Potential Common Pathogenic Pathways for the Left Ventricular Noncompaction Cardiomyopathy (LVNC)

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

Ventricular trabeculation and compaction are two essential morphogenetic events for generating a functionally competent ventricular wall. A significant reduction in trabeculation is usually associated with hypoplastic wall and ventricular compact zone deficiencies, which commonly leads to embryonic heart failure and early embryonic lethality. In contrast, the arrest of ventricular wall compaction (noncompaction) is believed to be causative to the left ventricular noncompaction (LVNC), a genetically heterogeneous disorder and the third most common cardiomyopathy among pediatric patients. After critically reviewing recent findings from genetically engineered mouse models, we suggest a model which proposes that defects in myofibrillogenesis and polarization in trabecular cardiomyocytes underly the common pathogenic mechanism for ventricular noncompaction.

Original languageEnglish (US)
Pages (from-to)1099-1106
Number of pages8
JournalPediatric Cardiology
Volume39
Issue number6
DOIs
StatePublished - Aug 1 2018

    Fingerprint

Keywords

  • Cardiomyopathy
  • Congenital heart defects
  • Genetic pathway
  • Heart development
  • Ventricular noncompaction

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Cardiology and Cardiovascular Medicine

Cite this