Literature DB >> 24631775

Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths.

Dawei Wang1, Krunal R Shah1, Sung Yon Um1, Lucy S Eng1, Bo Zhou1, Ying Lin1, Adele A Mitchell2, Leze Nicaj3, Mechthild Prinz4, Thomas V McDonald5, Barbara A Sampson3, Yingying Tang6.   

Abstract

Sudden unexplained deaths (SUD) in apparently healthy individuals, for which the causes of deaths remained undetermined after comprehensive forensic investigations and autopsy, present vexing challenges to medical examiners and coroners. Cardiac channelopathies, a group of inheritable diseases that primarily affect heart rhythm by altering the cardiac conduction system, have been known as one of the likely causes of SUD. Adhering to the recommendations of including molecular diagnostics of cardiac channelopathies in SUD investigation, the Molecular Genetics Laboratory of the New York City (NYC) Office of Chief Medical Examiner (OCME) has been routinely testing for six major channelopathy genes (KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2, and RyR2) since 2008. Presented here are the results of cardiac channelopathy testing in 274 well-characterized autopsy negative SUD cases, all with thorough medicolegal death investigation including complete autopsy by NYC OCME between 2008 and 2012. The cohort consisted of 141 infants (92.9% younger than six-month old) and 133 non-infants (78.2% were between 19 and 58 years old). Among the ethnically diverse cohort, African American infants had the highest risks of SUD, and African American non-infants died at significantly younger age (23.7 years old, mean age-at-death) than those of other ethnicities (30.3 years old, mean age-at-death). A total of 22 previously classified cardiac channelopathy-associated variants and 24 novel putative channelopathy-associated variants were detected among the infants (13.5%) and non-infants (19.5%). Most channelopathy-associated variants involved the SCN5A gene (68.4% in infants, 50% in non-infants). We believe this is the first study assessing the role of cardiac channelopathy genes in a large and demographically diverse SUD population drawn from a single urban medical examiner's office in the United States. Our study supports that molecular testing for cardiac channelopathy is a valuable tool in SUD investigations and provides helpful information to medical examiners/coroners seeking cause of death in SUD as well as potentially life-saving information to surviving family members. Published by Elsevier Ireland Ltd.

Entities:  

Keywords:  Arrhythmia; Epidemiology; Genetics testing; Ion channels; Sudden death

Mesh:

Substances:

Year:  2014        PMID: 24631775     DOI: 10.1016/j.forsciint.2014.01.014

Source DB:  PubMed          Journal:  Forensic Sci Int        ISSN: 0379-0738            Impact factor:   2.395


  20 in total

1.  Feasibility of analysis of the SCN5A gene in paraffin embedded samples in sudden infant death cases at the Pretoria Medico-Legal Laboratory, South Africa.

Authors:  Barbara Ströh van Deventer; Lorraine du Toit-Prinsloo; Chantal van Niekerk
Journal:  Forensic Sci Med Pathol       Date:  2018-06-16       Impact factor: 2.007

Review 2.  A Systematic Review of Molecular Autopsy Studies in Sudden Infant Death Cases.

Authors:  Laura Jane Heathfield; Lorna Jean Martin; Raj Ramesar
Journal:  J Pediatr Genet       Date:  2018-08-18

3.  Functional characterization of SCN10A variants in several cases of sudden unexplained death.

Authors:  Ivan Gando; Nori Williams; Glenn I Fishman; Barbara A Sampson; Yingying Tang; William A Coetzee
Journal:  Forensic Sci Int       Date:  2019-05-29       Impact factor: 2.395

Review 4.  Genetic Testing in Inherited Heart Diseases: Practical Considerations for Clinicians.

Authors:  Melanie Care; Vijay Chauhan; Danna Spears
Journal:  Curr Cardiol Rep       Date:  2017-08-16       Impact factor: 2.931

Review 5.  Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?

Authors:  Georgia Sarquella-Brugada; Oscar Campuzano; Sergi Cesar; Anna Iglesias; Anna Fernandez; Josep Brugada; Ramon Brugada
Journal:  Int J Legal Med       Date:  2016-02-12       Impact factor: 2.686

6.  Cardiac Evaluation of Children With a Family History of Sudden Death.

Authors:  Gregory Webster; Rachael Olson; Zachary J Schoppen; Nicholas Giancola; Lauren C Balmert; Sara Cherny; Alfred L George
Journal:  J Am Coll Cardiol       Date:  2019-08-13       Impact factor: 24.094

7.  Infant sudden death: Mutations responsible for impaired Nav1.5 channel trafficking and function.

Authors:  Ivan Gando; Jace Morganstein; Kundan Jana; Thomas V McDonald; Yingying Tang; William A Coetzee
Journal:  Pacing Clin Electrophysiol       Date:  2017-05-16       Impact factor: 1.976

8.  Functional characterization of ABCC9 variants identified in sudden unexpected natural death.

Authors:  Ekaterina Subbotina; Hua-Qian Yang; Ivan Gando; Nori Williams; Barbara A Sampson; Yingying Tang; William A Coetzee
Journal:  Forensic Sci Int       Date:  2019-02-27       Impact factor: 2.395

9.  Practical tips to using formalin-fixed paraffin-embedded tissue archives for molecular diagnostics in a South African setting.

Authors:  Barbara S van Deventer; Lorraine du Toit-Prinsloo; Chantal van Niekerk
Journal:  Afr J Lab Med       Date:  2022-06-23

10.  A de novo BRPF1 variant in a case of Sudden Unexplained Death in Childhood.

Authors:  Christine Keywan; Ingrid A Holm; Annapurna Poduri; Catherine A Brownstein; Sanda Alexandrescu; Jennifer Chen; Christopher Geffre; Richard D Goldstein
Journal:  Eur J Med Genet       Date:  2020-07-08       Impact factor: 2.708

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.