Abstract

BackgroundAortic aneurysm is an increasingly common vascular disorder with fatal implication. However, there is no established diagnosis other than that based on aneurysmal size. For this purpose, serum protein biomarkers for aortic aneurysms are valuable. Although most of the studies on serum biomarker discovery have been based on comparison of serum proteins from the patient group with those from the healthy group, we considered that comparison of serial protein profiles such as those in presurgical and postsurgical sera within one patient would facilitate identification of biomarkers since the variability of serial protein profiles within one patient is smaller than that between groups. In this study, we examined serum proteins with differential levels in postsurgery compared with those in presurgery after the removal of aneurysmal tissues in abdominal aortic aneurysm (AAA) and thoracic aortic aneurysm (TAA) patients in order to identify potential serum biomarkers for AAAs and TAAs.ResultsA proteomic approach with an isobaric tag for relative and absolute quantitation (iTRAQ) labeling followed by nano liquid chromatography (nanoLC)-matrix-assisted laser desorption ionization (MALDI)-time of flight (TOF/TOF)-tandem mass spectrometry (MS/MS) was used. In the sera of patients with AAAs and TAAs, a total of 63 and 71 proteins with differential levels were further narrowed down to 6 and 8 increased proteins (≧1.3 fold, postsurgical vs. presurgical) (p < 0.05, patient vs. control) and 12 and 17 decreased proteins (< 0.77 fold, postsurgical vs. presurgical) (p < 0.05, patient vs. control) in postsurgical sera compared with those in presurgical sera, respectively. All of the increased proteins in postsurgical sera of both AAA and TAA patients included several known acute-phase proteins. On the other hand, in the decreased proteins, we found intriguing molecules such as α-2-macroglobulin, gelsolin, kallistatin, and so on. Among them, we confirmed that kallistatin in both AAA and TAA patients and α-2-macroglobulin in TAA patients showed decrease levels in postsurgical sera similar to those in control sera by Western blot analysis with other sera from AAA and TAA patients.ConclusionsTaken together, our findings suggest that Kallistatin and α-2-macroglobulin are potential serum biomarkers for both AAA and TAA and TAA, respectively.

Highlights

  • Aortic aneurysm is an increasingly common vascular disorder with fatal implication

  • It has been shown that intimal atherosclerosis, chronic transmural inflammation and elastic media destruction are associated with abdominal aortic aneurysm (AAA) growth, but many of thoracic aortic aneurysm (TAA) arise in the absence of atherosclerotic plaque deposition

  • Protein levels in postsurgical sera were compared with those in presurgical sera using isobaric tag for relative and absolute quantitation (iTRAQ) labeling coupled to Nano liquid chromatography (nanoLC)-matrix-assisted laser desorption ionization (MALDI)-Time of flight (TOF)/TOFMS/mass spectrometry (MS) followed by ProteinPilot analysis

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Summary

Introduction

There is no established diagnosis other than that based on aneurysmal size. For this purpose, serum protein biomarkers for aortic aneurysms are valuable. There is no established medical therapeutics for small aneurysms For this purpose, plasma/ serum protein biomarkers are available. Studies are needed to find the serum/plasma biomarkers other than those for diagnosis based on aneurysmal size for the prediction of aneurysmal risk [3]. Proteome profiling of serum could facilitate the discovery of AAA and/or TAA biomarkers for prognosis and therapeutic purposes for patients with aortic aneurysms. It is conceivable that pathological disparities between AAA and TAA would bear different serum/plasma biomarkers related to each aneurysm

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