Woods Gina N, Huang Mei-Hua, Cawthon Peggy M, Laughlin Gail A, Schousboe John T, McDaniels-Davidson Corinne, Cauley Jane A, Orwoll Eric, Barrett-Connor Elizabeth, Kado Deborah M
University of California, San Diego, La Jolla, CA, USA.
David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
J Bone Miner Res. 2016 Dec;31(12):2123-2128. doi: 10.1002/jbmr.2901. Epub 2016 Nov 3.
Accentuated kyphosis is associated with adverse health outcomes, including falls and fractures. Low bone density is a risk factor for hyperkyphosis, and each vertebral fracture adds roughly 4° to forward spine curvature. Sex steroids, in particular low bioavailable estradiol and high sex hormone-binding globulin (SHBG), are associated with bone loss and high SHBG is associated with vertebral fractures in older men. We, therefore, hypothesized that low bioavailable estradiol and high SHBG would be associated with worse kyphosis. To test this hypothesis, we examined the cross-sectional associations between individual bioavailable sex hormones and SHBG with radiographically assessed kyphosis. Participants included 1500 men aged 65 and older from the Osteoporotic Fractures in Men (MrOS) Study, in whom baseline measures of kyphosis and sex hormones were available. Modified Cobb angle of kyphosis, calculated from T4 through T12, was assessed from supine lateral spine radiographs. Serum total estradiol and total testosterone were measured by mass spectrometry, and bioavailable sex steroids were calculated from mass action equations. After adjustment for age and other confounding variables, no association was found between bioavailable estradiol or testosterone and Cobb angle, either when kyphosis was analyzed as a continuous variable or dichotomized into highest versus lower three quartiles. In linear regression models adjusted for age and clinic site, there was a significant association between SHBG and kyphosis (parameter estimate = 0.76 per SD increase, p = 0.01). In the fully adjusted model, this association was weakened and of only borderline statistical significance (parameter estimate = 0.61 per SD, p = 0.05). Logistic models demonstrated similar findings. Although associated with bone loss, we did not demonstrate that low bioavailable estradiol translates into worse kyphosis in older men. High SHBG is associated with bone loss and vertebral fractures. Our results suggest that high SHBG may also be a risk factor for hyperkyphosis. © 2016 American Society for Bone and Mineral Research.
脊柱后凸加重与不良健康后果相关,包括跌倒和骨折。低骨密度是脊柱后凸过度的一个危险因素,每发生一次椎体骨折会使脊柱前凸曲率增加约4°。性类固醇,特别是生物可利用雌二醇水平低和性激素结合球蛋白(SHBG)水平高,与骨质流失有关,而高SHBG与老年男性的椎体骨折有关。因此,我们推测生物可利用雌二醇水平低和SHBG水平高会与更严重的脊柱后凸相关。为了验证这一假设,我们研究了个体生物可利用性激素和SHBG与通过影像学评估的脊柱后凸之间的横断面关联。参与者包括来自男性骨质疏松性骨折(MrOS)研究的1500名65岁及以上的男性,他们有脊柱后凸和性激素的基线测量数据。从仰卧位脊柱侧位X线片评估从T4至T12计算得出的改良Cobb角脊柱后凸。通过质谱法测量血清总雌二醇和总睾酮,并根据质量作用方程计算生物可利用性类固醇。在调整年龄和其他混杂变量后,无论是将脊柱后凸作为连续变量分析还是分为最高与较低的三个四分位数时,均未发现生物可利用雌二醇或睾酮与Cobb角之间存在关联。在调整年龄和临床地点的线性回归模型中,SHBG与脊柱后凸之间存在显著关联(标准差每增加1,参数估计值 = 0.76,p = 0.01)。在完全调整模型中,这种关联减弱且仅具有临界统计学意义(标准差每增加1,参数估计值 = 0.61,p = 0.05)。逻辑模型显示了类似的结果。虽然与骨质流失有关,但我们并未证实老年男性生物可利用雌二醇水平低会导致更严重的脊柱后凸。高SHBG与骨质流失和椎体骨折有关。我们的结果表明,高SHBG也可能是脊柱后凸过度的一个危险因素。© 2016美国骨与矿物质研究学会。