Molecular genetic mechanisms of dilated cardiomyopathy

Curr Opin Genet Dev. 2022 Oct:76:101959. doi: 10.1016/j.gde.2022.101959. Epub 2022 Jul 20.

Abstract

Heart failure (HF) is a rapidly growing cardiovascular condition with a prevalence of ~40 million individuals worldwide [1]. While HF can be caused by acquired conditions such as myocardial infarctions and viruses [2], the genetic basis for HF is rapidly emerging particularly for dilated cardiomyopathy (DCM) that is the most prevalent HF type. In this review, insights from the rapid expansion in next-generation sequencing technologies applied in the HF clinic are merged with recent functional genomics studies to provide a contemporary view of DCM molecular genetics.

Publication types

  • Review
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cardiomyopathy, Dilated* / complications
  • Cardiomyopathy, Dilated* / genetics
  • Genomics
  • Heart Failure* / genetics
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Molecular Biology