Circulating Sex Steroids, Sex Hormone-Binding Globulin, and Longitudinal Changes in Forearm Bone Mineral Density in Postmenopausal Women and Men: The Tromsø Study

被引:0
作者
Åshild Bjørnerem
Nina Emaus
Gro K. R. Berntsen
Ragnar M. Joakimsen
Vinjar Fønnebø
Tom Wilsgaard
Pål Øian
Ego Seeman
Bjørn Straume
机构
[1] University of Tromsø,Institute of Community Medicine
[2] University of Tromsø,Institute of Clinical Medicine
[3] University Hospital of North Norway,Department of Medicine
[4] University Hospital of North Norway,Department of Obstetrics and Gynecology
[5] University of Melbourne,Departments of Medicine and Endocrinology, Austin Health
来源
Calcified Tissue International | 2007年 / 81卷
关键词
Bone mineral density; Longitudinal study; Population-based; Sex hormone-binding globulin; Sex steroid;
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摘要
Bone loss during advancing age in women and men is partly the result of sex steroid deficiency. As the contribution of circulating sex steroids and sex hormone-binding globulin (SHBG) to bone loss remains uncertain, we sought to determine whether levels of sex steroids or SHBG predict change in bone mineral density (BMD) in women and men. A population-based study in the city of Tromsø of 6.5 years’ duration (range 5.4-7.4) included 927 postmenopausal women aged 37–80 years and 894 men aged 25–80 years. Total estradiol and testosterone, calculated free levels, and SHBG were measured at baseline, and BMD change at the distal forearm was determined using BMD measurements in 1994–1995 and 2001. Bone loss was detected in postmenopausal women and men. Free estradiol and SHBG predicted age-adjusted bone loss in postmenopausal women, but only free estradiol was associated after further adjustment for body mass index and smoking in mixed models (P < 0.05). After same adjustment, only SHBG persisted as a significant independent predictor of bone loss in men (P < 0.001). However, only 1% of the variance in bone loss was accounted for by these measurements. We therefore conclude that the relations between sex steroids and bone loss are weak and measurements of sex steroids are unlikely to assist in clinical decision making.
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页码:65 / 72
页数:7
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共 227 条
[21]  
Klee GG(2004)Endogenous sex hormones in relation to age, sex, lifestyle factors, and chronic diseases in a general population: the Tromsø Study J Clin Endocrinol Metab 89 6039-6047
[22]  
Riggs BL(2003)The associations of age, lifestyle factors and chronic disease with testosterone in men: the Tromsø Study Eur J Endocrinol 149 145-152
[23]  
Khosla S(1989)The Tromsø Heart Study: family approach to intervention on CHD. Feasibility of risk factor reduction in high-risk persons – project description Scand J Soc Med 17 109-119
[24]  
Melton LJ(2005)Bone mineral density measures in longitudinal studies: the choice of phantom is crucial for quality assessment. The Tromsø Study, a population-based study Osteoporos Int 16 1597-1603
[25]  
Atkinson EJ(2006)Longitudinal changes in forearm bone mineral density in women and men aged 45-84 years: the Tromsø Study, a population-based study Am J Epidemiol 163 441-449
[26]  
O’Fallon WM(2005)Longitudinal changes in forearm bone mineral density in women and men aged 25–44 years: the Tromsø Study: a population-based study Am J Epidemiol 162 633-643
[27]  
Khosla S(2000)The Tromsø Study: determinants of precision in bone densitometry J Clin Epidemiol 53 1104-1112
[28]  
Melton LJ(1999)A critical evaluation of simple methods for the estimation of free testosterone in serum J Clin Endocrinol Metab 84 3666-3672
[29]  
Robb RA(2000)Relative contributions of testosterone and estrogen in regulating bone resorption and formation in normal elderly men J Clin Invest 106 1553-1560
[30]  
Camp JJ(2001)Sex steroids and bone Physiol Rev 81 419-447