Literature DB >> 23631430

Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory.

Krystien V Lieve1, Leah Williams, Amy Daly, Gabriele Richard, Sherri Bale, Daniela Macaya, Wendy K Chung.   

Abstract

AIM: Our aim was to examine the diagnostic yield of genetic testing in 855 consecutive unrelated cases referred for Long QT syndrome (LQTS).
RESULTS: Eight hundred fifty five consecutive patients with a mean age at testing of 27.5±18.6 years, were referred for LQTS genetic testing and had accompanying clinical information. KCNQ1, KCNH2, SCN5A, ANK2, KCNE1, KCNE2, CACNA1C, KCNJ2, CAV3, and SCN4B were analyzed using Next-Generation sequencing in all patients, and 395 patients were also tested for an additional two genes, AKAP9 and SNTA1. We retrospectively analyzed the diagnostic yield of this genetic test and factors that predicted the likelihood of a disease causing mutation using ANOVA, χ2, t-test, and receiver operator curves. At least one mutation was identified in 30.3% of the patients (n=259), and 18 patients (2.1%) had two mutations. Patients with two mutations had a longer QTc interval (p<0.01) than patients with one mutation. A longer QTc duration and family history of LQTS were each associated with a higher yield of positive results on genetic testing (p<0.01 for each). Using a QTc cutoff of 476 msec or greater, the genetic testing had a sensitivity of 72% and a specificity of 49%. Mutations within the transmembrane domain of KCNQ1 were associated with a greater risk of cardiac arrest and syncope relative to mutations in other domains of the gene. Mutations in SCN5A were associated with a higher frequency of cardiac arrest (52.6%).
CONCLUSION: Sequencing-based genetic testing has a sensitivity of 72% and has clinical utility.

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Year:  2013        PMID: 23631430     DOI: 10.1089/gtmb.2012.0118

Source DB:  PubMed          Journal:  Genet Test Mol Biomarkers        ISSN: 1945-0257


  17 in total

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Authors:  Gilles Millat; Valérie Chanavat; Robert Rousson
Journal:  Mol Diagn Ther       Date:  2014-10       Impact factor: 4.074

2.  Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward Syndrome.

Authors:  Rabia Faridi; Risa Tona; Alessandra Brofferio; Michael Hoa; Rafal Olszewski; Isabelle Schrauwen; Muhammad Z K Assir; Akhtar A Bandesha; Asma A Khan; Atteeq U Rehman; Carmen Brewer; Wasim Ahmed; Suzanne M Leal; Sheikh Riazuddin; Steven E Boyden; Thomas B Friedman
Journal:  Hum Mutat       Date:  2018-12-12       Impact factor: 4.878

3.  Reclassification of Variants of Uncertain Significance in Children with Inherited Arrhythmia Syndromes is Predicted by Clinical Factors.

Authors:  Jeffrey S Bennett; Madison Bernhardt; Kim L McBride; Shalini C Reshmi; Erik Zmuda; Naomi J Kertesz; Vidu Garg; Sara Fitzgerald-Butt; Anna N Kamp
Journal:  Pediatr Cardiol       Date:  2019-09-18       Impact factor: 1.655

4.  Genetic variants for long QT syndrome among infants and children from a statewide newborn hearing screening program cohort.

Authors:  Ruey-Kang R Chang; Yueh-Tze Lan; Michael J Silka; Hallie Morrow; Alan Kwong; Janna Smith-Lang; Robert Wallerstein; Henry J Lin
Journal:  J Pediatr       Date:  2013-12-31       Impact factor: 4.406

5.  Amino acid-level signal-to-noise analysis of incidentally identified variants in genes associated with long QT syndrome during pediatric whole exome sequencing reflects background genetic noise.

Authors:  Andrew P Landstrom; Ernesto Fernandez; Jill A Rosenfeld; Yaping Yang; Andrew L Dailey-Schwartz; Christina Y Miyake; Hugh D Allen; Daniel J Penny; Jeffrey J Kim
Journal:  Heart Rhythm       Date:  2018-03-02       Impact factor: 6.343

6.  Early somatic mosaicism is a rare cause of long-QT syndrome.

Authors:  James Rush Priest; Charles Gawad; Kristopher M Kahlig; Joseph K Yu; Thomas O'Hara; Patrick M Boyle; Sridharan Rajamani; Michael J Clark; Sarah T K Garcia; Scott Ceresnak; Jason Harris; Sean Boyle; Frederick E Dewey; Lindsey Malloy-Walton; Kyla Dunn; Megan Grove; Marco V Perez; Norma F Neff; Richard Chen; Katsuhide Maeda; Anne Dubin; Luiz Belardinelli; John West; Christian Antolik; Daniela Macaya; Thomas Quertermous; Natalia A Trayanova; Stephen R Quake; Euan A Ashley
Journal:  Proc Natl Acad Sci U S A       Date:  2016-09-28       Impact factor: 11.205

7.  Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing.

Authors:  James R Priest; Scott R Ceresnak; Frederick E Dewey; Lindsey E Malloy-Walton; Kyla Dunn; Megan E Grove; Marco V Perez; Katsuhide Maeda; Anne M Dubin; Euan A Ashley
Journal:  Heart Rhythm       Date:  2014-06-25       Impact factor: 6.343

8.  Re-evaluating pathogenicity of variants associated with the long QT syndrome.

Authors:  Jonathan R Kaltman; Frank Evans; Yi-Ping Fu
Journal:  J Cardiovasc Electrophysiol       Date:  2017-11-01

9.  Position of premature termination codons determines susceptibility of hERG mutations to nonsense-mediated mRNA decay in long QT syndrome.

Authors:  Qiuming Gong; Matthew R Stump; Zhengfeng Zhou
Journal:  Gene       Date:  2014-02-13       Impact factor: 3.688

10.  Variant panorama in 1,385 index patients and sensitivity of expanded next-generation sequencing panels in arrhythmogenic disorders.

Authors:  Christoph Marschall; Alexander Moscu-Gregor; Hanns-Georg Klein
Journal:  Cardiovasc Diagn Ther       Date:  2019-10
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