CORRELATIONS BETWEEN THE MARKERS OF BONE REMODELING AND BONE MINERAL DENSITY IN POSTMENOPAUSAL OSTEOPOROSIS

被引:3
作者
Gurban, C. [1 ]
Zosin, I. [2 ]
Gotia, S. [3 ]
Sfrijan, F. [1 ]
Gotia, L. [3 ]
Radulov, I. [5 ]
Savescu, I. [5 ]
Drugarin, D. [4 ]
机构
[1] Victor Babes Univ Med & Pharm, Dept Biochem, Timisoara 300041, Romania
[2] Victor Babes Univ Med & Pharm, Dept Endocrinol, Timisoara 300041, Romania
[3] Victor Babes Univ Med & Pharm, Dept Physiol, Timisoara 300041, Romania
[4] Banat Univ Agr Sci & Vet Med, Dept Chem, Timisoara, Romania
[5] Victor Babes Univ Med & Pharm, Dept Immunol, Timisoara, Romania
关键词
postmenopausal osteoporosis; osteocalcin; bone alkaline phosphatase; bone mineral density; ALKALINE-PHOSPHATASE; THERAPY; MATRIX; WOMEN; SERUM;
D O I
10.4183/aeb.2010.27
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim. To assess the levels of s BGP and BAP and correlate them with the rate of bone remodelling. Patients and Methods. The study was performed on 74 cases with postmenopausal osteoporosis, divided into two groups, according to the duration of estrogenic deprivation, compared with a control group (n= 20, postmenopausal women without osteoporosis). The serum levels of the discussed markers were measured by ELISA technique. BMD was measured using the DXA technique with the assessment of T score. Results. In the group T.: BGP were 20.12 +/- 0.87ng/mL (p<0.03), those of BAP 13.76 +/- 0.6 mu g/mL (p<0.001) and sT spine were -3.63 +/- 0.65DS (p<0.001). In the group II: BGP were 15.12 +/- 1.55ng/mL (p<0.05), those of BAP 11.88 +/- 0.38 mu g/mL (p<0.001) and sT spine were -3.78 +/- 0.36DS (p<0.001). The control group presented: BGP of 16.22 +/- 1.62ng/mL, those of BAP of 8.68 +/- 0.44 mu g/mL and sT spine of -1.78 +/- 0.11DS. The serum levels of BGP in postmenopausal osteoporosis cases were increased in group I (suggesting an osteoblastic activation) and decreased in group II (probably secondary to the stimulation of osteoblastic apoptosis). The serum levels of BAP are significantly increased in postmenopausal osteoporosis versus control group, attesting osteoblastic activation. Conclusion. Bone resorption begins gradually to outrun a new bone formation rhythm associated with low BMD.
引用
收藏
页码:27 / 34
页数:8
相关论文
共 18 条
[1]  
Bhattacharyya S, 2008, J BONE MINER RES, V23, P1106, DOI [10.1359/jbmr.080235, 10.1359/JBMR.080235]
[2]  
BULLON P, 2007, MED ORAL PATOL ORAL, V12, P2
[3]   Transient versus sustained phosphorylation and nuclear accumulation of ERKs underlie anti-versus pro-apoptotic effects of estrogens [J].
Chen, JR ;
Plotkin, LI ;
Aguirre, JI ;
Han, L ;
Jilka, RL ;
Kousteni, S ;
Bellido, T ;
Manolagas, SC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (06) :4632-4638
[4]  
Delmas PD, 2000, OSTEOPOROSIS INT, V11, pS2, DOI 10.1007/s001980070002
[5]  
*DIAGN SYST LAB IN, DSL107600I
[6]   Biomarkers for osteoporosis management - Utility in diagnosis, fracture risk prediction and therapy monitoring [J].
Garnero, Patrick .
MOLECULAR DIAGNOSIS & THERAPY, 2008, 12 (03) :157-170
[7]  
Grigorie D, 2003, Rom J Intern Med, V41, P409
[8]  
*IDS INC, OCTEIAOSTASC BAP EL
[9]   Release of intact and fragmented osteocalcin molecules from bone matrix during bone resorption in vitro [J].
Ivaska, KK ;
Hentunen, TA ;
Vääräniemi, J ;
Ylipahkala, H ;
Pettersson, K ;
Väänänen, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (18) :18361-18369
[10]   Matrix Gla protein inhibition of tooth mineralization [J].
Kaipatur, N. R. ;
Murshed, M. ;
McKee, M. D. .
JOURNAL OF DENTAL RESEARCH, 2008, 87 (09) :839-844