Low-Dose Naproxen Interferes With the Antiplatelet Effects of Aspirin in Healthy Subjects

被引:45
作者
Anzellotti, Paola [2 ]
Capone, Marta L. [2 ]
Jeyam, Anita [3 ]
Tacconelli, Stefania [2 ]
Bruno, Annalisa [2 ]
Tontodonati, Paola [2 ]
Di Francesco, Luigia [2 ]
Grossi, Linda [2 ]
Renda, Giulia [2 ]
Merciaro, Gabriele
Di Gregorio, Patrizia [2 ,4 ]
Price, Thomas S. [3 ]
Garcia Rodriguez, Luis A. [5 ]
Patrignani, Paola [1 ,2 ]
机构
[1] Univ G DAnnunzio, Dept Med, I-66100 Chieti, Italy
[2] Univ G dAnnunzio, Chieti, Italy
[3] Univ London, London, England
[4] Univ G DAnnunzio, SS Annunziata Hosp, I-66100 Chieti, Italy
[5] Spanish Ctr Pharmacoepidemiol Res, Madrid, Spain
来源
ARTHRITIS AND RHEUMATISM | 2011年 / 63卷 / 03期
关键词
NONSTEROIDAL ANTIINFLAMMATORY DRUGS; CORONARY-HEART-DISEASE; MYOCARDIAL-INFARCTION; CYCLOOXYGENASE INHIBITION; PLATELET CYCLOOXYGENASE; PROSTAGLANDIN SYNTHESIS; CLINICAL-PHARMACOLOGY; GENERAL-POPULATION; RISK; IBUPROFEN;
D O I
10.1002/art.30175
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To investigate whether low-dose naproxen sodium (220 mg twice a day) interferes with aspirin's antiplatelet effect in healthy subjects. Methods. We performed a crossover, open-label study in 9 healthy volunteers. They received for 6 days 3 different treatments separated by 14 days of washout: 1) naproxen 2 hours before aspirin, 2) aspirin 2 hours before naproxen, and 3) aspirin alone. The primary end point was the assessment of serum thromboxane B-2 (TXB2) 24 hours after the administration of naproxen 2 hours before aspirin on day 6 of treatment. In 5 volunteers, the rate of recovery of TXB2 generation (up to 72 hours after drug discontinuation) was assessed in serum and in platelet-rich plasma stimulated with arachidonic acid (AA) or collagen. Results. Twenty-four hours after the last dosing on day 6 in volunteers receiving aspirin alone or aspirin before naproxen, serum TXB2 was almost completely inhibited (median [range] 99.1% [97.4-99.4%] and 99.1% [98.0-99.7%], respectively). Naproxen given before aspirin caused a slightly lower inhibition of serum TXB2 (median [range] 98.0% [90.6-99.4%]) than aspirin alone (P = 0.0007) or aspirin before naproxen (P = 0.0045). All treatments produced a maximal inhibition of AA-induced platelet aggregation. At 24 hours, compared with baseline, collagen-induced platelet aggregation was still inhibited by aspirin alone (P = 0.0003), but not by aspirin given 2 hours before or after naproxen. Compared with administration of aspirin alone, the sequential administration of naproxen and aspirin caused a significant parallel upward shift of the regression lines describing the recovery of platelet TXB2. Conclusion. Sequential administration of 220 mg naproxen twice a day and low-dose aspirin interferes with the irreversible inhibition of platelet cyclooxygenase 1 afforded by aspirin. The interaction was smaller when giving naproxen 2 hours after aspirin. The clinical consequences of these 2 schedules of administration of aspirin with naproxen remain to be studied in randomized clinical trials.
引用
收藏
页码:850 / 859
页数:10
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