1. Bone loss and the risk of non-vertebral fractures in women and men: the Tromsø study.
- Author
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Ahmed, L. A., Emaus, N., Berntsen, G. K., Bjørnerem, Å., Fønnebø, V., Jørgensen, L., Schirmer, H., Størmer, J., and Joakimsen, R. M.
- Subjects
FOREARM abnormalities ,BONE density ,BONES ,SPINAL injuries ,BONE fractures ,OSTEOPOROSIS in women ,DISEASE risk factors ,ANALYSIS of variance ,CHI-squared test ,COMPUTER software ,CONFIDENCE intervals ,LONGITUDINAL method ,OSTEOPOROSIS ,QUESTIONNAIRES ,RESEARCH funding ,T-test (Statistics) ,X-ray densitometry in medicine ,DATA analysis ,RELATIVE medical risk ,POSTMENOPAUSE ,DISEASE complications - Abstract
We assessed the association between the rate of forearm bone loss and non-vertebral fracture. Bone loss at the distal forearm predicted fractures, independently of baseline BMD, but not independently of follow-up BMD in women. The BMD level where an individual ends up is the significant predictor of fracture risk. Bone loss may predict fracture risk independently of baseline BMD. The influence of follow-up BMD on this prediction is unknown. The aim of this study was to assess the association between bone loss and fracture risk in both sexes in a prospective population-based study. We included 1,208 postmenopausal women (50 to 74 years), and 1,336 men (55 to 74 years) from the Tromsø Study, who had repeated distal and ultra-distal forearm BMD measurements. Non-vertebral fractures were registered from 2001 to 2005. A total of 100 women and 46 men sustained fractures during the follow-up time. Independent of baseline BMD, the RR associated with distal site bone loss of 1 SD %/year was 1.23 (1.01-1.50) for low-trauma fractures (excluding hand, foot, skull & high-trauma) and 1.32 (1.07-1.62) for osteoporotic fractures (hip, wrist and shoulder). However, bone loss did not predict fracture after adjusting for follow-up BMD. The BMD level where an individual ends up became the significant predictor of fracture risk and not the rate of bone loss. Follow-up BMD at ultra-distal site was associated with low-trauma fractures in both sexes. While ultra-distal site BMD changes were not associated with fracture risk in both sexes. Bone loss at the distal forearm predicted non-vertebral fractures, independently of baseline BMD, but not independently of follow-up BMD, in women. The BMD level where an individual ends up is the significant predictor of fracture risk and not the rate of bone loss. [ABSTRACT FROM AUTHOR]
- Published
- 2010
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