Sudden Cardiac Death In Persons Aged 50 Years Or Younger: Diagnostic Yield Of A Regional Molecular Autopsy Program Using Massive Sequencing

Tomás Ripoll-Vera, Consuelo Pérez Luengo, Juan Carlos Borondo Alcázar,Ana Belén García Ruiz, Nieves Sánchez Del Valle,Bernardino Barceló Martín, Juan Luis Poncela García, Gloria Gutiérrez Buitrago, Concepción Dasi Martínez, Juan Carlos Canós Villena,Susana Moyano Corvillo, Raquel Esgueva Pallarés, Juan Ramón Sancho Sancho, Gemma Guitart Pinedo, Elena Hernández Marín, Estela García García, Albert Vingut López,Jorge Álvarez Rubio,Nancy Govea Callizo, Yolanda Gómez Pérez, Catalina Melià Mesquida, Damián Heine,Jordi Rosell Andreo,Lorenzo Socías Crespí

REVISTA ESPANOLA DE CARDIOLOGIA(2021)

引用 6|浏览5
暂无评分
摘要
Introduction and objectives: Sudden cardiac death (SCD) in young people often has a genetic cause. Consequently, the results of "molecular autopsy'' may have important implications for their relatives. Our objective was to evaluate the diagnostic yield of a molecular autopsy program using next-generation sequencing.Methods: We performed a prospective study of a cohort of consecutive patients who died from nonviolent SCD, aged <= 50 years, and who underwent molecular autopsy using large panels of next-generation sequencing, with subsequent clinical and genetic family screening. We analyzed demographic, clinical, toxicological, and genetic data.Results: We studied 123 consecutive cases of SCD in persons aged <= 50 years. The incidence of SCD was 5.8 cases/100 000 individuals/y, mean age was 36.15 +/- 12.7 years, and 95 were men (77%). The cause was cardiac in 53%, unexplained SCD in 24%, toxic in 10.6%, and infant SCD in 4%. Among cardiac causes, ischemic heart disease accounted for 38% of deaths, arrhythmogenic cardiomyopathy for 7%, hypertrophic cardiomyopathy for 5%, and idiopathic left ventricular hypertrophy for 11%. Genetic analysis was performed in 62 cases (50.4%). Genetic variants were found in 42 cases (67.7%), with a mean of 3.4 +/- 4 genetic variants/patient, and the variant found was considered to be pathogenic or probably pathogenic in 30.6%. In unexplained SCD, 70% showed some genetic variant. Family screening diagnosed 21 carriers or affected individuals, 5 of whom were at risk, indicating an implantable cardiac defibrillator.Conclusions: Protocol-based and exhaustive study of SCD from cardiac causes in persons aged <= 50 years is feasible and necessary. In a high percentage of cases, the cause is genetic, indicating the existence of relatives at risk who could benefit from early diagnosis and treatment to avoid complications. (C) 2020 Sociedad Espanola de Cardiologia. Published by Elsevier Espana, S.L.U. All rights reserved.
更多
查看译文
关键词
Sudden cardiac death, Genetics, Cardiomyopathies, Channelopathies, Mutations
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要