The response to oestrogen deprivation of the cartilage collagen degradation marker, CTX-II, is unique compared with other markers of collagen turnover

被引:32
作者
Bay-Jensen, Anne-Christine [1 ]
Tabassi, Nadine C. B. [2 ]
Sondergaard, Lene V. [3 ,4 ]
Andersen, Thomas L. [1 ]
Dagnaes-Hansen, Frederik [4 ]
Garnero, Patrick [2 ]
Kassem, Moustapha [5 ]
Delaisse, Jean-Marie [1 ]
机构
[1] Univ So Denmark, Vejle Hosp, IRS CSFU, Dept Clin Cell Biol, DK-7100 Vejle, Denmark
[2] Synarc, Dept Biomarkers, F-69416 Lyon, France
[3] Aarhus Univ, Inst Human Genet, DK-8000 Aarhus C, Denmark
[4] Aarhus Univ, Dept Microbiol & Immunol, DK-8000 Aarhus C, Denmark
[5] Univ Southern, Dept Clin Endocrinol & Mol Biol, DK-5000 Odense C, Denmark
关键词
ARTICULAR-CARTILAGE; KNEE OSTEOARTHRITIS; POSTMENOPAUSAL WOMEN; REPLACEMENT THERAPY; OVARIECTOMIZED RATS; BIOCHEMICAL MARKERS; JOINT DAMAGE; BONE; EXPRESSION; MENOPAUSE;
D O I
10.1186/ar2596
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Introduction The urinary level of the type II collagen degradation marker CTX-II is increased in postmenopausal women and in ovariectomised rats, suggesting that oestrogen deprivation induces cartilage breakdown. Here we investigate whether this response to oestrogen is also true for other type II collagen turnover markers known to be affected in osteoarthritis, and whether it relates to its presence in specific areas of cartilage tissue. Methods The type II collagen degradation markers CTX-II and HelixII were measured in the body fluids of premenopausal and postmenopausal women and in those of ovariectomised rats receiving oestrogen or not. Levels of PIIANP, a marker of type II collagen synthesis, were also measured in rats. Rat knee cartilage was analysed for immunoreactivity of CTXII and PIIANP and for type II collagen expression. Results As expected, urinary levels of CTX-II are significantly increased in postmenopausal women and also in oestrogen-deprived rats, although only transiently. However, in neither case were these elevations paralleled by a significant increase of Helix-II levels and PIIANP levels did not change at any time. CTX-II immunoreactivity and collagen expression were detected in different cartilage areas. The upper zone is the area where CTX-II immunoreactivity and collagen expression best reflected the differences in urinary levels of CTX-II measured in response to oestrogen. However, correlations between urinary levels of CTX-II and tissue immunostainings in individual rats were not statistically significant. Conclusions We found only a small effect of oestrogen deprivation on cartilage. It was detected by CTX-II, but not by other type II collagen turnover markers typically affected in osteoarthritis.
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页数:12
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