Division of Cardiovascular Medicine

Sampson's Research

Overview

Abdominal Aortic Aneurysm (AAA) is associated with inflammatory cell infiltrate and enzymatic degradation of the vessel wall.  Current diagnostic modalities stratify risk of AAA rupture based solely on the size of the aneurysm without factoring potentially useful information derivable from the degree of aneurysmal wall molecular response.  However, recent developments in imaging technology offer some enticing prospects, including molecular imaging of aneurysmal disease, grouping individuals by the probability that they will develop symptoms or progression, assessing the results of treatment and improving the current understanding of the biology of  AAA.

Research in our lab is centered on the use of noninvasive imaging methods for in vivo structural and molecular assessment of AAA using angiotensin II-induced model of AAA in hyperlipidemic mice in effort to provide further insights on the pathobiology of  AAA and the effects of intervention while eliminating the need to sacrifice and assay animals at individual time points.

Atherosclerosis is a prime predisposing factor for AAA and other cardiovascular diseases.  Consequently, another objective of our research laboratory is to employ multimodiality in vivo imaging methods to delineate the anatomic, cellular, and molecular characteristics of atherosclerosis as the basis for evaluation of interventions and disease progression or risk of complications.

Abstracts/Publications

 
·       Uchechukwu Sampson, Prudhvidhar Perati, Petra Prins, Wellington Pham, Zhouwen Liu, Frank Harrell, Jr, MacRae Linton, John Gore, Valentina Kon, and Sergio Fazio. Quantitative estimates of variability of in vivo ultrasound imaging measurements of mouse aorta important for studies of abdominal aortic aneurysms and related arterial diseases. (In press) Journal of Ultrasound in Medicine 2011
 
·       Uchechukwu K. Sampson, Sergio Fazio, Prudhvidhar R. Perati, Petra Prins, Wellington Pham, Valentina Kon, John C. Gore. In vivo imaging of aneurysmal and non-aneurysmal aortae and iliac arteries in apolipoprotein E knockout mice: accuracy and validation of a new-generation ultrasound micro-imaging system. Arterioscler Thromb Vasc Biol 2010 Scientific Sessions
 
·       Petra Prins, Prudhvidhar R. Perati, Valentina Kon, Sergio Fazio, Lee Limbird, Zhongmao Guo, Uchechukwu K. Sampson. Benzo[a]pyrene Potentiates Angiotensin II-induced Abdominal Aortic Aneurysms in Apolipoprotein E Knockout Mice. Arterioscler Thromb Vasc Biol 2010 Scientific Sessions
 
·       Uchechukwu K. Sampson, Sergio Fazio, Prudhvidhar R. Perati, Petra Prins, Yasin Kokoye, Wellington Pham, Lee Limbird, John C. Gore, Valentina Kon. New insights from in vivo temporal evaluation of angiotensin II-induced abdominal aortic aneurysms in apolipoprotein E knockout mice. Arterioscler Thromb Vasc Biol 2010 Scientific Sessions
 
·       Petra Prins, Prudhvidhar R. Perati, Aramandla Ramesh, Zhongmao Guo, Uchechukwu K. Sampson. Benzo[a]pyrene augments inflammatory and proteolytic changes in mouse model of Abdominal Aortic Aneurysm. Society of Toxicology 50th Annual Meeting and ToxExpo 2011 
 

·      Uchechukwu K.A. Sampson, Sergio Fazio, John W. Patton, Anne-Sophie Sillesen, Amanda K. Wake, Andre L. Churchwell, Alfred S. Callahan. The Potential Role of Carotid Artery Intima-Media Thickness (CIMT) Accretion Rate in Evaluating Risk of Early Atherogenesis. J Am. Coll. Cardiol 2010;55 (10, Supplement A), A142: 1054-340

 

 

 

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