5 or less). Other clinical risk SHP099 in vitro factors also contribute substantially to fracture risk [41, 42]. The recently introduced FRAX fracture risk assessment tool provides a framework for estimating fracture risk in individuals from clinical risk factors, including age, body mass index, previous fracture, parental history of fracture and current

smoking, with or without the use of BMD [43]. A previous study demonstrated that the efficacy of a 3-year treatment with strontium ranelate on the risk of vertebral fractures is independent of baseline BMD and all of the above clinical risk factors [19]. The present analysis indicates that elevated levels of bone turnover markers is another risk factor for vertebral fracture and shows that the 3-year PD0325901 mw efficacy of strontium

ranelate is also independent of the baseline bone turnover level. Three-year treatment with strontium ranelate therefore reduces vertebral fracture risk in post-menopausal women with a wide spectrum of risk factors for these fractures. The main limitation of this study is that the results were based on post hoc analyses using pooled data from two studies with different entry criteria. However, both studies included women from a common run-in study (the FIRST study), and vertebral fracture, https://www.selleckchem.com/products/BIRB-796-(Doramapimod).html BMD and bone turnover data were collected using the same methodology. There were no significant differences in patients’ characteristics at baseline between the strontium ranelate and placebo groups, and the only differences among patients in the tertiles of bone turnover markers

are related to lumbar and femoral neck BMD. Pooling of data was therefore unlikely to have affected the conclusions of the study. On the other hand, pooling of data allowed an adequate sample size and number of fractures to compare treatments after stratification of patients into tertiles and ensured that women with a wide range of disease severity and bone turnover were included in the analysis. In conclusion, strontium ranelate showed significant vertebral anti-fracture efficacy in post-menopausal osteoporotic women in each tertile of markers of pre-treatment bone formation and resorption. Mannose-binding protein-associated serine protease The relative reductions in vertebral fracture risk achieved by strontium ranelate were independent of baseline bone turnover level. These results indicate that strontium ranelate offers clinical benefits to women across a wide range of metabolic states and disease severity. Conflicts of interest Dr. Collette has no conflict of interest; Dr. Bruyère and Dr. Boonen received some consulting fees; Dr. Kaufman, Dr. Lorenc, Pr Felsenberg and Dr. Spector are investigators in SOTI and TROPOS studies; Pr Reginster received consulting fees, lecture fees and research grants from Servier.