CIRCULATING INSULIN LEVELS ARE RELATED TO BONE-DENSITY IN NORMAL POSTMENOPAUSAL WOMEN

被引:120
作者
REID, IR
EVANS, MC
COOPER, GJS
AMES, RW
STAPLETON, J
机构
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1993年 / 265卷 / 04期
关键词
OSTEOPOROSIS; BODY COMPOSITION; OBESITY;
D O I
10.1152/ajpendo.1993.265.4.E655
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We recently established that the dependence of bone mineral density (BMD) on body weight in women is mainly attributable to a close relationship between total body fat mass and BMD. The present study assesses whether this latter relationship might be contributed to by the hormones insulin or amylin, both of which may influence fat mass and calcium metabolism. Fifty-three normal postmenopausal women underwent a 75-g1 glucose tolerance test with measurement of plasma insulin and amylin concentrations every 30 min for 2 h. Body composition and BMD/height (to provide a quantity with the dimensions of volumetric density that is independent of body size) were measured by dual-energy X-ray absorptiometry, and volumetric density of the third lumbar vertebral body was calculated. Circulating insulin concentrations correlated with BMD/height and volumetric density of the third lumbar vertebral body (r = 0.28-0.52). They also were related to body weight (r = 0.34-0.56) and fat mass (r = 0.38-0.56) but were not independently related to lean mass on multiple regression. There were no consistent relationships between amylin levels and these variables. Multiple-regression analyses with fat mass and insulin levels as independent variables indicated that BMD/height of total body and femoral trochanter were primarily related to fat mass, whereas, in femoral neck, the significant relationship was with insulin. Volumetric density of the third lumbar vertebral body was related to insulin levels alone on this analysis. It is concluded that circulating insulin levels are consistently related to bone density throughout the skeleton and that this may be mediated by direct anabolic effects of insulin on osteoblasts or its inhibition of synthesis of sex hormone-binding globulin. However, the present data do not establish that insulin underlies the fat mass-bone density relationship at all skeletal sites.
引用
收藏
页码:E655 / E659
页数:5
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