Marchioli Roberto, Barzi Federica, Bomba Elena, Chieffo Carmine, Di Gregorio Domenico, Di Mascio Rocco, Franzosi Maria Grazia, Geraci Enrico, Levantesi Giacomo, Maggioni Aldo Pietro, Mantini Loredana, Marfisi Rosa Maria, Mastrogiuseppe G, Mininni Nicola, Nicolosi Gian Luigi, Santini Massimo, Schweiger Carlo, Tavazzi Luigi, Tognoni Gianni, Tucci Corrado, Valagussa Franco
Department of Clinical Pharmacology and Epidemiology, Consorzio Mario Negri Sud, Santa Maria Imbaro, Chieti, Italy.
Circulation. 2002 Apr 23;105(16):1897-903. doi: 10.1161/01.cir.0000014682.14181.f2.
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.
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.
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.
我们的目的是评估n-3多不饱和脂肪酸(PUFAs)对近期(<3个月)心肌梗死存活患者死亡率的有益作用的时间进程,这一作用已在GISSI-Prevenzione试验中得到证实。
在本研究中,11323例患者在接受最佳药物治疗和生活方式建议的基础上,被随机分配接受n-3 PUFAs补充剂、维生素E(300 mg/d)、两者联合补充或不接受任何治疗(对照组)。进行了针对治疗间相互作用进行调整的意向性分析。通过对随机分组后第一个月至12个月的随访数据进行12次右删失,评估n-3 PUFA治疗对全因死亡、心血管死亡、心脏死亡、冠状动脉死亡和猝死;非致命性心肌梗死;全冠心病;以及脑血管事件的早期疗效。n-3 PUFA治疗的生存曲线在随机分组后早期就出现分歧,治疗3个月后全因死亡率显著降低(相对风险[RR] 0.59;95%置信区间0.36至0.97;P = 0.037)。猝死风险的降低在4个月时就特别显著且具有统计学意义(RR 0.47;95%置信区间0.219至0.995;P = 0.048)。在治疗6至8个月后,观察到心血管死亡、心脏死亡和冠状动脉死亡出现了类似的显著但延迟的模式。
低剂量(1 g/d)n-3 PUFAs对全因死亡率和猝死的早期作用支持了该药物具有抗心律失常作用的假说。这一结果与来自分离心肌细胞的实验室实验、动物模型以及流行病学和临床研究的大量证据相一致。