Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 2008;117:130
doi: 10.1161/CIRCULATIONAHA.107.188572
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Upchurch, G. R.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Upchurch, G. R., Jr
Related Collections
Right arrow Health policy and outcome research
Right arrow Animal models of human disease
Right arrow Other Treatment
Right arrow CV surgery: aortic and vascular disease
Right arrow Genetics of cardiovascular disease

(Circulation. 2008;117:130.)
© 2008 American Heart Association, Inc.


Editor's Note

Editor’s Note

Gilbert R. Upchurch, Jr, MD

Series Editor, Aortic Diseases


An extract of the first 250 words of the full text is provided, because this article has no abstract.
 

Diseases of the aorta are the 14th leading cause of death in the United States. This complex group of diseases (aneurysms, dissections, and occlusive disease) affects multiple vascular beds, from the aortic valve to the terminal aorta and iliac arteries. Because of this fact, the clinical management of aortic diseases is performed by a variety of healthcare providers.

The incidence and prevalence of aortic disease are increasing as society ages and contributing risk factors go untreated. Thus, these diseases are not rare and, if they are left untreated, patients with aortic disease die. In addition, there are no proven specific or targeted drug therapies to treat aortic disease.

Universal are a significantly higher prevalence in men and a graded increased prevalence with advancing age. The inciting events that lead to aortic disease are not well understood; however, some common themes include: (1) proteolytic derangements in the aortic wall, (2) transmural vessel wall inflammation, (3) immune responses, including a strong genetic link, and (4) altered biomechanical wall stresses along the length of the aorta.

Unfortunately, aortic disease is often clinically silent until patients present with catastrophic aortic rupture or malperfusion of end organs, such as the intestines or kidneys. Alternatively, aortic disease may be discovered serendipitously when healthcare providers perform tests for other disease processes. Discovery of aortic disease before aortic rupture is critical, as there is a huge disparity in mortality rates between patients who undergo aortic repair in the elective setting and those who undergo repair in an emergency . . . [Full Text of this Article]