Rare Genetic Variants Associated With Sudden Cardiac Death in Adults

Amit V Khera1, Heather Mason-Suares2, Deanna Brockman3

  • 1Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts; Cardiology Division, Massachusetts General Hospital, Boston, Massachusetts; Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.

Insights

Rare genetic variants are linked to sudden cardiac death in adults. Approximately 1% of asymptomatic individuals carry these potentially dangerous variants, highlighting the importance of genetic screening.

Area of Science:

  • Cardiovascular Genetics
  • Genomics
  • Sudden Cardiac Death Etiology

Background:

  • Sudden cardiac death (SCD) affects numerous U.S. adults annually, often without prior symptoms or diagnosis.
  • Rare pathogenic DNA variants in specific genes predispose individuals to SCD causes like cardiomyopathy and inherited arrhythmias.

Purpose of the Study:

  • To determine the prevalence of rare pathogenic variants in SCD cases versus controls.
  • To assess the prevalence and clinical significance of these mutations in asymptomatic adults.

Main Methods:

  • Whole-exome sequencing was performed on 600 SCD cases and 600 matched controls.
  • Whole-genome sequencing was used in 4,525 asymptomatic adults to evaluate variant prevalence and cardiovascular death risk.

Main Results:

  • 14 pathogenic/likely pathogenic variants were identified in 15 SCD cases (2.5%), but none in controls (p < 0.0001).
  • In asymptomatic adults, 0.9% carried such variants, associated with a 3.24-fold increased risk of cardiovascular death (p=0.02).

Conclusions:

  • Gene sequencing reveals pathogenic variants in a small subset of SCD adults.
  • These variants are found in approximately 1% of asymptomatic adults, indicating potential clinical importance.
Abstract

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