A1 Refereed original research article in a scientific journal

Prediction of bone loss using biochemical markers of bone turnover




AuthorsLenora J, Ivaska KK, Obrant KJ, Gerdhem P

PublisherSPRINGER LONDON LTD

Publication year2007

JournalOsteoporosis International

Journal name in sourceOSTEOPOROSIS INTERNATIONAL

Journal acronymOSTEOPOROSIS INT

Volume18

Issue9

First page 1297

Last page1305

Number of pages9

ISSN0937-941X

DOIhttps://doi.org/10.1007/s00198-007-0379-z


Abstract
The association between baseline levels of eleven bone turnover markers and 5-year rate of bone density change was prospectively studied in a population-based sample of 601 75-year-old women. Several bone formation and resorption markers as well as urinary osteocalcin were modestly correlated to rate of bone density change.Introduction Prediction of bone loss by bone turnover markers (BTMs) has been investigated with conflicting results. There is limited information in the elderly.Methods Eleven bone turnover markers were analyzed in 75year old women in the OPRA study (n= 601) and compared to the 5-year change of areal bone mineral density (aBMD) in seven skeletal regions.Results Annual aBMD change varied between +0.4% ( spine) and -2.0% ( femoral neck). Significant associations (p < 0.01) were found for four different serum osteocalcins (S-OCs) ( standardized regression coefficient -0.20 to -0.22), urinary deoxypyridinoline (-0.19), serum TRACP5b (-0.19), serum CTX- I (-0.21), two of the three urinary osteocalcins (U-OCs) (-0.16) and aBMD change of the leg region ( derived from the total body measurement). After adjustment for baseline aBMD, associations were found for all S-OCs (-0.11 to -0.16), two of the three U-OCs (-0.14 to -0.16) and aBMD change at the total hip, and for three of the four S-OCs (-0.14 to -0.15), S-TRACP5b (-0.11), two of the three U-OCs (-0.14 to -0.15) and aBMD change at the femoral neck. There were no significant results concerning aBMD change at the spine.Conclusion This study indicates that BTMs are correlated with aBMD loss in some skeletal regions in elderly women.



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