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Submitted on July 6, 2007
Accepted on April 24, 2008
Clinical and Molecular Osteoporosis Research Unit, Lund University, Department of Orthopaedics, Malmö University Hospital, SE-20502 Malmö, Sweden; University of Turku, Institute of Biomedicine, Department of Anatomy, FI-20520 Turku, Finland; Karolinska Institute, Department of Orthopaedics, Karolinska University Hospital, SE-14186 Stockholm, Sweden
* To whom correspondence should be addressed. E-mail: kaisa.ivaska{at}med.lu.se.
Context: One of the important challenges in the management of osteoporosis is to identify women who are at high risk of developing osteoporosis and fragility fractures.
Objective: To evaluate if assessment of bone metabolism at multiple occasions can identify women with the highest risk for bone loss.
Design: The Malmö OPRA study is an ongoing longitudinal study. Participants have been evaluated at baseline and after 1, 3 and 5 years.
Setting: Population-based study.
Participants: 1044 women, all 75 years old at baseline.
Main outcome measures: Seven bone turnover markers were assessed at baseline, 1, 3 and 5 years (n=573). Five year change in areal bone mineral density (aBMD) was also determined.
Results: Baseline markers correlated weakly to change in total body aBMD. The associations were more pronounced when the average of the baseline and 1-year measurements was used (standardized regression coefficients -0.12 to -0.23, p<0.01). Adding the 3-year and 5-year measurement further strengthened the correlation (regression coefficients up to -0.30 (p<0.001)). Women with constantly high turnover lost significantly more bone at total body (-2.6%) than women with intermediate (-1.6%) or low turnover (-0.2%, p for trend <0.001). They also had a greater decrease in hip BMD (-8.3%, -6.0% and -5.1%, respectively, p=0.010). Results were similar also in the subgroup of women with osteopenia.
Conclusions: Our results suggest that serial assessment of bone turnover improves the identification of women with the highest rate of bone loss and osteoporosis risk.
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