首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >The association of concurrent vitamin D and sex hormone deficiency with bone loss and fracture risk in older men: The osteoporotic fractures in men (MrOS) study
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The association of concurrent vitamin D and sex hormone deficiency with bone loss and fracture risk in older men: The osteoporotic fractures in men (MrOS) study

机译:老年男性同时发生维生素D和性激素缺乏与骨丢失和骨折风险的关系:男性骨质疏松性骨折(MrOS)研究

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摘要

Low 25-hydroxyvitamin D (VitD), low sex hormones (SH), and high sex hormone binding globulin (SHBG) levels are common in older men. We tested the hypothesis that combinations of low VitD, low SH, and high SHBG would have a synergistic effect on bone mineral density (BMD), bone loss, and fracture risk in older men. Participants were a random subsample of 1468 men (mean age 74 years) from the Osteoporotic Fractures in Men Study (MrOS) plus 278 MrOS men with incident nonspine fractures studied in a case-cohort design. "Abnormal" was defined as lowest quartile for VitD (<20 ng/mL), bioavailable testosterone (BioT, <163 ng/dL), and bioavailable estradiol (BioE, <11 pg/mL); and highest quartile for SHBG (>59 nM). Overall, 10% had isolated VitD deficiency; 40% had only low SH or high SHBG; 15% had both SH/SHBG and VitD abnormality; and 35% had no abnormality. Compared to men with all normal levels, those with both SH/SHBG and VitD abnormality tended to be older, more obese, and to report less physical activity. Isolated VitD deficiency, and low BioT with or without low VitD, was not significantly related to skeletal measures. The combination of VitD deficiency with low BioE and/or high SHBG was associated with significantly lower baseline BMD and higher annualized rates of hip bone loss than SH abnormalities alone or no abnormality. Compared to men with all normal levels, the multivariate-adjusted hazard ratio (95% confidence interval [CI]) for incident nonspine fracture during 4.6-year median follow-up was 1.2 (0.8-1.8) for low VitD alone; 1.3 (0.9-1.9) for low BioE and/or high SHBG alone; and 1.6 (1.1-2.5) for low BioE/high SHBG plus low VitD. In summary, adverse skeletal effects of low sex steroid levels were more pronounced in older men with low VitD levels. The presence of low VitD in the presence of low BioE/high SHBG may contribute substantially to poor skeletal health.
机译:低25-羟基维生素D(VitD),低性激素(SH)和高性激素结合球蛋白(SHBG)水平在老年男性中很常见。我们测试了以下假设:低VitD,低SH和高SHBG的组合对老年男性的骨矿物质密度(BMD),骨质流失和骨折风险具有协同作用。参与者是来自男性骨质疏松性骨折研究(MrOS)的1468名男性(平均年龄74岁)的随机子样本,以及在病例队列设计中研究的278例非脊柱骨折的MrOS男性。 “异常”定义为VitD(<20 ng / mL),生物利用睾丸激素(BioT,<163 ng / dL)和生物利用雌二醇(BioE,<11 pg / mL)的最低四分位数; SHBG的最高四分位数(> 59 nM)。总体而言,有10%的人患有孤立的VitD缺乏症; 40%的人只有低SH或高SHBG; 15%的人同时患有SH / SHBG和VitD异常; 35%没有异常。与所有正常水平的男性相比,SH / SHBG和VitD异常的男性倾向于年龄更大,更肥胖,并且身体活动较少。孤立的VitD缺乏症,以及低或无VitD的BioT均与骨骼测量无明显关系。与单独的SH异常或无异常相比,VitD缺乏症与低BioE和/或高SHBG的组合与基线BMD显着降低和髋骨丢失年化率更高相关。与所有正常水平的男性相比,在4.6年的中位随访期间,仅低VitD发生的多发非脊柱骨折的多因素校正风险比(95%置信区间[CI])为1.2(0.8-1.8);仅针对较低的BioE和/或较高的SHBG为1.3(0.9-1.9);较低的BioE /较高的SHBG和较低的VitD为1.6(1.1-2.5)。总之,在低VitD水平的老年男性中,性激素水平低对骨骼的不利影响更为明显。在低BioE /高SHBG的情况下,低VitD的存在可能会严重影响骨骼健康。

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