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Author Notes:

Correspondence: W. Robert Taylor, MD, PhD, Division of Cardiology, Emory University School of Medicine, 101 Woodruff Circle, Suite 319 WMB, Atlanta GA, 30322, Phone 404-727-3754, FAX 404-727- 3858, w.robert.taylor@emory.edu

The authors have no conflicts of interest to disclose.

Subjects:

Research Funding:

This work was supported by a grant from the National Institutes of Health (PO1 HL095070).

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Cardiac & Cardiovascular Systems
  • Hematology
  • Peripheral Vascular Disease
  • Cardiovascular System & Cardiology
  • aneurysm
  • animals
  • aorta
  • models, animal
  • pathophysiology
  • Vascular smooth muscle
  • Nitric oxide synthase
  • Human abdominal aorta
  • CD4(+) T-cells
  • Matrix metalloproteinases
  • Oxidative stress
  • Marfan syndrome
  • Intraluminal
  • Mast cells
  • Signals transduction

Cellular Mechanisms of Aortic Aneurysm Formation

Tools:

Journal Title:

Circulation Research

Volume:

Volume 124, Number 4

Publisher:

, Pages 607-618

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Aortic aneurysms are a common vascular disease in Western populations that can involve virtually any portion of the aorta. Abdominal aortic aneurysms are much more common than thoracic aortic aneurysms and combined they account for >25 000 deaths in the United States annually. Although thoracic and abdominal aortic aneurysms share some common characteristics, including the gross anatomic appearance, alterations in extracellular matrix, and loss of smooth muscle cells, they are distinct diseases. In recent years, advances in genetic analysis, robust molecular tools, and increased availability of animal models have greatly enhanced our knowledge of the pathophysiology of aortic aneurysms. This review examines the various proposed cellular mechanisms responsible for aortic aneurysm formation and identifies opportunities for future studies.

Copyright information:

© 2019 American Heart Association, Inc.

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