Majmudar Maulik D, Tompkins Christine, Bachmann Justin M, Blumenthal Roger S, Marine Joseph E
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Cardiol Rev. 2009 Mar-Apr;17(2):60-9. doi: 10.1097/CRD.0b013e3181861be8.
Sudden cardiac death remains a leading cause of mortality in the United States, with an incidence of 300,000 to 400,000 deaths annually. Despite advances in the management of cardiovascular disease, the only effective treatments proven to reduce the risk of sudden cardiac death are beta-adrenergic blockers and implantable cardioverter-defibrillators. Antiarrhythmic medications are effective at treating symptomatic and asymptomatic ventricular arrhythmias, but several are associated with increased mortality. Although effective at lowering mortality, implantable cardioverter-defibrillators pose an economic burden and some morbidity to patients when associated with frequent shock therapies. Thus, there is renewed interest in developing additional pharmacologic alternatives that could reduce the risk of fatal ventricular arrhythmias. A post hoc analysis of 2 large clinical trials suggested an association between the use of lipid-altering therapy and decreased rates of sudden death. Retrospective review of other clinical trials and experimental data using animal models provide further insight into the potential antiarrhythmic properties of lipid-altering therapy. This review examines the current status of basic science and clinical research that explores the antiarrhythmic properties of lipid-altering therapy, with a focus on 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors (statins) and polyunsaturated fatty acids.
心脏性猝死仍是美国主要的死亡原因,每年有30万至40万人发病。尽管心血管疾病的治疗取得了进展,但唯一经证实可降低心脏性猝死风险的有效治疗方法是β受体阻滞剂和植入式心脏复律除颤器。抗心律失常药物可有效治疗有症状和无症状的室性心律失常,但有几种药物会增加死亡率。虽然植入式心脏复律除颤器能有效降低死亡率,但与频繁电击治疗相关时,会给患者带来经济负担和一些发病率。因此,人们对开发更多可降低致命性室性心律失常风险的药物替代方案重新产生了兴趣。对2项大型临床试验的事后分析表明,使用调脂治疗与猝死率降低之间存在关联。对其他临床试验和使用动物模型的实验数据进行回顾性研究,能进一步深入了解调脂治疗的潜在抗心律失常特性。本综述探讨了探索调脂治疗抗心律失常特性的基础科学和临床研究的现状,重点关注3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂(他汀类药物)和多不饱和脂肪酸。