In European population-based studies find more prevalence figures in the order of 13%, 20%, and 30% are found in age groups 50–59, 60–69, and 70–79, respectively [28, 29]. Our corresponding figures of 22%, 28%, and 49% are significantly higher, probably as a result of the characteristics of our population. Prevalence in Europe appears to be relatively high compared to other places in the world [28, 29]. Our results seem to confirm again that the vertebral fractures status is Daporinad mouse largely independent of the bone density. This is illustrated by our finding that even in patients with normal bone density a vertebral fracture was found in 14% (Table 4). This percentage rose to 21% in patients with osteopenia
and to 33% in patients with osteoporosis. Our findings and interpretations are also in agreement with the conclusions of the comprehensive review on VFA by Lewiecki et al. [11]. This study was performed in an “academic” Dutch population, where many patients were assessed for secondary osteoporosis with a wide variety of medical conditions. It is not a population-based study.
However, in this cohort we found a lower rate of vertebral fractures among patients studied because of secondary osteoporosis Cell Cycle inhibitor as compared to primary osteoporosis. The latter group contained however many patients referred from the fracture clinics. Although not the primary aim of this study, the results Sinomenine also confirm the well-known variables associated with higher vertebral fracture risk, such as age, BMD, postmenopausal status in women, history of fractures, use of steroids, self-reported posture change (Table 2, 3). In 2008 the International Society of Clinical Densitometry published a position statement on the application of VFA [12]. Appropriate indications were very complex, and include postmenopausal women with osteopenia and additionally combinations of age group, historical height loss >4 cm, prospective height loss of >2 cm, self-reported prior vertebral fracture, chronic systemic
disease associated with increased risk of vertebral fracture. For men similar complex indications are described including only men with osteopenia and combinations of age group, height loss levels, self-reported vertebral fracture, androgen deprivation therapy and chronic diseases. In addition, all women on glucocorticoid therapy and all persons with osteoporosis by BMD criteria in whom vertebral fractures would alter management were considered indications for VFA. The general purpose of all these variables is to select a subgroup with a higher a priori likelihood of finding a vertebral fracture to improve cost-effectiveness. However, the cost of VFA is low and the prevalence of vertebral fractures is already >10% in patients over 30 years of age and rises rapidly with advancing age (Table 3). This suggests that there is no real need to select subgroups to raise the diagnostic yield.