Investigating the role of the growth hormone-insulin-like growth factor (GH-IGF) axis as a determinant of male bone mineral density (BMD)

被引:33
作者
Patel, MBR
Arden, NK [1 ]
Masterson, LM
Phillips, DIW
Swaminathan, R
Syddall, HE
Byrne, CD
Wood, PJ
Cooper, C
Holt, RIG
机构
[1] Southampton Gen Hosp, MRC, Environm Epidemiol Unit, Southampton SO16 6YD, Hants, England
[2] Southampton Gen Hosp, Dept Chem Pathol, Southampton SO16 6YD, Hants, England
[3] St Thomas Hosp, Dept Chem Pathol, London SE1 7EH, England
基金
美国国家卫生研究院;
关键词
idiopathic osteoporosis; growth hormone secretion; growth hormone sensitivity; insulin-like growth factor-1;
D O I
10.1016/j.bone.2005.06.016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The GH-IGF axis has profound effects on bone metabolism and may be important in the etiology of idiopathic osteoporosis. Serum IGF-I is often low in men with osteoporosis, which may be attributable to GH hypo-secretion or hepatic GH insensitivity. We studied the GH-IGF axis in depth to look for evidence to support these hypotheses. Materials and methods: 28 healthy 60- to 70-year-old men with low, intermediate, or normal BMD were studied. GH secretion was measured by overnight urine collection. GH reserve was assessed by exercise and glucagon stimulation tests. Hepatic IGF-I production was investigated using a GH-IGF-I generation test. Data were analyzed using Pearson's correlation coefficient, linear regression, and analysis of variance. Results: Serum IGF-I was reduced in Subjects with low BMD (P = 0.009). There was no difference in GH secretion or reserve between the groups. Overall, GH reserve and IGF-I were positively related but this was attenuated in the low BMD group. However, no statistically significant difference in IGF-I generation capacity between BMD groups was found. Conclusions: Men with reduced BNID have low IGF-I but normal GH secretion and reserve. Our data suggested, but could not confirm, hepatic resistance to GH as a mechanism for this association. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:833 / 841
页数:9
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