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离子通道相关基因在心肌梗死后恶性心律失常中的研究进展 被引量:1

Research Progress of the Relationship between Gene and Malignant Arrhythmia Related to Post-my ocardial Infarction
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摘要 恶性心律失常是心肌梗死常见和严重的并发症,是一种复杂的病理过程,至今发病机制尚未完全阐明。近年来SCN5A、KCNQ1、KCNE1、KCNH2等离子通道相关基因的作用越来越受到重视,其参与心肌梗死后恶性心律失常的产生。目前基因治疗已开始应用于动物模型,早期实验及应用前景令人鼓舞。现就基因在心肌梗死后恶性心率失常的研究进展予以综述。 Malignant arrhythmia is a complex pathological process and a common complication following myocardial infarction(MI).The pathogenesis of malignant arrhythmia remains unclear.In recent years,there is an increasingly emphasis on the role of genes.Researches have shown that gene participates in the ocur rence of malignant arrhythmia after MI and gene therapy has been used in animal models.This article reviews the effects of gene on the arrhythmia related to post-MI.
作者 潘炎 王玉璟
出处 《医学综述》 2010年第16期2420-2422,共3页 Medical Recapitulate
关键词 心肌梗死 恶性心律失常 基因 Myocardial infarction Malignant arrhythmia Gene
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  • 1Solomon SD,Zelenkofske S,McMurray JJ,et al.Sudden death in patients with myocardial infarction and left ventricular dysfunction,heart failure,or both[J].N Engl J Med,2005,352(25):2581-2588.
  • 2Koo SH,Teo WS,Ching CK,et al.Mutation Screening in KCNQ1,HERG,KCNE1,KCNE2 and SCNSA genes in a long QT syndrome family[J].Ann Acad Med Singapore,2007,36(6):394-398.
  • 3Priori SG,Aliot E,Blomstrom-Lundqvist C,et al.Task force on sudden cardiac death of the european society of cardiology[J].Eur Heart J,2001,22(16):1374-1450.
  • 4Roth A,Lurie I.Pause-dependent torsade de pointes following acute myocardial infarction:a variant of the acquired long QT syndrome[J].J Am Coll Cardiol,2001,38(4):1168-1174.
  • 5Hu D,Viskin S,Oliva A,et al.Novel mutation in the SCN5A gene associated with arrhythmia storm developing during acute myocardial infarction[J].Heart Rhythm,2007,4(8):1072-1080.
  • 6Olszak-Wa s kiewicz M,Kubik L,Dziuk M,et al.The association between SCN5A,KCNQ1 and KCNE1 gene polymorphisms and complex ventricular arrhythmias in survivors of myocardial infarction[J].Kardiol Pol,2008,66(8):845-853.
  • 7Poelzing S,Forleo C,Samodell M,et al.SCN5A polymorphism restores traffickingof a brugada syndrome mutation on a separate gene[J].Circulation,2006,114(5):368-376.
  • 8Olszak-Wa s kiewicz M,Dziuk M,Kubik L,et al.Novel KCNQ1 mutations in patientsafter myocardial infarction[J].Cardiol J,2008,15(3):252-260.
  • 9Buratti E,Baralle M,Baralle FE.Defective splicing,disease and therapy:searching for master checkpoints in exon definition[J].Nucleic Acids Res,2006,34(12):3494-3510.
  • 10Ehrlich JR,Zicha S,Coutu P,et al.Atrial fibrillation-associated minK38G/S polymorphism modulates delayed rectifier current and membrane localization[J].Cardiovas Res,2005,67(3):520-528.

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