Yield of Genetic Screening in Inherited Cardiac Channelopathies How to Prioritize Access to Genetic Testing

被引:97
作者
Bai, Rong [1 ,4 ]
Napolitano, Carlo [1 ]
Bloise, Raffaella [1 ]
Monteforte, Nicola [1 ]
Priori, Silvia G. [1 ,2 ,3 ]
机构
[1] IRCCS Fdn Salvatore Maugeri, Pavia, Italy
[2] Univ Pavia, Salvatore Maugeri Fdn, Dept Cardiol, I-27100 Pavia, Italy
[3] NYU, Leon Charney Div Cardiol, Cardiovasc Genet Program, New York, NY USA
[4] Huazhong Univ Sci & Technol, Tong Ji Med Coll, Tong Ji Hosp, Dept Cardiol Intemal Med, Wuhan 430074, Peoples R China
关键词
genetics; long-QT syndrome; catecholaminergic VT; Brugada syndrome; LONG-QT SYNDROME; BRUGADA-SYNDROME; RISK STRATIFICATION; MUTATIONS;
D O I
10.1161/CIRCEP.108.782888
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Identification of mutations in cardiac ion channel genes concurs to the diagnosis of long-QT syndrome, Brugada syndrome, and catecholaminergic polymorphic ventricular tachycardia. However, because availability of genetic screening is still limited and reimbursement policies are lacking, there is a need of evidence-based criteria to prioritize access to genetic testing for these diseases. Methods and Results-We determined the yield of genetic testing and cost per positive genotyping in 1394 consecutive probands. Among the 546 patients referred for long-QT syndrome-genes screening, those with clinical diagnosis of long-QT syndrome had the highest yield (64%) and lowest cost (US $8418) for each positive genotyping. Among 798 individuals screened for mutation on the SCN5A gene, the highest yield was obtained in patients with type I Brugada syndrome ECG pattern (51 of 405; 13%) corresponding to a cost of US $21 441 per positive genotyping. In conclusive Brugada syndrome patients the presence of atrioventricular block(odds ratio: 3.3, CI: 1.8 to 6.1; P=0.0001) increases the yield (23%) of genotyping and reduces its cost (US $ 11700). Among 175 patients screened on RyR2 gene, those with documented bidirectional ventricular tachycardia had the highest incidence (62%) of mutations and the lowest cost (US $5263) per positive genotyping. Genetic screening of unselected family members of sudden cardiac death victims and idiopathic ventricular fibrillation survivors is largely ineffective (yield of 9%) and costly (US $71430 per I positive genotyping). Conclusions-Genotyping can be performed at reasonable cost in individuals with conclusive diagnosis of long-QT syndrome and catecholaminergic polymorphic ventricular tachycardia, and in patients with type I Brugada syndrome ECG with atrioventricular block. These patients should be given priority to access genetic testing. (Circ Arrhythmia Electrophysiol. 2009;2:6-15.)
引用
收藏
页码:6 / 15
页数:10
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