Impact of allopurinol on risk of myocardial infarction

被引:101
作者
Grimaldi-Bensouda, L. [1 ,2 ,3 ]
Alperovitch, A. [4 ,5 ]
Aubrun, E. [1 ]
Danchin, N. [6 ,7 ]
Rossignol, M. [8 ,9 ]
Abenhaim, L. [10 ,11 ]
Richette, P. [12 ,13 ]
机构
[1] LA SER, Paris, France
[2] Conservatoire Natl Arts & Metiers, Paris, France
[3] Inst Pasteur, INSERM, F-75724 Paris, France
[4] Inserm U708 Neuroepidemiol, Bordeaux, France
[5] Univ Bordeaux Segalen, Bordeaux, France
[6] Georges Pompidou European Hosp, AP HP, Coronary Dis Unit, Paris, France
[7] Paris Descartes Univ, Paris, France
[8] Ctr Risk Res, LA SER, Montreal, PQ, Canada
[9] McGill Univ, Dept Epidemiol & Biostat, Montreal, PQ, Canada
[10] London Sch Hyg & Trop Med, Dept Epidemiol, London WC1, England
[11] LA SER Europe Ltd, London, England
[12] Univ Paris 07, Hop Lariboisiere, AP HP, UFR Med,Federat Rhumatol, Paris 10, France
[13] Hop Lariboisiere, Inserm U1132, F-75475 Paris 10, France
关键词
NONSTEROIDAL ANTIINFLAMMATORY DRUGS; LEFT-VENTRICULAR HYPERTROPHY; XANTHINE-OXIDASE INHIBITION; PRACTICE RESEARCH DATABASE; CORONARY-HEART-DISEASE; URIC-ACID; CARDIOVASCULAR RISK; GOUT; HYPERURICEMIA; FEBUXOSTAT;
D O I
10.1136/annrheumdis-2012-202972
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background Gout therapy includes xanthine oxidase inhibitors (XOI) and colchicine, which have both been associated with decreased cardiovascular risk. However, their effects on major cardiac events, such as myocardial infarction (MI), need to be investigated further. Objectives To investigate whether XOIs and colchicine are associated with decreased risk of MI. Methods This case-control study compared patients with first-ever MI and matched controls. Cases were recruited from the Pharmacoepidemiological General Research on MI registry. Controls were selected from a referent population (n= 8444) from general practice settings. Results The study sample consisted of 2277 MI patients and 4849 matched controls. Use of allopurinol was reported by 3.1% of cases and 3.8 of controls, and 1.1% of cases and controls used colchicine. The adjusted OR (95% CI) for MI with allopurinol use was 0.80 (0.59 to 1.09). When using less stringent matching criteria that allowed for inclusion of 2593 cases and 5185 controls, the adjusted OR was 0.73 (0.54 to 0.99). Similar results were found on analysis by sex and hypertension status. Colchicine used was not associated with a decreased risk of MI (aOR= 1.17 (0.70 to 1.93)). Conclusions Allopurinol may be associated with a reduced risk of MI. No decreased risk of MI was found in colchicine users. Besides its urate-lowering property, allopurinol might have a cardioprotective effect.
引用
收藏
页码:836 / 842
页数:7
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