Age-related changes in cortical bone content of insulin-like growth factor binding protein (IGFBP)-3, IGFBP-5, osteoprotegerin, and calcium in postmenopausal osteoporosis: A cross-sectional study

被引:47
作者
Ueland, T [1 ]
Brixen, K
Mosekilde, L
Mosekilde, L
Flyvbjerg, A
Bollerslev, J
机构
[1] Univ Oslo, Natl Hosp, Dept Endocrinol, N-0027 Oslo, Norway
[2] Univ Oslo, Natl Hosp, Internal Med Res Inst, N-0027 Oslo, Norway
[3] Aarhus Univ Hosp, Dept Endocrinol C, DK-8000 Aarhus, Denmark
[4] Univ Aarhus, Dept Cell Biol, DK-8000 Aarhus, Denmark
[5] Odense Univ Hosp, Dept Endocrinol, DK-5000 Odense, Denmark
[6] Aarhus Univ Hosp, Med Res Labs, DK-8000 Aarhus, Denmark
关键词
D O I
10.1210/jc.2002-020977
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Serum GH and IGF-I levels decline with increasing age, whereas osteoprotegerin (OPG) increases. IGFs as well as OPG are present in bone matrix and mediate the effects of many upstream hormones (e.g. estrogen). To evaluate whether changes in these proteins may to some extent explain the decrease in bone mass in postmenopausal or senile osteoporosis, we measured bone contents of IGF-I, IGF-II, IGF binding protein (IGFBP)-3, IGFBP-5, and OPG in combined extracts obtained after EDTA and guanidine hydrochloride extraction in 60 postmenopausal women aged 47-74 (mean, 63) yr with a previous distal forearm fracture and a hip or spine Z-score less than 0. We found age-related increases in IGFBP-3 (r = 0.35; P < 0.01), IGFBP-5 (r = 0.59; P < 0.001), and OPG (r = 0.36; P < 0.01) in cortical bone, significantly inversely correlated with femoral neck and lumbar spine BMD. A correlation between age and OPG was also detected in trabecular bone (r = 0.27; P < 0.05). A pronounced age-related decrease in cortical calcium contents (r = -0.60; P < 0.001), positively correlated with femoral neck and lumbar spine BMD, was also found. No age-related changes were detected for IGF-I or IGF-II. The present study demonstrates age-related changes in cortical bone contents of IGFBPs, calcium, and OPG, possibly related to the pathophysiology of postmenopausal osteoporosis. As for OPG, our findings probably represent compensatory responses to increased osteoclastic resorption.
引用
收藏
页码:1014 / 1018
页数:5
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