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载脂蛋白E基因多态性对地中海人群中普伐他汀在心肌梗死后生存影响的作用:GISSI-Prevenzione研究

Apolipoprotein E polymorphisms influence effect of pravastatin on survival after myocardial infarction in a Mediterranean population: the GISSI-Prevenzione study.

作者信息

Chiodini Benedetta D, Franzosi Maria Grazia, Barlera Simona, Signorini Stefano, Lewis Cathryn M, D'Orazio Andria, Mocarelli Paolo, Nicolis Enrico, Marchioli Roberto, Tognoni Gianni

机构信息

Division of Genetics and Molecular Medicine, King's College London, London, UK.

出版信息

Eur Heart J. 2007 Aug;28(16):1977-83. doi: 10.1093/eurheartj/ehm196. Epub 2007 Jun 13.

Abstract

AIMS

Controversy exists with regard to the influence of APOE polymorphisms on coronary heart disease development and on the efficacy of statin treatment. we investigated the relationship between apoe, mortality and the response to treatment in Mediterranean myocardial infarction (mi) survivors.

METHODS AND RESULTS

We analysed 3304 Italian patients with MI randomized to pravastatin or no treatment in the GISSI-Prevenzione study, with a mean follow-up time of 23.0 +/- 6.7 months (median 24.3 months). Mortality curves were calculated using Kaplan-Meier method, and differences in survival were tested using the log-rank test. There were 109 deaths during follow-up. Patients treated with pravastatin showed a significant decrease in mortality compared with non-treated patients (HR 0.67, 95% confidence interval 0.45-0.97, P = 0.038). Among the 3304 patients, 554 (16.8%) were epsilon4 carriers and 2750 (83.2%) were non-epsilon4 carriers. No significant difference in terms of mortality was observed between the epsilon4 and the non-epsilon4 carriers (3.61% vs. 3.24%, P = 0.67). However, although in non-epsilon4 carriers no significant difference in mortality was observed between patients treated with pravastatin and non-treated (2.81% vs. 3.67%, P = 0.21), among the epsilon4 carriers a significant reduction in mortality was observed in patients treated compared with non-treated (1.85% vs. 5.28%, P = 0.023).

CONCLUSION

We found that epsilon4 allele is a determinant of pravastatin response in terms of survival. Though in the entire population investigated,we found a beneficial effect of pravastatin in terms of survival, only the epsilon4 carriers seemed to have gained a significant benefit from this treatment. We suggest that the effect of statins is of particular interest in this fraction of the population. Genetic markers can help in identifying patients that benefit more from statin treatment.

摘要

目的

关于载脂蛋白E(APOE)基因多态性对冠心病发展及他汀类药物治疗疗效的影响存在争议。我们调查了地中海地区心肌梗死(MI)幸存者中APOE、死亡率及治疗反应之间的关系。

方法与结果

我们在GISSI-Prevenzione研究中分析了3304例意大利MI患者,这些患者被随机分为普伐他汀治疗组或未治疗组,平均随访时间为23.0±6.7个月(中位数24.3个月)。采用Kaplan-Meier方法计算死亡率曲线,并使用对数秩检验来检验生存率的差异。随访期间有109例死亡。与未治疗患者相比,接受普伐他汀治疗的患者死亡率显著降低(风险比0.67,95%置信区间0.45 - 0.97,P = 0.038)。在这3304例患者中,554例(16.8%)为ε4等位基因携带者,2750例(83.2%)为非ε4等位基因携带者。ε4等位基因携带者和非ε4等位基因携带者之间在死亡率方面未观察到显著差异(3.61%对3.24%,P = 0.67)。然而,虽然在非ε4等位基因携带者中,接受普伐他汀治疗的患者和未治疗患者之间在死亡率上未观察到显著差异(2.81%对3.67%,P = 0.21),但在ε4等位基因携带者中,与未治疗患者相比,接受治疗的患者死亡率显著降低(1.85%对5.28%,P = 0.023)。

结论

我们发现,就生存率而言,ε4等位基因是普伐他汀治疗反应的一个决定因素。尽管在整个研究人群中,我们发现普伐他汀在生存率方面有有益作用,但似乎只有ε4等位基因携带者从这种治疗中获得了显著益处。我们认为他汀类药物的作用在这部分人群中尤其值得关注。基因标志物有助于识别能从他汀类药物治疗中获益更多的患者。

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