Early Protection Against Sudden Death by n-3 Polyunsaturated Fatty Acids After Myocardial Infarction

Roberto Marchioli(Mario Negri Sud Foundation), Federica Barzi(Mario Negri Sud Foundation), Elena Bomba(Mario Negri Sud Foundation), Carmine Chieffo(Mario Negri Sud Foundation), Domenico Di Gregorio(Mario Negri Sud Foundation), Rocco Di Mascio(Mario Negri Sud Foundation), Maria Grazia Franzosi(Mario Negri Sud Foundation), Enrico Geraci(Mario Negri Sud Foundation), Giacomo Levantesi(Mario Negri Sud Foundation), Aldo P. Maggioni(Mario Negri Sud Foundation), L Mantini(Mario Negri Sud Foundation), Rosa Maria Marfisi(Mario Negri Sud Foundation), G. Mastrogiuseppe(Mario Negri Sud Foundation), N Mininni(Mario Negri Sud Foundation), Gian Luigi Nicolosi(Mario Negri Sud Foundation), Massimo Santini(Mario Negri Sud Foundation), Carlo Schweiger(Mario Negri Sud Foundation), Luigi Tavazzi(Mario Negri Sud Foundation), Gianni Tognoni(Mario Negri Sud Foundation), C Tucci(Mario Negri Sud Foundation), Franco Valagussa(Mario Negri Sud Foundation)
Circulation
April 23, 2002
Cited by 1,305Open Access
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Abstract

BACKGROUND: Our purpose was to assess the time course of the benefit of n-3 polyunsaturated fatty acids (PUFAs) on mortality documented by the GISSI-Prevenzione trial in patients surviving a recent (<3 months) myocardial infarction. METHODS AND RESULTS: In this study, 11 323 patients were randomly assigned to supplements of n-3 PUFAs, vitamin E (300 mg/d), both, or no treatment (control) on top of optimal pharmacological treatment and lifestyle advice. Intention-to-treat analysis adjusted for interaction between treatments was carried out. Early efficacy of n-3 PUFA treatment for total, cardiovascular, cardiac, coronary, and sudden death; nonfatal myocardial infarction; total coronary heart disease; and cerebrovascular events was assessed by right-censoring follow-up data 12 times from the first month after randomization up to 12 months. Survival curves for n-3 PUFA treatment diverged early after randomization, and total mortality was significantly lowered after 3 months of treatment (relative risk [RR] 0.59; 95% CI 0.36 to 0.97; P=0.037). The reduction in risk of sudden death was specifically relevant and statistically significant already at 4 months (RR 0.47; 95% CI 0.219 to 0.995; P=0.048). A similarly significant, although delayed, pattern after 6 to 8 months of treatment was observed for cardiovascular, cardiac, and coronary deaths. CONCLUSIONS: The early effect of low-dose (1 g/d) n-3 PUFAs on total mortality and sudden death supports the hypothesis of an antiarrhythmic effect of this drug. Such a result is consistent with the wealth of evidence coming from laboratory experiments on isolated myocytes, animal models, and epidemiological and clinical studies.


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