کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1967824 | 1538757 | 2006 | 6 صفحه PDF | دانلود رایگان |

BackgroundOsteoblast-derived matrix metalloproteinse-1 (MMP-1), MMP-2 and tissue inhibitor of metalloproteinase-1 (TIMP-1) play a role in bone metabolism by degrading bone matrix.MethodsWe measured MMP-1, MMMP-2, TIMP-1 and associated results with age and bone metabolism in 591 Chinese women aged 20–80 y.ResultsSerum MMP-1, MMP-2, and TIMP-1 concentrations exhibited positive correlation with age. Serum concentrations of MMP-1 were higher in 40–69 y old women. The concentrations of MMP-2 were significantly increased in the 50–69 y olds. Serum TIMP-1 concentrations were significantly lower in women aged 30–59 y, and then these were followed by an increase at > 60 y olds. We found a significant negative weaker correlation between MMP-2 and BMD. But multiple linear stepwise regression analysis showed that MMP-2 was not a determinant factor for BMD. There were significant positive correlations between MMP-2 and bone alkaline phosphatase (BAP), osteocalcin (OC), and cross-linked N-telopeptides of type I collagen (NTX).ConclusionsThe serum concentrations of MMP-1, MMP-2, and TIMP-1 exhibit age-related changes, and circulating MMP-2 and bone turnover are related.
Journal: Clinica Chimica Acta - Volume 371, Issues 1–2, September 2006, Pages 137–142