The association between sex hormone-binding globulin gene polymorphism with bone mineral density

Steroids ◽  
2016 ◽  
Vol 106 ◽  
pp. 9-18 ◽  
Author(s):  
Xiao-Yun Zha ◽  
Yu Hu ◽  
Xiao-Na Pang ◽  
Ji-Heng Zhu ◽  
Gui-Lin Chang ◽  
...  
2002 ◽  
Vol 64 (4) ◽  
pp. 612-620 ◽  
Author(s):  
Linda D. Cameron ◽  
Howard Leventhal ◽  
Richard R. Love ◽  
Linda J. Patrick-Miller

2018 ◽  
Vol 50 (01) ◽  
pp. 65-72 ◽  
Author(s):  
Hai-Juan Liu ◽  
Jun Yan ◽  
Yan Li ◽  
Fang-Yuan Zhou ◽  
Xu-Dong Su ◽  
...  

AbstractSeveral groups have reported the important role of estradiol (E2) and testosterone (T) in postmenopausal osteoporosis (PMOP). Because aromatase catalyzes the conversion of T to E2, the purpose of this study was to determine the influence of aromatase activity on the bone mineral density (BMD) in postmenopausal women. A total of 344 postmenopausal women were selected for this study. Serum E2, T, sex hormone-binding globulin (SHBG), calcium (Ca), alkaline phosphatase (ALP), C-terminal telopeptide of type I collagen (CTX), and procollagen type I amino-terminal propeptide (PINP) were examined. The E2/T was positively associated with total hip BMD and PINP (p<0.05). When E2/T was divided into quartiles, participants in lower quartiles of E2/T were likely to have higher PINP and lower BMD (p<0.05). The prevalence of osteoporosis significantly increased as E2/T ratio decreased. The receiver operating characteristic (ROC) curves were constructed for serum E2, free E2 index (FEI), and E2/T, to assess their diagnostic accuracy in PMOP. The overall area under the curve (AUC) were 0.83 (95% CI=0.77–0.88) for E2, 0.87 (95% CI=0.82–0.92) for FEI, and 0.89 (95% CI=0.85–0.94), respectively. In conclusion, the study suggests that in postmenopausal women, aromatase activity could be an important determinant of skeletal health. The women with lower aromatase activity may have greater likelihood of PMOP and the E2/T was expected to be a valuable indicator for the prediction of PMOP and to monitor the process of osteoporosis.


2009 ◽  
Vol 10 (8) ◽  
pp. 1177-1184 ◽  
Author(s):  
Marcel E. Ooms ◽  
Paul Lips ◽  
Jan C. Roos ◽  
Wim J. F. van der Vijgh ◽  
Corrie Popp-Snijders ◽  
...  

Bone ◽  
2009 ◽  
Vol 45 (6) ◽  
pp. 1169-1174 ◽  
Author(s):  
Nicola Napoli ◽  
Ana Varadharajan ◽  
Giovam Batista Rini ◽  
Romano Del Fiacco ◽  
Jayasree Yarramaneni ◽  
...  

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Zhongxin Zhu ◽  
Jin Zhao ◽  
Yanfei Fang ◽  
Rongwei Hua

Abstract Background Changes in sex hormones are thought to play an important role in bone health in postmenopausal women. Our aim in this study was to evaluate the association between levels of estradiol (E2), which is the most potent endogenous estrogen, and sex hormone binding globulin (SHBG) and bone mineral density (BMD) among postmenopausal women, 40–59 years of age. Methods Using data from the National Health and Nutrition Examination Survey 2013–2016, we performed weighted multivariable linear regression models to evaluate the associations between serum levels of E2 and SHBG and lumbar BMD. A weighted generalized additive model and smooth curve fitting were used to address potential nonlinearity. Results A total of 608 postmenopausal women were included in the analysis. The serum E2 level was positively associated with lumbar BMD, after adjusting for other covariates (β 0.65; 95% confidence interval (CI) 0.38–0.93). An inverted U-shaped association between the serum E2 level and lumbar BMD was further identified, with the point of inflection at an E2 level of 70 pg/mL. There was no significant association between the SHBG level and lumbar BMD (β 0.01; 95% CI − 0.30 to 0.31). However, the association between these two variables was U-shaped, with the point of inflection at an SHBG level of 65 nmol/L. Conclusions Based on our findings, it may be beneficial to appropriately increase serum E2 levels to promote bone health in postmenopausal women with low estrogen levels. Considering the inverted U-shaped association, an excessive E2 level may be harmful to BMD. In addition, increasing the SHBG level to within the normal range (65–144 nmol/L) may be considered.


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