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 PS188. Is Oxidative Stress Important in AAA Pathogenesis?

​Sigitas Urbonavicius1, Grazina Urbonaviciene2, Jes Sandermann1
1Department of Vascular surgery, Regionshospital Midt, Viborg, Denmark; 2Department of Internal medicine, Regionshospital Midt, Silkeborg, Denmark.

OBJECTIVES: Active investigations continue to identify markers other than size that would predict a risk of AAA rupture. Circulating biomarkers could also indicate optimal intervals between the surveillance intervals. Finally, the identification of biomarkers also may identify potential pathogenic pathways, and thus may open possibilities for pharmacological inhibition of growth. In the search of novel biomarkers of AAA progression, serum and wall material proteins were analyzed by a differential proteomic approach.

METHODS: Same layers of AAA wall from ruptured (rAAA) and non-ruptured AAA were incubated, and the proteins released were analyzed by 2-dimensional difference in-gel electrophoresis. Proteins from serum were analyzed and correlated with AAA annual expansion rate.
RESULTS: Several differentially expressed proteins involved in main AAA pathological mechanisms (proteolysis, oxidative stress and thrombosis) were identified by mass spectrometry. Among the proteins identified, peroxiredoxin-2 (PRX-2) was more permanent, which was further validated by Western blot and immunohistochemistry. We demonstrated increased PRX-2 serum levels in rAAA patient wall material compared with AAA subjects and also positive correlation in serum among PRX-2 and AAA diameter and annual expansion rate. Finally, a prospective study revealed a positive correlation between PRX-2 serum levels and AAA expansion rate.
CONCLUSIONS: Several proteins associated with AAA pathogenesis have been identified by a proteomic approach. Protein profiles identified in the serum would appear to be a convenient monitoring tool that has the ability to be both sensitive and specific for AAAs. PRX-2 serum levels are increased in rAAA patients and correlate with AAA size and growth rate, suggesting the potential use of PRX-2 as a biomarker for AAA evolution.
AUTHOR DISCLOSURES: J. Sandermann: Nothing to disclose; G. Urbonaviciene: Nothing to disclose; S. Urbonavicius: Nothing to disclose.
Posted April 2013

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