Molecular autopsy in Chinese sudden cardiac death in the young

Abstract

Inherited cardiovascular conditions are significant causes of sudden cardiac death in the young (SCDY), making their investigation using molecular autopsy and prevention a public health priority. However, the molecular autopsy data in Chinese population is lacking. The 5‐year result (2017–2021) of molecular autopsy services provided for victims of SCDY (age 1–40 years) was reviewed. The outcome of family cascade genetic screening and clinical evaluation was reviewed. A literature review of case series reporting results of molecular autopsy on SCDY in 2016–2023 was conducted. Among the 41 decedents, 11 were found to carry 13 sudden cardiac death (SCD)‐causative genetic variants. Likely pathogenic (LP) variants were identified in the DSP, TPM1, TTN, and SCN5A genes. Cascade genetic testing identified four family members with LP variants. One family member with familial TPM1 variant was found to have hypertrophic cardiomyopathy upon clinical evaluation. This study provided insight into the genetic profile of molecular autopsy in a Chinese cohort of SCDY. The detection of important SCD‐causative variants through molecular autopsy has facilitated family cascade screening by targeted genetic testing and clinical evaluation of at‐risk family members. A literature review of the current landscape of molecular autopsy in the investigation of SCDY was conducted.