Modifier genes for sudden cardiac death

Peter J. Schwartz*, Lia Crotti, Alfred L. George

*Corresponding author for this work

Research output: Contribution to journalReview article

13 Scopus citations

Abstract

Genetic conditions, even those associated with identical gene mutations, can present with variable clinical manifestations. One widely accepted explanation for this phenomenon is the existence of genetic factors capable of modifying the consequences of disease-causing mutations (modifier genes). Here, we address the concepts and principles by which genetic factors may be involved in modifying risk for cardiac arrhythmia, then discuss the current knowledge and interpretation of their contribution to clinical heterogeneity. We illustrate these concepts in the context of two important clinical conditions associated with risk for sudden cardiac death including a monogenic disorder (congenital long QT syndrome) in which the impact of modifier genes has been established, and a complex trait (life-threatening arrhythmias in acute myocardial infarction) for which the search for genetic modifiers of arrhythmic risk is more challenging. Advances in understanding the contribution of modifier genes to a higher or lower propensity towards sudden death should improve patient-specific risk stratification and be a major step towards precision medicine.

Original languageEnglish (US)
Pages (from-to)3925-3931
Number of pages7
JournalEuropean heart journal
Volume39
Issue number44
DOIs
StatePublished - Nov 21 2018

Keywords

  • Acute myocardial infarction
  • Genetic modifiers
  • Genetic variants
  • Genetics
  • Long QT syndrome

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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