Yield of Molecular Autopsy in Sudden Cardiac Death in Athletes. Data from a Large Registry in the United Kingdom.

Molecular autopsy sudden cardiac death

Journal

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
ISSN: 1532-2092
Titre abrégé: Europace
Pays: England
ID NLM: 100883649

Informations de publication

Date de publication:
30 Jan 2024
Historique:
received: 20 10 2023
accepted: 02 01 2024
medline: 30 1 2024
pubmed: 30 1 2024
entrez: 30 1 2024
Statut: aheadofprint

Résumé

Sudden cardiac death (SCD) may occur in apparently healthy individuals, including athletes. We report the diagnostic role of post-mortem genetic testing, molecular autopsy (MA), in elucidating the cause of SCD in athletes. We reviewed a database of 6860 consecutive cases of SCD referred to our specialist cardiac pathology centre. All cases underwent detailed cardiac autopsy and 748 were deemed to be athletes. Of these, 42 (6%) were investigated with MA (28 using a targeted sequencing, 14 exome sequencing). Variants were classified manually as pathogenic (P), likely pathogenic (LP), variant of unknown significance (VUS) using international guidelines. Clinical information was obtained from referring coroners who completed a detailed health questionnaire. Out of the 42 decedents (average age 35 years old, 98% males) who were investigated with MA, the autopsy was in keeping with a structurally normal heart (sudden arrhythmic death syndrome, SADS) in n = 33 (78%) cases, followed by arrhythmogenic cardiomyopathy (ACM) in 8 (19%) individuals and idiopathic left ventricular fibrosis in 1 (2%). Death occurred during exercise and at rest in 26 (62%) and 16 (38%) individuals respectively. Variants that were adjudicated clinically actionable were present in 7 cases (17%). There was concordance between the genetic and phenotypic findings in 2 cases of ACM. None of the variants identified in SADS cases were previously linked to channelopathies. Clinically actionable variants in cardiomyopathy-associated genes were found in 5 cases of SADS. The yield of MA in athletes who died suddenly is 17%. In SADS cases, clinically actionable variants were found in cardiomyopathy-associated genes and not in channelopathy-associated genes. ACM is a common cause of SCD in athletes and one in four decedents had a clinically actionable variant in FLNC and TMEM43 genes.

Sections du résumé

BACKGROUND BACKGROUND
Sudden cardiac death (SCD) may occur in apparently healthy individuals, including athletes. We report the diagnostic role of post-mortem genetic testing, molecular autopsy (MA), in elucidating the cause of SCD in athletes.
METHODS METHODS
We reviewed a database of 6860 consecutive cases of SCD referred to our specialist cardiac pathology centre. All cases underwent detailed cardiac autopsy and 748 were deemed to be athletes. Of these, 42 (6%) were investigated with MA (28 using a targeted sequencing, 14 exome sequencing). Variants were classified manually as pathogenic (P), likely pathogenic (LP), variant of unknown significance (VUS) using international guidelines. Clinical information was obtained from referring coroners who completed a detailed health questionnaire.
RESULTS RESULTS
Out of the 42 decedents (average age 35 years old, 98% males) who were investigated with MA, the autopsy was in keeping with a structurally normal heart (sudden arrhythmic death syndrome, SADS) in n = 33 (78%) cases, followed by arrhythmogenic cardiomyopathy (ACM) in 8 (19%) individuals and idiopathic left ventricular fibrosis in 1 (2%). Death occurred during exercise and at rest in 26 (62%) and 16 (38%) individuals respectively. Variants that were adjudicated clinically actionable were present in 7 cases (17%). There was concordance between the genetic and phenotypic findings in 2 cases of ACM. None of the variants identified in SADS cases were previously linked to channelopathies. Clinically actionable variants in cardiomyopathy-associated genes were found in 5 cases of SADS.
CONCLUSIONS CONCLUSIONS
The yield of MA in athletes who died suddenly is 17%. In SADS cases, clinically actionable variants were found in cardiomyopathy-associated genes and not in channelopathy-associated genes. ACM is a common cause of SCD in athletes and one in four decedents had a clinically actionable variant in FLNC and TMEM43 genes.

Identifiants

pubmed: 38289717
pii: 7592033
doi: 10.1093/europace/euae029
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.

Auteurs

Gherardo Finocchiaro (G)

Cardiovascular Clinical Academic Group and Cardiology Research Section, St. George's, University of London, St. George's University Hospitals NHS Foundation Trust, United Kingdom.

Davide Radaelli (D)

Cardiovascular Clinical Academic Group and Cardiology Research Section, St. George's, University of London, St. George's University Hospitals NHS Foundation Trust, United Kingdom.
Department of Medicine, Surgery and Health, University of Trieste, Trieste, Italy.

David Johnson (D)

Cardiovascular Clinical Academic Group and Cardiology Research Section, St. George's, University of London, St. George's University Hospitals NHS Foundation Trust, United Kingdom.

Raghav T Bhatia (RT)

Cardiovascular Clinical Academic Group and Cardiology Research Section, St. George's, University of London, St. George's University Hospitals NHS Foundation Trust, United Kingdom.

Joseph Westaby (J)

Cardiovascular Clinical Academic Group and Cardiology Research Section, St. George's, University of London, St. George's University Hospitals NHS Foundation Trust, United Kingdom.

Stefano D'Errico (S)

Department of Medicine, Surgery and Health, University of Trieste, Trieste, Italy.

Michael Papadakis (M)

Cardiovascular Clinical Academic Group and Cardiology Research Section, St. George's, University of London, St. George's University Hospitals NHS Foundation Trust, United Kingdom.

Sanjay Sharma (S)

Cardiovascular Clinical Academic Group and Cardiology Research Section, St. George's, University of London, St. George's University Hospitals NHS Foundation Trust, United Kingdom.

Mary N Sheppard (MN)

Cardiovascular Clinical Academic Group and Cardiology Research Section, St. George's, University of London, St. George's University Hospitals NHS Foundation Trust, United Kingdom.

Elijah R Behr (ER)

Cardiovascular Clinical Academic Group and Cardiology Research Section, St. George's, University of London, St. George's University Hospitals NHS Foundation Trust, United Kingdom.

Classifications MeSH