Biological Therapies for Cardiac Arrhythmias Can Genes and Cells Replace Drugs and Devices?

被引:78
作者
Cho, Hee Cheol [1 ]
Marban, Eduardo [1 ]
机构
[1] Cedars Sinai Heart Inst, Los Angeles, CA 90048 USA
关键词
bradycardia; tachycardia; gene therapy; cell therapy; MESENCHYMAL STEM-CELLS; IN-VIVO; INTRACELLULAR CALCIUM; ATRIAL-FIBRILLATION; CHANNEL EXPRESSION; MEDICAL PROGRESS; PURKINJE NEURONS; SINOATRIAL NODE; PACEMAKER; HEART;
D O I
10.1161/CIRCRESAHA.109.212936
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiac rhythm disorders reflect failures of impulse generation and/or conduction. With the exception of ablation methods that yield selective endocardial destruction, present therapies are nonspecific and/or palliative. Progress in understanding the underlying biology opens up prospects for new alternatives. This article reviews the present state of the art in gene- and cell-based therapies to correct cardiac rhythm disturbances. We begin with the rationale for such approaches, briefly discuss efforts to address aspects of tachyarrhythmia, and review advances in creating a biological pacemaker to cure bradyarrhythmia. Insights gained bring the field closer to a paradigm shift away from devices and drugs, and toward biologics, in the treatment of rhythm disorders. ( Circ Res. 2010; 106: 674-685.)
引用
收藏
页码:674 / 685
页数:12
相关论文
共 100 条
[21]   EFFICACY AND SAFETY OF QUINIDINE THERAPY FOR MAINTENANCE OF SINUS RHYTHM AFTER CARDIOVERSION - A METAANALYSIS OF RANDOMIZED CONTROL TRIALS [J].
COPLEN, SE ;
ANTMAN, EM ;
BERLIN, JA ;
HEWITT, P ;
CHALMERS, TC .
CIRCULATION, 1990, 82 (04) :1106-1116
[22]   Role of ablation therapy in ventricular arrhythmias [J].
Das, Mithilesh K. ;
Dandamudi, Gopi ;
Steiner, Hillel .
CARDIOLOGY CLINICS, 2008, 26 (03) :459-+
[23]   Serious workings of the funny current [J].
DiFrancesco, D .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2006, 90 (1-3) :13-25
[24]  
Donahue JK, 2000, NAT MED, V6, P1395
[25]   Acceleration of widespread adenoviral gene transfer to intact rabbit hearts by coronary perfusion with low calcium and serotonin [J].
Donahue, JK ;
Kikkawa, K ;
Thomas, AD ;
Marban, E ;
Lawrence, JH .
GENE THERAPY, 1998, 5 (05) :630-634
[26]   MORTALITY AND MORBIDITY IN PATIENTS RECEIVING ENCAINIDE, FLECAINIDE, OR PLACEBO - THE CARDIAC-ARRHYTHMIA SUPPRESSION TRIAL [J].
ECHT, DS ;
LIEBSON, PR ;
MITCHELL, LB ;
PETERS, RW ;
OBIASMANNO, D ;
BARKER, AH ;
ARENSBERG, D ;
BAKER, A ;
FRIEDMAN, L ;
GREENE, HL ;
HUTHER, ML ;
RICHARDSON, DW .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (12) :781-788
[27]   Enhancement of murine cardiac chronotropy by the molecular transfer of the human β2 adrenergic receptor cDNA [J].
Edelberg, JM ;
Aird, WC ;
Rosenberg, RD .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (02) :337-343
[28]   Molecular enhancement of porcine cardiac chronotropy [J].
Edelberg, JM ;
Huang, DT ;
Josephson, ME ;
Rosenberg, RD .
HEART, 2001, 86 (05) :559-562
[29]  
Ennis IL, 2002, J CLIN INVEST, V109, P393, DOI 10.1172/JCI13359
[30]   Medical progress: Atrial fibrillation. [J].
Falk, RH .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (14) :1067-1078