Objective: To compare the effects of celecoxib, a cyclooxygenase 2-specific
inhibitor, with the nonspecific cyclooxygenase 1 and 2 inhibitor naproxen
on renal function in 29 healthy elderly subjects in a single-blind, randomi
zed, crossover study,
Methods: Subjects received either celecoxib, 200 mg twice daily, for 5 days
followed by celecoxib, 400 mg twice daily, for the next 5 days, or they re
ceived naproxen, 500 mg twice daily, for 10 days. After a 7-day washout, su
bjects were crossed over to receive the other regimen.
Results: After the first dose, the trend was for a greater decrease in glom
erular filtration rate with naproxen (-5.31 mL/min per 1.73 m(2)) compared
with celecoxib (-0.86 mL/min per 1.73 m(2)). The treatment difference becam
e statistically significant on day 6 (-7.53 vs -1.11 mL/min per 1.73 m2 for
naproxen and celecoxib, respectively; P=.004). Urinary prostaglandin E-2 a
nd 6-keto-prostaglandin F-1 alpha excretion was significantly reduced from
baseline across the treatment interval with both celecoxib and naproxen (P
less than or equal to.04). There were no significant differences in prostag
landin excretion between these 2 agents (P greater than or equal to.07). Sm
all, transient decreases (P<.05) in urinary sodium excretion were observed
after the initiation of both celecoxib and naproxen treatment. Sodium excre
tion values returned to baseline by the end of the study.
Conclusions: The results indicate that cyclooxygenase 2-specific inhibition
in healthy elderly subjects may spare renal hemodynamic function, although
the effects on sodium excretion, as well as urinary prostaglandin E-2 and
6-keto-prostaglandin F-1 alpha excretion, appear to be similar to those of
nonspecific cyclooxygenase inhibitors such as naproxen.