Bicuspid Aortic Valve: Unlocking the Morphogenetic Puzzle

Am J Med. 2016 Aug;129(8):796-805. doi: 10.1016/j.amjmed.2016.03.009. Epub 2016 Apr 6.

Abstract

Although bicuspid aortic valve is the most common congenital abnormality, it is perhaps erroneous to consider this disease one clinical entity. Rather, it may be useful to consider it a cluster of diseases incorporating different phenotypes, etiologies, and pathogenesis. Discussion of bicuspid aortic valve can be difficult because there is no clear consensus on a phenotypic description among authors, and many classification schemes have been proposed. The literature suggests that different phenotypes have different associations and clinical manifestations. In addition, recent studies suggest a genetic basis for the disease, yet few genes have so far been described. Furthermore, recent scientific literature has been focusing on the increased risk of aortic aneurysms, but the pathogenesis of bicuspid aortic valve aortopathy is still unclear. The aim of this paper is to review the current evidence about the unsolved issues around bicuspid aortic valve.

Keywords: Aortic valve disease; Aortopathy; Bicuspid aortic valve.

Publication types

  • Review

MeSH terms

  • Animals
  • Aortic Diseases / etiology
  • Aortic Valve / abnormalities*
  • Aortic Valve / diagnostic imaging
  • Aortic Valve / pathology
  • Bicuspid Aortic Valve Disease
  • Genetic Predisposition to Disease
  • Heart Valve Diseases / complications
  • Heart Valve Diseases / diagnostic imaging
  • Heart Valve Diseases / genetics
  • Heart Valve Diseases / pathology*
  • Humans
  • Phenotype
  • Risk Factors