In animal models, prostaglandin synthesis has been found to mediate bone me
tabolism. Nonsteroidal anti-inflammatory drugs (NSAIDs), given their inhibi
tory effects of prostaglandin synthesis, may play a role in the prevention
of osteoporosis. The primary objective of this study is to describe and qua
ntify the fracture risks of patients exposed to NSAIDs in a representative
general medical practice setting. A retrospective cohort study was conducte
d in a general medical practice setting in the UK (using data from the Gene
ral Practice Research Database). Regular NSAID users (who received three or
more NSAID prescriptions), aged 18 years or older, were compared with matc
hed control patients and incidental NSAID users. The study comprised 214,57
7 regular NSAID users, 286,850 incidental NSAID users, and 214,577 control
patients. The relative rate of nonvertebral fractures during regular NSAID
treatment compared with control was 1.47 (95% confidence interval [CI] 1.42
-1.52) and that of hip fracture 1.08 (0.98-1.19); No differences in nonvert
ebral fractures were found between the regular and incidental NSAID users (
RR = 1.04; 95% CI 0.99-1.09), The rate of nonvertebral fractures among user
s of diclofenac (RR = 1.00; 95% CI 0.93-1.08) and naproxen (RR = 0.91; 95%
CI 0.82-1.00) was similar to that of ibuprofen, The results of this study a
re not supportive of clinically significant effects of NSAIDs on bone metab
olism. (Bone 27:563-568; 2000) (C) 2000 by Elsevier Science Inc. All rights
reserved.