Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome

被引:211
作者
Lahrouchi, Najim [1 ]
Raju, Hariharan [2 ,3 ]
Lodder, Elisabeth M. [1 ]
Papatheodorou, Efstathios [2 ,3 ]
Ware, James S. [4 ,5 ]
Papadakis, Michael [2 ,3 ]
Tadros, Rafik [1 ,6 ,7 ]
Cole, Della [2 ,3 ]
Skinner, Jonathan R. [8 ,9 ]
Crawford, Jackie [8 ,9 ]
Love, Donald R. [8 ,9 ]
Pua, Chee J. [10 ]
Soh, Bee Y. [10 ]
Bhalshankar, Jaydutt D. [10 ]
Govind, Risha
Tfelt-Hansen, Jacob [11 ]
Winkel, Bo G. [11 ]
van der Werf, Christian
Wijeyeratne, Yanushi D. [2 ,3 ]
Mellor, Greg [2 ,3 ]
Till, Jan [3 ,4 ]
Cohen, Marta C. [12 ]
Tome-Esteban, Maria
Sharma, Sanjay
Wilde, Arthur A. M. [1 ,13 ]
Cook, Stuart A. [4 ,10 ,14 ]
Bezzina, Connie R. [1 ]
Sheppard, Mary N. [2 ,3 ]
Behr, Elijah R. [2 ,3 ]
机构
[1] Acad Med Ctr, Dept Clin & Expt Cardiol, Heart Ctr, Amsterdam, Netherlands
[2] St Georges Univ London, Mol & Clin Sci Res Inst, London, England
[3] St Georges Univ Hosp NHS Fdn Trust, Cardiol Clin Acad Grp, London, England
[4] Imperial Coll London, Natl Heart & Lung Inst, Sydney St, London, England
[5] Royal Brompton & Harefield Hosp NHS Fdn Trust, London, England
[6] Montreal Heart Inst, Dept Med, Cardiovasc Genet Ctr, Montreal, PQ, Canada
[7] Univ Montreal, Montreal, PQ, Canada
[8] Starship Childrens Hosp, Green Lane Paediat & Congenital Cardiac Serv, Cardiac Inherited Dis Grp New Zealand, Auckland, New Zealand
[9] Univ Auckland, Dept Paediat Child & Youth Hlth, Auckland, New Zealand
[10] Natl Heart Ctr Singapore, Singapore, Singapore
[11] Rigshosp, Dept Cardiol, Copenhagen, Denmark
[12] Sheffield Childrens NHS Fdn Trust, Sheffield, S Yorkshire, England
[13] Princess Al Jawhara Al Brahim Ctr Excellence Res, Jeddah, Saudi Arabia
[14] Duke Natl Univ Singapore, Singapore, Singapore
基金
英国惠康基金;
关键词
cardiomyopathy; channelopathy; molecular autopsy; next-generation sequencing; unexplained sudden death; CARDIAC DEATH; MOLECULAR AUTOPSY; YOUNG; ASSOCIATION; VARIANTS; ABNORMALITIES; DISEASE; RISK;
D O I
10.1016/j.jacc.2017.02.046
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Sudden arrhythmic death syndrome (SADS) describes a sudden death with negative autopsy and toxicological analysis. Cardiac genetic disease is a likely etiology. OBJECTIVES This study investigated the clinical utility and combined yield of post-mortem genetic testing (molecular autopsy) in cases of SADS and comprehensive clinical evaluation of surviving relatives. METHODS We evaluated 302 expertly validated SADS cases with suitable DNA (median age: 24 years; 65% males) who underwent next-generation sequencing using an extended panel of 77 primary electrical disorder and cardiomyopathy genes. Pathogenic and likely pathogenic variants were classified using American College of Medical Genetics (ACMG) consensus guidelines. The yield of combined molecular autopsy and clinical evaluation in 82 surviving families was evaluated. A gene-level rare variant association analysis was conducted in SADS cases versus controls. RESULTS A clinically actionable pathogenic or likely pathogenic variant was identified in 40 of 302 cases (13%). The main etiologies established were catecholaminergic polymorphic ventricular tachycardia and long QT syndrome (17 [6%] and 11 [4%], respectively). Gene-based rare variants association analysis showed enrichment of rare predicted deleterious variants in RYR2 (p = 5 x 10(-5)). Combining molecular autopsy with clinical evaluation in surviving families increased diagnostic yield from 26% to 39%. CONCLUSIONS Molecular autopsy for electrical disorder and cardiomyopathy genes, using ACMG guidelines for variant classification, identified a modest but realistic yield in SADS. Our data highlighted the predominant role of catecholaminergic polymorphic ventricular tachycardia and long QT syndrome, especially the RYR2 gene, as well as the minimal yield from other genes. Furthermore, we showed the enhanced utility of combined clinical and genetic evaluation. (C) 2017 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.
引用
收藏
页码:2134 / 2145
页数:12
相关论文
共 32 条
[1]  
Ackerman MJ, 2011, HEART RHYTHM, V8, P1308, DOI [10.1093/europace/eur245, 10.1016/j.hrthm.2011.05.020]
[2]   The Ensembl gene annotation system [J].
Aken, Bronwen L. ;
Ayling, Sarah ;
Barrell, Daniel ;
Clarke, Laura ;
Curwen, Valery ;
Fairley, Susan ;
Banet, Julio Fernandez ;
Billis, Konstantinos ;
Giron, Carlos Garcia ;
Hourlier, Thibaut ;
Howe, Kevin ;
Kahari, Andreas ;
Kokocinski, Felix ;
Martin, Fergal J. ;
Murphy, Daniel N. ;
Nag, Rishi ;
Ruffier, Magali ;
Schuster, Michael ;
Tang, Y. Amy ;
Vogel, Jan-Hinnerk ;
White, Simon ;
Zadissa, Amonida ;
Flicek, Paul ;
Searle, Stephen M. J. .
DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION, 2016,
[3]  
Antzelevitch C, 2016, EUROPACE
[4]   A Prospective Study of Sudden Cardiac Death among Children and Young Adults [J].
Bagnall, R. D. ;
Weintraub, R. G. ;
Ingles, J. ;
Duflou, J. ;
Yeates, L. ;
Lam, L. ;
Davis, A. M. ;
Thompson, T. ;
Connell, V. ;
Wallace, J. ;
Naylor, C. ;
Crawford, J. ;
Love, D. R. ;
Hallam, L. ;
White, J. ;
Lawrence, C. ;
Lynch, M. ;
Morgan, N. ;
James, P. ;
du Sart, D. ;
Puranik, R. ;
Langlois, N. ;
Vohra, J. ;
Winship, I. ;
Atherton, J. ;
McGaughran, J. ;
Skinner, J. R. ;
Semsarian, C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2016, 374 (25) :2441-2452
[5]   Exome analysis-based molecular autopsy in cases of sudden unexplained death in the young [J].
Bagnall, Richard D. ;
Das, Jipin ;
Duflou, Johan ;
Semsarian, Christopher .
HEART RHYTHM, 2014, 11 (04) :655-662
[6]   Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome [J].
Behr, E ;
Wood, DA ;
Wright, M ;
Syrris, P ;
Sheppard, MN ;
Casey, A ;
Davies, MJ ;
McKenna, W .
LANCET, 2003, 362 (9394) :1457-1459
[7]   Sudden arrhythmic death syndrome: a national survey of sudden unexplained cardiac death [J].
Behr, E. R. ;
Casey, A. ;
Sheppard, M. ;
Wright, M. ;
Bowker, T. J. ;
Davies, M. J. ;
McKenna, W. J. ;
Wood, D. A. .
HEART, 2007, 93 (05) :601-605
[8]   Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families [J].
Behr, Elijah R. ;
Dalageorgou, Chrysouta ;
Christiansen, Michael ;
Syrris, Petros ;
Hughes, Sian ;
Esteban, Maria T. Tome ;
Rowland, Edward ;
Jeffery, Steve ;
McKenna, William J. .
EUROPEAN HEART JOURNAL, 2008, 29 (13) :1670-1680
[9]   Genetics of Sudden Cardiac Death [J].
Bezzina, Connie R. ;
Lahrouchi, Najim ;
Priori, Silvia G. .
CIRCULATION RESEARCH, 2015, 116 (12) :1919-1936
[10]   Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death [J].
Bezzina, Connie R. ;
Barc, Julien ;
Mizusawa, Yuka ;
Remme, Carol Ann ;
Gourraud, Jean-Baptiste ;
Simonet, Floriane ;
Verkerk, Arie O. ;
Schwartz, Peter J. ;
Crotti, Lia ;
Dagradi, Federica ;
Guicheney, Pascale ;
Fressart, Veronique ;
Leenhardt, Antoine ;
Antzelevitch, Charles ;
Bartkowiak, Susan ;
Schulze-Bahr, Eric ;
Zumhagen, Sven ;
Behr, Elijah R. ;
Bastiaenen, Rachel ;
Tfelt-Hansen, Jacob ;
Olesen, Morten Salling ;
Kaeaeb, Stefan ;
Beckmann, Britt M. ;
Weeke, Peter ;
Watanabe, Hiroshi ;
Endo, Naoto ;
Minamino, Tohru ;
Horie, Minoru ;
Ohno, Seiko ;
Hasegawa, Kanae ;
Makita, Naomasa ;
Nogami, Akihiko ;
Shimizu, Wataru ;
Aiba, Takeshi ;
Froguel, Philippe ;
Balkau, Beverley ;
Lantieri, Olivier ;
Torchio, Margherita ;
Wiese, Cornelia ;
Weber, David ;
Wolswinkel, Rianne ;
Coronel, Ruben ;
Boukens, Bas J. ;
Bezieau, Stephane ;
Charpentier, Eric ;
Chatel, Stephanie ;
Despres, Aurore ;
Gros, Francoise ;
Kyndt, Florence ;
Lecointe, Simon .
NATURE GENETICS, 2013, 45 (09) :1044-+