Pathogenic mechanisms and the potential of drug therapies for aortic aneurysm.


Journal

American journal of physiology. Heart and circulatory physiology
ISSN: 1522-1539
Titre abrégé: Am J Physiol Heart Circ Physiol
Pays: United States
ID NLM: 100901228

Informations de publication

Date de publication:
01 03 2020
Historique:
pubmed: 23 2 2020
medline: 19 5 2020
entrez: 22 2 2020
Statut: ppublish

Résumé

Aortic aneurysm is a permanent focal dilation of the aorta. It is usually an asymptomatic disease but can lead to sudden death due to aortic rupture. Aortic aneurysm-related mortalities are estimated at ∼200,000 deaths per year worldwide. Because no pharmacological treatment has been found to be effective so far, surgical repair remains the only treatment for aortic aneurysm. Aortic aneurysm results from changes in the aortic wall structure due to loss of smooth muscle cells and degradation of the extracellular matrix and can form in different regions of the aorta. Research over the past decade has identified novel contributors to aneurysm formation and progression. The present review provides an overview of cellular and noncellular factors as well as enzymes that process extracellular matrix and regulate cellular functions (e.g., matrix metalloproteinases, granzymes, and cathepsins) in the context of aneurysm pathogenesis. An update of clinical trials focusing on therapeutic strategies to slow abdominal aortic aneurysm growth and efforts underway to develop effective pharmacological treatments is also provided.

Identifiants

pubmed: 32083977
doi: 10.1152/ajpheart.00621.2019
pmc: PMC7099451
doi:

Substances chimiques

Matrix Metalloproteinases EC 3.4.24.-

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

H652-H670

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL088447
Pays : United States
Organisme : Canadian Institutes for Health Research
Pays : International
Organisme : NHLBI NIH HHS
ID : R01 HL122562
Pays : United States

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Auteurs

Bo Liu (B)

University of Wisconsin, Madison, Department of Surgery, Madison Wisconsin.

David J Granville (DJ)

International Collaboration on Repair Discoveries Centre and University of British Columbia Centre for Heart Lung Innovation, Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.

Jonathan Golledge (J)

The Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Department of Vascular and Endovascular Surgery, Townsville Hospital and Health Services, Townsville, Queensland, Australia.

Zamaneh Kassiri (Z)

University of Alberta, Department of Physiology, Cardiovascular Research Center, Faculty of Medicine and Dentistry, Edmonton, Alberta, Canada.

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