Risk factors predicting the 'time to first fracture' and its association with imminent fractures: a substudy of the FRISBEE cohort

被引:0
|
作者
de Filette, Jeroen M. K. [1 ]
Charles, Alexia [2 ]
Bellanger, Amelie [2 ]
Iconaru, Laura [1 ]
Baleanu, Felicia [1 ]
Surquin, Murielle [3 ]
Body, Jean-Jacques [1 ,2 ,3 ]
Bergmann, Pierre [2 ,4 ]
机构
[1] Univ Libre Bruxelles, CHU Brugmann, Dept Endocrinol, Pl A Van Gehuchten 4, B-1020 Brussels, Belgium
[2] Univ Libre Bruxelles, CHU Brugmann, Lab Rech Translat, Brussels, Belgium
[3] Univ Libre Bruxelles, CHU Brugmann, Dept Internal Med, Brussels, Belgium
[4] Univ Libre Bruxelles, CHU Brugmann, Dept Nucl Med, Brussels, Belgium
关键词
Osteoporosis; Imminent fracture; FRAX; Garvan; FRISBEE; POSTMENOPAUSAL WOMEN; OSTEOPOROSIS; MANAGEMENT; GUIDELINES; HIP;
D O I
10.1007/s11657-023-01296-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Only previous glucocorticoid use and rheumatoid arthritis were predictors of an early fracture (< 2 years after inclusion). A shorter 'time to first fracture' was not an independent clinical risk factor for imminent fractures. Purpose Risk factors for fragility fractures independent of BMD were assessed in several prediction models. However, predictors of a shorter 'time to first fracture' and its impact on imminent fractures are unknown. Methods We studied the concept of 'time to first fracture' in the FRISBEE ("Fracture RIsk Brussels Epidemiological Enquiry") cohort (3560 postmenopausal women). Validated fractures were divided into 3 groups: first fracture < 2 years, 2-5 years, and > 5 years after inclusion. Factors associated with first fracture risk were evaluated with uni- and multivariate analyses using Cox modeling. We examined 'time to first fracture' as a risk factor for imminent fractures in untreated subjects and in those receiving pharmacological treatment. Results Classical risk factors (age, prior fracture, fall history and low BMD) were associated with first fracture in all groups. Previous glucocorticoids and rheumatoid arthritis (RA) were predictors for fracture < 2 years. Imminent fractures were similar in subjects with or without osteoporosis treatment, despite a higher estimated 10-year risk of fragility fracture in those treated, suggesting that treatment is efficient. 'Time to first fracture' was not an independent risk factor for imminent fractures. Conclusion Among the risk factors considered, previous glucocorticoid use and RA were predictors for early fracture, consistent with the concept of very high risk. The 'time to first validated fracture' was not an independent risk factor for imminent fractures. Patients with a first osteoporotic fracture should thus be considered at very high risk for re-fracture, independent of the 'time to first fracture'.
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页数:7
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