Recent advances in molecular mechanisms of abdominal aortic aneurysm formation

被引:43
作者
Annambhotla, Suman [2 ]
Bourgeois, Sebastian [2 ]
Wang, Xinwen [2 ]
Lin, Peter H. [2 ]
Yao, Qizhi [2 ]
Chen, Changyi [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Surg, Houston, TX 77030 USA
[2] Baylor Coll Med, Mol Surg Res Ctr,Michael DeBakey VA Med Ctr, Div Vasc Surg & Endovasc Therapy, Michael DeBakey Dept Surg, Houston, TX 77030 USA
关键词
D O I
10.1007/s00268-007-9456-x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Abdominal aortic aneurysm (AAA) is an increasingly common clinical condition with fatal implications. It is associated with advanced age, male gender, cigarette smoking, atherosclerosis, hypertension, and genetic predisposition. Although significant evidence has emerged in the last decade, the molecular mechanisms of AAA formation remain poorly understood. Currently, the treatment for AAA remains primarily surgical with the lone innovation of endovascular therapy. With advances in the human genome, understanding precisely which molecules and genes mediate AAA development and blocking their activity at the molecular level could lead to important new discoveries and therapies. This review summarizes recent updates in molecular mechanisms of AAA formation, including animal models, autoimmune components, infection, key molecules and cytokines, mechanical forces, genetics, and pharmacotherapy. This review will be helpful to those who want to recognize the newest endeavors within the field and identify possible lines of investigation in AAA.
引用
收藏
页码:976 / 986
页数:11
相关论文
共 68 条
[1]   Collagen degradation in the abdominal aneurysm -: A conspiracy of matrix metalloproteinase and cysteine collagenases [J].
Abdul-Hussien, Hazem ;
Soekhoe, Ratna G. V. ;
Weber, Ekkehard ;
von der Thuesen, Jan H. ;
Kleemann, Robert ;
Mulder, Adri ;
van Bockel, J. Hajo ;
Hanemaaijer, Roeland ;
Lindeman, Jan H. N. .
AMERICAN JOURNAL OF PATHOLOGY, 2007, 170 (03) :809-817
[2]   ELASTASE-INDUCED EXPERIMENTAL ANEURYSMS IN RATS [J].
ANIDJAR, S ;
SALZMANN, JL ;
GENTRIC, D ;
LAGNEAU, P ;
CAMILLERI, JP ;
MICHEL, JB .
CIRCULATION, 1990, 82 (03) :973-981
[3]   Turning back the clock: regression of abdominal aortic aneurysms via pharmacotherapy [J].
Aoki, Hiroki ;
Yoshimura, Koichi ;
Matsuzaki, Masunori .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2007, 85 (10) :1077-1088
[4]   The role of human leukocyte antigen genes in the formation of abdominal aortic aneurysms [J].
Badger, Stephen A. ;
Soong, Chee V. ;
O'Donnell, Mark E. ;
Middleton, Derek .
JOURNAL OF VASCULAR SURGERY, 2007, 45 (03) :475-480
[5]  
Baxter BT, 1999, J VASC SURG, V29, P138
[6]  
BENGTSSON H, 1992, EUR J SURG, V158, P19
[7]   Pharmacological targets in the treatment of abdominal aortic aneurysms [J].
Bergoeing, Michel P. ;
Thompson, Robert W. ;
Curci, John A. .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2006, 10 (04) :547-559
[8]   The matrix metalloproteinase inhibitor BB-94 limits expansion of experimental abdominal aortic aneurysms [J].
Bigatel, DA ;
Elmore, JR ;
Carey, DJ ;
Cizmeci-Smith, G ;
Franklin, DP ;
Youkey, JR .
JOURNAL OF VASCULAR SURGERY, 1999, 29 (01) :130-138
[9]   The role of cytokine gene polymorphisms in the pathogenesis of abdominal aortic aneurysms: A case-control study [J].
Bown, MJ ;
Burton, PR ;
Horsburgh, T ;
Nicholson, ML ;
Bell, PRF ;
Sayers, RD .
JOURNAL OF VASCULAR SURGERY, 2003, 37 (05) :999-1005
[10]   Aldosterone does not mediate angiotensin II-induced atherosclerosis and abdominal aortic aneurysms [J].
Cassis, LA ;
Helton, MJ ;
Howatt, DA ;
King, VL ;
Daugherty, A .
BRITISH JOURNAL OF PHARMACOLOGY, 2005, 144 (03) :443-448