Literature DB >> 21070882

Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds.

Jonathan R Skinner1, Jackie Crawford, Warren Smith, Andrew Aitken, David Heaven, Cary-Anne Evans, Ian Hayes, Katherine R Neas, Simon Stables, Timothy Koelmeyer, Lloyd Denmark, Jane Vuletic, Fraser Maxwell, Kate White, Tao Yang, Dan M Roden, Trond P Leren, Andrew Shelling, Donald R Love.   

Abstract

BACKGROUND: Retrospective investigation of sudden unexplained death in the young (SUDY) reveals that a high proportion is due to inherited heart disease.
OBJECTIVE: The purpose of this study was to ascertain the diagnostic value of postmortem long QT (LQT) genetic analysis in a prospective study of SUDY victims 1-40 years old.
METHODS: Denaturing high-performance liquid chromatography or direct sequencing of LQT genes 1, 2, 3, 5, and 6 was performed, in a National New Zealand protocol, in SUDY victims aged 1-40 years.
RESULTS: Over 26 months (2006-2008), DNA was stored at autopsy from 52 victims of sudden unexpected death. Further testing revealed a diagnosis in 19 cases (poisoning 4, dilated cardiomyopathy 3, myocarditis 3, other 9). The remaining 33 cases underwent genetic testing (age at death 18 months-40 years, median 25 years). Eighteen (55%) died during sleep or at rest, and 7 (21%) died during light activity. Rare missense variants in LQT genes were found in 5 (15%) cases (confidence interval 3%-27%): T96R in KCNQ1 (11-year-old male), P968L in KCNH2 (32-year-old female), P2006A in SCN5A (34-year-old female), and R67H and R98W in KCNE1 (17- and 38-year-old females, respectively). Evidence of pathogenicity was provided by in vitro evidence (T96R), family phenotype-genotype co-segregation (R98W, P2006A), and/or previous reports (R67H, P968L, P2006A, R98W). Family cardiac investigation was possible in 23 (70%) families and revealed probable cause of death for 5 (15%) other victims (confidence interval 3%-27%).
CONCLUSION: Most community SUDY occurs at rest or during light activity. A diagnostic rate of 15% supports the transition of LQT genetic autopsy, combined with family investigation, into routine medical practice.
Copyright © 2011 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 21070882     DOI: 10.1016/j.hrthm.2010.11.016

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN: 1547-5271            Impact factor:   6.343


  40 in total

1.  Detection of genetic variation in KCNQ1 gene by high-resolution melting analysis in a prospective-based series of postmortem negative sudden death: comparison of results obtained in fresh frozen and formalin-fixed paraffin-embedded tissues.

Authors:  Audrey Farrugia; Christine Keyser; Bertrand Ludes
Journal:  Int J Legal Med       Date:  2012-03-09       Impact factor: 2.686

2.  Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.

Authors:  David J Tester; Argelia Medeiros-Domingo; Melissa L Will; Carla M Haglund; Michael J Ackerman
Journal:  Mayo Clin Proc       Date:  2012-06       Impact factor: 7.616

Review 3.  The molecular autopsy: should the evaluation continue after the funeral?

Authors:  David J Tester; Michael J Ackerman
Journal:  Pediatr Cardiol       Date:  2012-02-04       Impact factor: 1.655

4.  Sudden Unexplained Death - Treating the Family.

Authors:  Greg Mellor; Elijah R Behr
Journal:  Arrhythm Electrophysiol Rev       Date:  2014-11-29

5.  Sudden death due to catecholaminergic polymorphic ventricular tachycardia following negative stress-test outcome: genetics and clinical implications.

Authors:  Cristian D'Ovidio; Aldo Carnevale; Vincenzo M Grassi; Enrica Rosato; Bernat Del Olmo; Monica Coll; Oscar Campuzano; Anna Iglesias; Ramon Brugada; Antonio Oliva
Journal:  Forensic Sci Med Pathol       Date:  2017-04-13       Impact factor: 2.007

6.  Telltale hearts.

Authors:  Jeanne Erdmann
Journal:  Nat Med       Date:  2013-11       Impact factor: 53.440

7.  Visual automated fluorescence electrophoresis provides simultaneous quality, quantity, and molecular weight spectra for genomic DNA from archived neonatal blood spots.

Authors:  Tara L Klassen; Janice Drabek; Torjbörn Tomson; Olafur Sveinsson; Ulrika von Döbeln; Jeffrey L Noebels; Alicia M Goldman
Journal:  J Mol Diagn       Date:  2013-03-19       Impact factor: 5.568

8.  Plakophilin-2 Truncation Variants in Patients Clinically Diagnosed With Catecholaminergic Polymorphic Ventricular Tachycardia and Decedents With Exercise-Associated Autopsy Negative Sudden Unexplained Death in the Young.

Authors:  David J Tester; Jaeger P Ackerman; John R Giudicessi; Nicholas C Ackerman; Marina Cerrone; Mario Delmar; Michael J Ackerman
Journal:  JACC Clin Electrophysiol       Date:  2018-11-01

9.  Next-generation sequencing of 100 candidate genes in young victims of suspected sudden cardiac death with structural abnormalities of the heart.

Authors:  C L Hertz; S L Christiansen; L Ferrero-Miliani; M Dahl; P E Weeke; G L Ottesen; R Frank-Hansen; H Bundgaard; N Morling
Journal:  Int J Legal Med       Date:  2015-09-17       Impact factor: 2.686

10.  Genetic investigation of 100 heart genes in sudden unexplained death victims in a forensic setting.

Authors:  Sofie Lindgren Christiansen; Christin Løth Hertz; Laura Ferrero-Miliani; Morten Dahl; Peter Ejvin Weeke; Gyda Lolk Ottesen; Rune Frank-Hansen; Henning Bundgaard; Niels Morling
Journal:  Eur J Hum Genet       Date:  2016-09-21       Impact factor: 4.246

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