Literature DB >> 19426607

Gender differences in abdominal aortic aneurysms.

Kevin K Hannawa1, Jonathan L Eliason, Gilbert R Upchurch.   

Abstract

Abdominal aortic aneurysms (AAAs) comprise the tenth leading cause of death in Caucasian males 65 to 74 years of age and accounted for nearly 16,000 deaths overall in 2000. Therefore, understanding the pathophysiology of AAAs is an important undertaking. Clinically, multiple risk factors are associated with the development of AAAs, including increasing age, positive smoking history, and hypertension. Male gender is also a well-established risk factor for the development of an AAA, with a 4:1 male to female ratio. The reason for this gender disparity is unknown. The pathogenesis of AAAs formation is complex and multifactorial. Histologically, AAAs are characterized by early chemokine-driven leukocyte infiltration into the aortic wall. Subsequent destruction of elastin and collagen in the media and adventitia ensues owing to excessive local production of matrix-degrading enzymes and is accompanied by smooth muscle cell loss and thinning of the aortic wall. At present, no medical therapies are available to treat patients with aortic aneurysms, using only the crude measurement of aortic diameter as a threshold for which patients must undergo life-threatening and costly surgery. Defining the early mechanisms underlying gender-related differences in AAA formation is critical as understanding differences in disease patterns based on gender may allow us to develop new translational approaches to the prevention and treatment of patients with aortic aneurysms.

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Year:  2009        PMID: 19426607      PMCID: PMC2913052          DOI: 10.2310/6670.2008.00092

Source DB:  PubMed          Journal:  Vascular        ISSN: 1708-5381            Impact factor:   1.285


  93 in total

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4.  Sex-Based Differences Among Experimental Swine Abdominal Aortic aneurysms.

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7.  Monosomy X in Female Mice Influences the Regional Formation and Augments the Severity of Angiotensin II-Induced Aortopathies.

Authors:  Yasir AlSiraj; Sean E Thatcher; Eric Blalock; Wesley N Saintilnord; Alan Daugherty; Hong S Lu; Wei Luo; Ying H Shen; Scott A LeMaire; Arthur P Arnold; Lisa A Cassis
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8.  Vinpocetine protects against the development of experimental abdominal aortic aneurysms.

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9.  Cell sex affects extracellular matrix protein expression and proliferation of smooth muscle progenitor cells derived from human pluripotent stem cells.

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10.  Deficiency in Aim2 affects viability and calcification of vascular smooth muscle cells from murine aortas and angiotensin-II induced aortic aneurysms.

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