Identification and fracture outcomes of undiagnosed low bone mineral density in postmenopausal women - Results from the National Osteoporosis Risk Assessment
Es. Siris et al., Identification and fracture outcomes of undiagnosed low bone mineral density in postmenopausal women - Results from the National Osteoporosis Risk Assessment, J AM MED A, 286(22), 2001, pp. 2815-2822
Citations number
43
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Context Large segments of the population at risk for osteoporosis and fract
ure have not been evaluated, and the usefulness of peripheral measurements
for short-term prediction of fracture risk is uncertain.
Objectives To describe the occurrence of low bone mineral density (BMD) in
postmenopausal women, its risk factors, and fracture incidence during short
-term follow-up.
Design The National Osteoporosis Risk Assessment, a longitudinal observatio
nal study initiated September 1997 to March 1999, with approximately 12 mon
ths of subsequent follow-up.
Setting and Participants A total of 200160 ambulatory postmenopausal women
aged 50 years or older with no previous osteoporosis diagnosis, derived fro
m 4236 primary care practices in 34 states.
Main Outcome Measures Baseline BMD T scores, obtained from peripheral bone
densitometry performed at the heel, finger, or forearm; risk factors for lo
w BMD, derived from questionnaire responses; and clinical fracture rates at
12-month follow-up.
Results Using World Health Organization criteria, 39.6% had osteopenia (T s
core of -1 to -2.49) and 7.2% had osteoporosis (T score less than or equal
to -2.5). Age, personal or family history of fracture, Asian or Hispanic he
ritage, smoking, and cortisone use were associated with significantly incre
ased likelihood of osteoporosis; higher body mass index, African American h
eritage, estrogen or diuretic use, exercise, and alcohol consumption signif
icantly decreased the likelihood. Among the 163 979 participants with follo
w-up information, osteoporosis was associated with a fracture rate approxim
ately 4 times that of normal BMD (rate ratio, 4.03; 95% confidence interval
[CII, 3.59-4.53) and osteopenia was associated with a 1.8-fold higher rate
(95% Cl, 1.49-2.18).
Conclusions Almost half of this population had previously undetected low BM
D, including 7% with osteoporosis. Peripheral BMD results were highly predi
ctive of fracture risk. Given the economic and social costs of osteoporotic
fractures, strategies to identify and manage osteoporosis in the primary c
are setting need to be established and implemented.