作用。

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