Effects of celecoxib and naproxen on renal function in the elderly

Citation
A. Whelton et al., Effects of celecoxib and naproxen on renal function in the elderly, ARCH IN MED, 160(10), 2000, pp. 1465-1470
Citations number
36
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Journal title
ARCHIVES OF INTERNAL MEDICINE
ISSN journal
00039926 → ACNP
Volume
160
Issue
10
Year of publication
2000
Pages
1465 - 1470
Database
ISI
SICI code
0003-9926(20000522)160:10<1465:EOCANO>2.0.ZU;2-A
Abstract
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.