ABSTRACT
BACKGROUND Undertreatment of osteoporosis has been recognized as a common problem in selected patient subgroups. However, primary prevention
has been hampered by limited risk assessment tools that can be applied to large populations.
OBJECTIVES Using clinical risk factors with a new tool from the World Health Organization (FRAX) and recommendations from the National
Osteoporosis Foundation (NOF), we evaluated fracture risk and osteoporosis treatment in a US cohort.
PARTICIPANTS African Americans and Caucasians recruited from 2003–7 across the US as part of a longitudinal study.
MEASURES The number of persons receiving prescription osteoporosis medications was assessed by race, sex, and fracture risk. Multivariable
logistic regression evaluated the association between receipt of osteoporosis medications and fracture risk after controlling
for potential confounders.
RESULTS Among 24,783 participants, estimated fracture risk was highest for Caucasian women. After multivariable adjustment for fracture-related
risk factors, the likelihood of receipt of osteoporosis medications among African Americans was lower than among Caucasians
[odds ratio (OR) = 0.44, 95% confidence interval (CI) 0.37, 0.53] and for men compared to women (OR = 0.08, 95% CI 0.06–0.10).
Even for the highest risk group, Caucasian women with 10-year hip fracture risk ≥3% (n = 3,025, 39.7%), only 26% were receiving
treatment.
CONCLUSIONS A substantial gap exists between 2008 NOF treatment guidelines based on fracture risk and the receipt of prescription osteoporosis
medications. This gap was particularly notable for African Americans and men. FRAX is likely to be useful to assess risk at
a population level and identify high-risk persons in need of additional evaluation.
- Content Type Journal Article
- Category Original Article
- DOI 10.1007/s11606-009-1031-8
- Authors
- Jeffrey R. Curtis, University of Alabama at Birmingham Division of Clinical Immunology and Rheumatology Birmingham USA
- Leslie A. McClure, University of Alabama at Birmingham Department of Biostatistics Birmingham USA
- Elizabeth Delzell, University of Alabama at Birmingham Department of Epidemiology Birmingham USA
- Virginia J. Howard, University of Alabama at Birmingham Department of Epidemiology Birmingham USA
- Eric Orwoll, Oregon Health Sciences University Department of Medicine Portland OR USA
- Kenneth G. Saag, University of Alabama at Birmingham Division of Clinical Immunology and Rheumatology Birmingham USA
- Monika Safford, University of Alabama at Birmingham Division of Preventive Medicine Birmingham USA
- George Howard, University of Alabama at Birmingham Department of Biostatistics Birmingham USA
Wednesday, June 24, 2009 2:08:26 AM