Genome-wide association studies of cardiac electrical phenotypes

被引:19
|
作者
Glinge, Charlotte [1 ,2 ]
Lahrouchi, Najim [1 ]
Jabbari, Reza [2 ]
Tfelt-Hansen, Jacob [2 ,3 ]
Bezzina, Connie R. [1 ]
机构
[1] Univ Amsterdam, Amsterdam Univ Med Ctr, Heart Ctr, Amsterdam Cardiovasc Sci,Dept Clin & Expt Cardiol, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[2] Copenhagen Univ Hosp, Rigshosp, Heart Ctr, Dept Cardiol, Inge Lehmanns Vej 7, DK-2100 Copenhagen, Denmark
[3] Univ Copenhagen, Fac Med Sci, Dept Forens Med, Freder Vs Vej, DK-2100 Copenhagen, Denmark
关键词
Arrhythmias; COMMON GENETIC VARIANT; INDUCED QT PROLONGATION; ATRIAL-FIBRILLATION; BRUGADA SYNDROME; RISK PREDICTION; RARE VARIANTS; SUDDEN-DEATH; VENTRICULAR-FIBRILLATION; SCN5A MUTATIONS; QRS DURATION;
D O I
10.1093/cvr/cvaa144
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The genetic basis of cardiac electrical phenotypes has in the last 25 years been the subject of intense investigation. While in the first years, such efforts were dominated by the study of familial arrhythmia syndromes, in recent years, large consortia of investigators have successfully pursued genome-wide association studies (GWAS) for the identification of single-nucleotide polymorphisms that govern inter-individual variability in electrocardiographic parameters in the general population. We here provide a review of GWAS conducted on cardiac electrical phenotypes in the last 14 years and discuss the implications of these discoveries for our understanding of the genetic basis of disease susceptibility and variability in disease severity. Furthermore, we review functional follow-up studies that have been conducted on GWAS loci associated with cardiac electrical phenotypes and highlight the challenges and opportunities offered by such studies.
引用
收藏
页码:1620 / 1634
页数:15
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