TY - JOUR
T1 - Do we need bone mineral density to estimate osteoporotic fracture risk? A 10-year prospective multicentre validation study
AU - Marques, Andreá
AU - Lucas, Raquel
AU - Simões, Eugénia
AU - Verstappen, Suzanne M.M.
AU - Jacobs, Johannes W.G.
AU - Da Silva, Jose A.P.
N1 - Funding Information:
1rheumatology Department, centro Hospitalar e Universitário de coimbra, clínica Universitária de reumatologia, University of coimbra, coimbra, Portugal 2coimbra nursing School, esenfc, Health Sciences research Unit: nursing (UiciSa:e), coimbra, Portugal 3ePiUnit – institute of Public Health and Porto Medical School, University of Porto, Porto, Portugal 4instituto Português de reumatologia, lisboa, Portugal 5arthritis research UK centre for epidemiology, Division of Musculoskeletal & Dermatological Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, the University of Manchester, Manchester, UK 6Department of rheumatology and clinical immunology, University Medical center, Utrecht, the netherlands 7niHr Manchester Biomedical research centre, central Manchester University Hospitals nHS Foundation trust, Manchester academic Health Science centre, Manchester, UK
Publisher Copyright:
© 2017 Article author(s).
PY - 2017/10
Y1 - 2017/10
N2 - Objective Evaluate the performance of FRAX®, with and without bone mineral densitometry (BMD), in predicting the occurrence of fragility fractures over 10 years. Methods Participants aged ≥40 years at baseline, with a complete set of data and a minimum of 8.5 years of follow-up were identified from three cohorts (n=2626). Ten-year fracture risk at baseline were estimated with FRAX® and assessed by comparison with observed fractures and receiver operating characteristic analysis. Results During a mean (SD) follow-up of 9.12 (1.5) years, 178 participants suffered a major osteoporotic (MOP) fracture and 28 sustained a hip fracture. The predictive performance of FRAX® was superior to that of BMD alone for both MOP and hip fractures. The area under the curve (AUC) of FRAX® without BMD was 0.76 (95% CI 0.72 to 0.79) for MOP fractures and 0.78 (95% CI 0.69 to 0.86) for hip fractures. No significant improvements were found when BMD was added to clinical variables to predict either MOP (0.78, 95% CI 0.74 to 0.82, p=0.25) or hip fractures (0.79, 95% CI 0.69 to 0.89, p=0.72). AUCs for FRAX® (with and without BMD) were greater for men than for women. FRAX®, with and without BMD, tended to underestimate the number of MOP fractures and to overestimate the number of hip fractures in females. In men, the number of observed fractures were within the 95% CI of the number predicted, both with and without BMD. Conclusion FRAX® without BMD provided good fracture prediction. Adding BMD to FRAX® did not improve the performance of the tool in the general population.
AB - Objective Evaluate the performance of FRAX®, with and without bone mineral densitometry (BMD), in predicting the occurrence of fragility fractures over 10 years. Methods Participants aged ≥40 years at baseline, with a complete set of data and a minimum of 8.5 years of follow-up were identified from three cohorts (n=2626). Ten-year fracture risk at baseline were estimated with FRAX® and assessed by comparison with observed fractures and receiver operating characteristic analysis. Results During a mean (SD) follow-up of 9.12 (1.5) years, 178 participants suffered a major osteoporotic (MOP) fracture and 28 sustained a hip fracture. The predictive performance of FRAX® was superior to that of BMD alone for both MOP and hip fractures. The area under the curve (AUC) of FRAX® without BMD was 0.76 (95% CI 0.72 to 0.79) for MOP fractures and 0.78 (95% CI 0.69 to 0.86) for hip fractures. No significant improvements were found when BMD was added to clinical variables to predict either MOP (0.78, 95% CI 0.74 to 0.82, p=0.25) or hip fractures (0.79, 95% CI 0.69 to 0.89, p=0.72). AUCs for FRAX® (with and without BMD) were greater for men than for women. FRAX®, with and without BMD, tended to underestimate the number of MOP fractures and to overestimate the number of hip fractures in females. In men, the number of observed fractures were within the 95% CI of the number predicted, both with and without BMD. Conclusion FRAX® without BMD provided good fracture prediction. Adding BMD to FRAX® did not improve the performance of the tool in the general population.
KW - epidemiology
KW - osteoporosis
KW - outcomes research
UR - https://www.scopus.com/pages/publications/85030310542
U2 - 10.1136/rmdopen-2017-000509
DO - 10.1136/rmdopen-2017-000509
M3 - Article
C2 - 29018567
AN - SCOPUS:85030310542
SN - 2056-5933
VL - 3
JO - RMD Open
JF - RMD Open
IS - 2
M1 - e000509
ER -