Inhibition of clinical benefits of aspirin on first myocardial infarction by nonsteroidal antiinflammatory drugs

被引:194
作者
Kurth, T
Glynn, RJ
Walker, AM
Chan, KA
Buring, JE
Hennekens, CH
Gaziano, JM
机构
[1] Brigham & Womens Hosp, Dept Med, Div Prevent Med, Boston, MA 02215 USA
[2] Brigham & Womens Hosp, Dept Med, Div Aging, Boston, MA 02215 USA
[3] Brigham & Womens Hosp, Dept Med, Div Cardiovasc Dis, Boston, MA 02215 USA
[4] Harvard Univ, Sch Med, Dept Ambulatory Care & Prevent, Boston, MA USA
[5] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[6] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[7] Boston VA Healthcare Syst, Massachusetts Vet Epidemiol Res & Informat Ctr, Boston, MA USA
[8] Ingenix Pharmaceut Serv, Div Epidemiol, Auburndale, MA USA
[9] Univ Miami, Sch Med, Dept Med, Miami, FL USA
[10] Univ Miami, Sch Med, Dept Epidemiol, Miami, FL USA
[11] Univ Miami, Sch Med, Dept Publ Hlth, Miami, FL USA
[12] Mt Sinai Med Ctr, Miami Heart Inst, Miami Beach, FL 33140 USA
关键词
myocardial infarction; aspirin; prevention; epidemiology;
D O I
10.1161/01.CIR.0000087593.07533.9B
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - There is clear evidence from numerous randomized trials and their meta-analyses that aspirin reduces risks of first myocardial infarction (MI). Recent data also suggest that other nonsteroidal anti-inflammatory drugs ( NSAIDs) may interfere with this benefit of aspirin. Methods and Results - We performed subgroup analysis from a 5-year randomized, double-blind, placebo-controlled trial of 325 mg aspirin on alternate days among 22 071 apparently healthy US male physicians with prospective observational data on use of NSAIDs. A total of 378 MIs were confirmed, 139 in the aspirin group and 239 in the placebo group. Aspirin conferred a statistical extreme ( P < 0.00001) 44% reduction in risk of first MI. Among participants randomized to aspirin, use of NSAIDs on 1 to 59 d/y was not associated with MI ( multivariable adjusted relative risk [RR], 1.21; 95% confidence interval [CI], 0.78 to 1.87), whereas the use of NSAIDs on ≥ 60 d/y was associated with MI ( RR, 2.86; 95% CI, 1.25 to 6.56) compared with no use of NSAIDs. In the placebo group, the RRs for MI across the same categories of NSAID use were 1.14 ( 95% CI, 0.81 to 1.60) and 0.21 ( 95% CI, 0.03 to 1.48). Conclusions - These data suggest that regular but not intermittent use of NSAIDs inhibits the clinical benefits of aspirin. Chance, bias, and confounding remain plausible alternative explanations, despite the prospective design and adjustment for covariates. Nonetheless, we believe the most plausible interpretation of the data to be that regular but not intermittent use of NSAIDs inhibits the clinical benefit of aspirin on first MI.
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页码:1191 / 1195
页数:5
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