首页> 美国卫生研究院文献>Journal of Bone and Mineral Research >The limited clinical utility of testosterone estradiol and sex hormone binding globulin measurements in the prediction of fracture risk and bone loss in older men
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The limited clinical utility of testosterone estradiol and sex hormone binding globulin measurements in the prediction of fracture risk and bone loss in older men

机译:睾丸激素雌二醇和性激素结合球蛋白测定在预测老年男性骨折风险和骨质流失方面的临床应用有限

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摘要

Measurement of serum testosterone (T) levels is recommended in the evaluation of osteoporosis in older men and estradiol (E2) and sex hormone binding globulin (SHBG) levels are associated with the rate of bone loss and fractures, but the clinical utility of sex steroid and SHBG measurements for the evaluation of osteoporosis in men has not been examined. To evaluate whether measurements of T, E2 and/or SHBG are useful for the prediction of fracture risk or the rate of bone loss in older men, we analyzed longitudinal data from 5487 community-based men participating in the MrOS Study in the US, Sweden and Hong Kong. Serum T, E2 and SHBG levels were assessed at baseline; incident fractures were self-reported at 4 month intervals with radiographic verification (US), or ascertained via national health records (Sweden, Hong Kong). Rate of bone loss was assessed by serial measures of hip BMD. We used receiver operating characteristic (ROC) curves, net reclassification improvement (NRI) and integrated discrimination improvement (IDI) to assess improvement in prediction. Mean age at baseline was 72-75 years and the prevalence of low T levels (<300 ng/dL) was 7.6-21.3% in the three cohorts. There were 619 incident major osteoporotic and 266 hip fractures during follow up of approximately 10 years. Based on ROC curves, there were no improvements in fracture risk discrimination for any biochemical measure when added to models, including FRAX with BMD. Although minor improvements in NRI were observed for the dichotomous parameters low BioE2 (<11.4 pg/ml) and high SHBG (>59.1 nM), neither sex steroids nor SHBG provided clinically useful improvement in fracture risk discrimination. Similarly, they did not contribute to the prediction of BMD change. In conclusion, there is limited clinical utility of serum E2, T and SHBG measures for the evaluation of osteoporosis risk in elderly men.
机译:建议在老年男性骨质疏松症的评估中测量血清睾丸激素(T)的水平,而雌二醇(E2)和性激素结合球蛋白(SHBG)的水平与骨质流失和骨折的发生率相关,但是性类固醇的临床应用尚未评估用于评估男性骨质疏松的SHBG和SHBG测量。为了评估T,E2和/或SHBG的测量值是否可用于预测老年男性的骨折风险或骨质流失率,我们分析了来自5487位社区男性的纵向数据,这些男性参与了美国,瑞典的MrOS研究。和香港。在基线时评估血清T,E2和SHBG水平;通过放射线检查(美国)每4个月进行一次自我报告的突发性骨折,或通过国家健康记录确定(瑞典,香港)。骨丢失率通过髋部BMD的一系列测量来评估。我们使用接收器工作特性(ROC)曲线,净重分类改进(NRI)和综合辨别改进(IDI)来评估预测方面的改进。在这三个队列中,基线的平均年龄为72-75岁,低T水平(<300 ng / dL)的患病率为7.6-21.3%。在大约10年的随访期间,共发生619例重大骨质疏松症和266例髋部骨折。基于ROC曲线,添加到模型(包括带有BMD的FRAX)后,对于任何生化指标,骨折风险的判别都没有改善。尽管对于二分参数,低BioE2(<11.4 pg / ml)和高SHBG(> 59.1 nM)观察到的NRI略有改善,但无论是性类固醇还是SHBG都不能在骨折风险识别方面提供临床上有用的改善。同样,它们对BMD变化的预测没有贡献。总之,血清E2,T和SHBG指标在评估老年男性骨质疏松症风险方面的临床应用有限。

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