Systemic vascular inflammation in abdominal aortic aneurysm patients: a contrast-enhanced PET/CT study

• Published in: The quarterly journal of nuclear medicine and molecular imaging Vol. 58; no. 3; pp. 299 - 309
• Main Authors: Morbelli, S, Ghigliotti, G, Spinella, G, Marini, C, Bossert, I, Cimmino, M, Pane, B, Rousas, N, Cittadini, G, Massollo, M, Camellino, D, Riondato, M, Palombo, D, Barisione, C, Sambuceti, G
• Format: Journal Article
• Language: English
• Published: Italy Edizioni Minerva Medica 01-09-2014
• Subjects: Aged; Aortic Aneurysm, Abdominal - blood; Aortic Aneurysm, Abdominal - complications; Aortic Aneurysm, Abdominal - diagnosis; Atherosclerosis; Biomarkers; Biomarkers - blood; Contrast Media; Female; Fluorodeoxyglucose F18; Glucose; Humans; Male; Metabolism; Middle Aged; Multimodal Imaging - methods; Positron-Emission Tomography - methods; Proteins; Radiopharmaceuticals; Regression analysis; Reproducibility of Results; Risk factors; Sensitivity and Specificity; Systemic Vasculitis - blood; Systemic Vasculitis - diagnosis; Systemic Vasculitis - etiology; Tomography, X-Ray Computed - methods
• ISSN: 1824-4785; 1827-1936

The aim of this paper was to investigate the presence of systemic vascular inflammation and its relationship with risk factors and biomarkers of systemic inflammation related to atherosclerosis in asymptomatic abdominal aortic aneurysm (AAA) patients.
Thirty AAA patients and 30 age-matched controls underwent contrast-enhanced 2-deoxy-2-[18F]fluoro-D-glucose (FDG) PET/CT. C-reactive protein, erythrocyte sedimentation rate, white blood cell count and differential, serum fibrinogen, D-dimer and full lipid panel were also evaluated. Region of interest analyses were performed to obtain target-to-background (TBR) metabolism of aorta, subclavian, carotid, iliac arteries and AAA. CT-based arterial calcium load (CL) was evaluated. Arterial Metabolism and CL intergroup differences were tested (unpaired t-test). Linear regression analysis was performed only between blood biomarkers on one side and both TBR and ACL of the arterial districts that resulted significantly different between patients and controls on the other. In all the analyses P values <0.05 were considered significant.
FDG-uptake was higher with respect to controls in aorta, carotid and iliac arteries (P<0.01, P<0.007, P<0.04 respectively). AAA and aorta metabolism showed an inverse correlation with HDL-chol (P<0.02 and P<0.01, respectively) while only aorta showed a direct correlation with lymphocytes' count (P<0.02). Carotid metabolism was directly correlated with monocytes' count and C-reactive protein concentration (P<0.02 and P<0.004, respectively).
The present findings support the relevance of systemic vascular inflammation in all phases of atherosclerosis-related disorders. Moreover they confirm the concept that acute ischemic syndromes might represent the local result of a systemic inflammation rather than the focal involvement of a single arterial lesion.