Current Cardiology Reports

, Volume 12, Issue 2, pp 99–107

The Pathogenesis of Aortopathy in Marfan Syndrome and Related Diseases

Article

DOI: 10.1007/s11886-010-0083-z

Cite this article as:
Jones, J.A. & Ikonomidis, J.S. Curr Cardiol Rep (2010) 12: 99. doi:10.1007/s11886-010-0083-z

Abstract

Marfan syndrome is a systemic connective tissue disorder that is inherited in an autosomal-dominant pattern with variable penetrance. Although there are many clinical manifestations of this disease, the most life threatening are cardiovascular complications, including mitral valve prolapse and aortic root aneurysm. When the primary defect was discovered in the fibrillin-1 gene, it was hypothesized that mutations in fibrillin-1 resulted in a weakened and disordered elastic architecture. However, recent evidence has suggested that the Marfan syndrome is caused by more than just a disordered microfibril matrix. Interest was stimulated when it was discovered that fibrillin-1 mutations enhanced the release of sequestered latent transforming growth factor-β, a well-described mediator of vascular remodeling. This article focuses on the pathophysiology of aortopathy in the Marfan syndrome and related diseases, with special emphasis on the role of transforming growth factor-β in mediating the pathogenesis of this disease.

Keywords

Marfan syndrome Aneurysm Transforming growth factor-beta Signaling Clinical treatment 

Copyright information

© Springer Science+Business Media, LLC 2010

Authors and Affiliations

  1. 1.Division of Cardiothoracic SurgeryMedical University of South CarolinaCharlestonUSA

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