The relationship of health-related quality of life to prevalent and incident vertebral fractures in postmenopausal women with osteoporosis - Results from the multiple outcomes of raloxifene evaluation study
Sl. Silverman et al., The relationship of health-related quality of life to prevalent and incident vertebral fractures in postmenopausal women with osteoporosis - Results from the multiple outcomes of raloxifene evaluation study, ARTH RHEUM, 44(11), 2001, pp. 2611-2619
Objective. To examine the effect of both Prevalent and incident vertebral f
ractures on health-related quality of life (HRQOL) in postmenopausal women
with osteoporosis and to characterize the effect of prevalent vertebral fra
ctures on HRQOL with respect to number, location, severity, and adjacency.
Methods. Participants were a subset of women (n = 1,395, mean age 68.5 year
s) from the Multiple Outcomes of Raloxifene Evaluation trial who had low bo
ne mineral density and/or prevalent vertebral fractures. Vertebral fracture
s were measured by radiography at baseline, 2 years, and 3 years. HRQOL was
assessed using the Osteoporosis Assessment Questionnaire (OPAQ), a validat
ed disease-targeted instrument, at baseline and annually for 3 years.
Results. Both prevalent and incident radiographic vertebral fractures were
associated with decreased HRQOL. At baseline, women with a prevalent verteb
ral fracture had significantly lower OPAQ scores on physical function, emot
ional status, clinical symptoms, and overall HRQOL compared with women with
out a prevalent fracture (all P < 0.01). HRQOL scores were lower with each
subsequent fracture. The effect of prevalent vertebral fracture was depende
nt on the location within the spine and was strongest in the lumbar region
(L1-L4). Incident vertebral fractures significantly decreased OPAQ scores o
n physical function, emotional status, clinical symptoms, and overall HRQOL
(all P < 0.001).
Conclusion. Our findings demonstrate the importance of treating postmenopau
sal women who have prevalent vertebral fractures to prevent further decreas
es in HRQOL associated with subsequent incident vertebral fracture.