Bone loss in relation to serum levels of osteoprotegerin and nuclear factor-κB ligand: the Tromso Study

被引:27
|
作者
Jorgensen, L. [1 ,2 ]
Vik, A. [3 ]
Emaus, N. [2 ]
Brox, J. [4 ,5 ]
Hansen, J. -B. [3 ]
Mathiesen, E. [6 ,7 ]
Vestergaard, P. [8 ]
机构
[1] Univ Hosp N Norway, Div Rehabil Serv, Tromso, Norway
[2] Univ Tromso, Inst Community Med, N-9037 Tromso, Norway
[3] Univ Tromso, CART, Inst Clin Med, N-9037 Tromso, Norway
[4] Univ Tromso, Inst Med Biol, N-9037 Tromso, Norway
[5] Univ Hosp N Norway, Dept Med Biochem, Tromso, Norway
[6] Univ Tromso, Dept Neurol, Inst Clin Med, N-9037 Tromso, Norway
[7] Univ Hosp N Norway, Dept Neurol, Tromso, Norway
[8] Aarhus Kommune Hosp, Osteoporosis Clin, DK-8000 Aarhus, Denmark
关键词
Bone loss; Bone mineral density; Epidemiology; Nuclear factor-kappa B ligand; Osteoprotegerin; SOLUBLE RECEPTOR-ACTIVATOR; POSTMENOPAUSAL WOMEN; MINERAL DENSITY; CIRCULATING OSTEOPROTEGERIN; FRACTURES; AGE; OSTEOPOROSIS; POPULATION; ESTROGEN; MASS;
D O I
10.1007/s00198-009-1035-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this longitudinal study of 4,137 persons, bone mineral density was negatively associated with osteoprotegerin at baseline in both genders. In postmenopausal women not using hormone replacement therapy (HRT), bone-loss increased with increasing osteoprotegerin levels, whereas no relationship was found in men, premenopausal women, or postmenopausal women taking HRT. In a population-based study of 2,003 men and 2,134 women, the relationship between the osteoprotegerin (OPG)/factor-kappa B ligand (RANKL) system and bone mineral density (BMD) and changes in BMD was examined. Baseline measurements included height, weight, BMD of the forearm, OPG, RANKL, vitamin D, and serum parathyroid hormone (PTH) and information about lifestyle, prevalent diseases, and use of medication. BMD was remeasured at follow-up 6 years later. BMD was negatively associated with OPG at baseline in both men and women (p trend over OPG levels = 0.01 and 0.007, respectively, after adjustments for age, and other confounders). In postmenopausal women not on hormone replacement therapy, bone loss increased with increasing OPG (p = 0.005), whereas no relationship was found in men, premenopausal women, or postmenopausal women on HRT (p a parts per thousand yenaEuro parts per thousand 0.28). BMD at baseline and BMD changes were not related to RANKL levels in any of the groups (p a parts per thousand yenaEuro parts per thousand 0.14). In postmenopausal women not using HRT, bone loss associated positively with OPG. The results indicate that in women deficient in sex steroids, the OPG/RANKL system may play an important counter regulatory role in order to avoid bone loss and maintain BMD. In men and women replete in sex steroids, the OPG/RANKL system was not associated with BMD.
引用
收藏
页码:931 / 938
页数:8
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