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绝经后中国女性循环中基质金属蛋白酶-2、基质金属蛋白酶-1和组织金属蛋白酶抑制剂-1水平与骨生化标志物及骨密度的关系

Relationship of circulating MMP-2, MMP-1, and TIMP-1 levels with bone biochemical markers and bone mineral density in postmenopausal Chinese women.

作者信息

Luo X-H, Guo L-J, Shan P-F, Xie H, Wu X-P, Zhang H, Cao X-Z, Yuan L-Q, Liao E-Y

机构信息

Institute of Endocrinology & Metabolism, The Second Xiangya Hospital of Central South University, 410011 Changsha, Hunan, Peoples's Republic of China.

出版信息

Osteoporos Int. 2006;17(4):521-6. doi: 10.1007/s00198-005-0017-6. Epub 2005 Dec 20.

Abstract

INTRODUCTION

Osteoblast-derived matrix metalloproteinase (MMP)-2, MMP-1 and tissue inhibitor of metalloproteinase (TIMP)-1 have been shown to play a role in bone metabolism by degrading the bone matrix.

METHODS

The present study was performed to investigate the relationships between serum MMP-2, MMP-1, or TIMP-1 levels and bone mineral density (BMD), as well as bone biochemical markers, in 297 Chinese postmenopausal women aged 42-80 years.

RESULTS

We found a significant negative weak correlation between MMP-2 and BMD at various skeletal regions. After adjustment for age and BMI, the correlation with BMD at the femoral neck and total hip disappeared. Multiple linear stepwise regression analysis showed that MMP-2 was not a determinant factor for BMD. The significant positive correlations between MMP-2 and bone cross-linked N-telopeptides of type I collagen (NTX), alkaline phosphatase (BAP), and osteocalcin (OC) and were found, and remained significant after adjustment for age and BMI. Moreover, serum MMP-2 concentrations were significantly higher in postmenopausal women with osteoporosis than in age-matched normal controls. There were no significant correlations between MMP-1, TIMP-1 and BMD. There were no significant relationships between MMP-1 and BAP, OC, and NTX. The associations between TIMP-1 and BAP and OC were not specific and constant.

CONCLUSIONS

In conclusion, our results suggest that circulating MMP-2 and markers of bone turnover are correlated, and serum MMP-2 levels may rise with increase in bone turnover.

摘要

引言

成骨细胞衍生的基质金属蛋白酶(MMP)-2、MMP-1和金属蛋白酶组织抑制剂(TIMP)-1已被证明通过降解骨基质在骨代谢中发挥作用。

方法

本研究旨在调查297名年龄在42至80岁的中国绝经后女性血清MMP-2、MMP-1或TIMP-1水平与骨密度(BMD)以及骨生化标志物之间的关系。

结果

我们发现MMP-2与不同骨骼部位的骨密度之间存在显著的负向弱相关性。在对年龄和体重指数进行校正后,与股骨颈和全髋部骨密度的相关性消失。多元线性逐步回归分析表明,MMP-2不是骨密度的决定因素。发现MMP-2与I型胶原交联N-端肽(NTX)、碱性磷酸酶(BAP)和骨钙素(OC)之间存在显著的正相关性,在对年龄和体重指数进行校正后仍显著。此外,骨质疏松症绝经后女性的血清MMP-2浓度显著高于年龄匹配的正常对照组。MMP-1、TIMP-1与骨密度之间无显著相关性。MMP-1与BAP、OC和NTX之间无显著关系。TIMP-1与BAP和OC之间的关联不具有特异性和稳定性。

结论

总之,我们的结果表明循环中的MMP-2与骨转换标志物相关,血清MMP-2水平可能随骨转换增加而升高。

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