4.7 Review

Genetics of Thoracic Aortic Aneurysm: At the Crossroad of Transforming Growth Factor- Signaling and Vascular Smooth Muscle Cell Contractility

Journal

CIRCULATION RESEARCH
Volume 113, Issue 3, Pages 327-340

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCRESAHA.113.300675

Keywords

aortic aneurysm; thoracic; Loeys-Dietz syndrome; Marfan syndrome; TGF- signaling; vascular smooth muscle cell

Funding

  1. Fund for Scientific Research, Flanders (Belgium) [G.0458.09, G.0221.12]
  2. Fondation Leducq
  3. European Research Council

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Aortic aneurysm, including both abdominal aortic aneurysm and thoracic aortic aneurysm, is the cause of death of 1% to 2% of the Western population. This review focuses only on thoracic aortic aneurysms and dissections. During the past decade, the genetic contribution to the pathogenesis of thoracic aortic aneurysms and dissections has revealed perturbed extracellular matrix signaling cascade interactions and deficient intracellular components of the smooth muscle contractile apparatus as the key mechanisms. Based on the study of different Marfan mouse models and the discovery of several novel thoracic aortic aneurysm genes, the involvement of the transforming growth factor- signaling pathway has opened unexpected new avenues. Overall, these discoveries have 3 important consequences. First, the pathogenesis of thoracic aortic aneurysms and dissections is better understood, although some controversy still exists. Second, the management strategies for the medical and surgical treatment of thoracic aortic aneurysms and dissections are becoming increasingly gene-tailored. Third, the pathogenetic insights have delivered new treatment options that are currently being investigated in large clinical trials.

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