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Relationships between serum adiponectin, leptin concentrations and bone mineral density, and bone biochemical markers in Chinese women

Authors :
Wu, Nan
Wang, Qing-Ping
Li, Hui
Wu, Xian-Ping
Sun, Zhen-Qiu
Luo, Xiang-Hang
Source :
Clinica Chimica Acta. May2010, Vol. 411 Issue 9/10, p771-775. 5p.
Publication Year :
2010

Abstract

Abstract: Background: Adiponectin and leptin, as the main circulating peptides secreted by adipose tissue, are potential contributors to bone metabolism. However, their association with bone mineral density (BMD) is unknown. We investigated whether these serum adipocytokines concentrations are associated with BMD and bone turnover markers. Methods: Serum adiponectin, leptin concentrations, bone turnover biochemical markers, and BMD were determined in 265 premenopausal and 336 postmenopausal Chinese women. Results: In postmenopausal Chinese women, the multiple linear stepwise regression analysis showed that year since menopause, lean mass, estradiol, and adiponectin, but not fat mass, leptin, were independent predictors of BMD in postmenopausal Chinese women. However, in premenopausal Chinese women, adiponectin was not the predictor of BMD. The significant positive correlations between adiponectin and bone-specific alkaline phosphatase (BAP), bone cross-linked N-telopeptides of type I collagen (NTX) were found only in postmenopausal women. Serum BAP, and NTX, but not adiponectin, decreased in response to alendronate therapy. Conclusions: Adiponectin was an independent predictor of BMD, and positively correlated with bone turnover biochemical markers in postmenopausal Chinese women, but not premenopausal women. It suggested that adiponectin may exert a negative effect on bone mass by promoting excessive bone resorption associated with bone loss. However, these effects may be mediated by menopausal status. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00098981
Volume :
411
Issue :
9/10
Database :
Academic Search Index
Journal :
Clinica Chimica Acta
Publication Type :
Academic Journal
Accession number :
48893473
Full Text :
https://doi.org/10.1016/j.cca.2010.02.064