Effects of celecoxib and naproxen on renal function in the elderly

被引:193
作者
Whelton, A
Schulman, G
Wallemark, C
Drower, EJ
Isakson, PC
Verburg, KM
Geis, GS
机构
[1] Universal Clin Res Ctr Inc, Baltimore, MD USA
[2] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[3] Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN USA
[4] Searle Res & Dev, Skokie, IL USA
关键词
D O I
10.1001/archinte.160.10.1465
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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, randomized, 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 received naproxen, 500 mg twice daily, for 10 days. After a 7-day washout, subjects were crossed over to receive the other regimen. Results: After the first dose, the trend was for a greater decrease in glomerular 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 became 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 and 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 prostaglandin excretion between these 2 agents (P greater than or equal to.07). Small, transient decreases (P<.05) in urinary sodium excretion were observed after the initiation of both celecoxib and naproxen treatment. Sodium excretion 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.
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页码:1465 / 1470
页数:6
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