Circulating Lipoprotein-associated Phospholipase A2 in High-grade Carotid Stenosis: A New Biomarker for Predicting Unstable Plaque

Abstract Objective To test plasma levels of lipoprotein-associated phospholipase A2 (Lp-PLA2) in patients with high-grade carotid stenosis according to plaque histology. Methods This cross-sectional single-centre study included patients with ≥70% North American Symptomatic Carotid Endarterectomy Tri...

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Veröffentlicht in:European journal of vascular and endovascular surgery 2012-02, Vol.43 (2), p.154-159
Hauptverfasser: Sarlon-Bartoli, G, Boudes, A, Buffat, C, Bartoli, M.A, Piercecchi-Marti, M.D, Sarlon, E, Arnaud, L, Bennis, Y, Thevenin, B, Squarcioni, C, Nicoli, F, Dignat-George, F, Sabatier, F, Magnan, P.E
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Sprache:eng
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Zusammenfassung:Abstract Objective To test plasma levels of lipoprotein-associated phospholipase A2 (Lp-PLA2) in patients with high-grade carotid stenosis according to plaque histology. Methods This cross-sectional single-centre study included patients with ≥70% North American Symptomatic Carotid Endarterectomy Trial (NASCET) carotid stenosis, who were treated surgically. Serum Lp-PLA2 and high-sensitivity C-reactive protein (hs-CRP) were determined on the day of surgery. Histopathological analysis classified carotid plaque as stable or unstable, according to AHA classification. Results Of the 42 patients (mean age 70.4 ± 10.5 years; 67% men), neurological symptoms were present in 16 (38%). Unstable plaques were found in 23 (55%). Median plasma level of Lp-PLA2 was significantly higher in patients with unstable plaque compared to those with stable plaque (222.4 (174.9–437.5) interquartile range (IQR) 63.5 vs. 211.1 (174.9–270.6) IQR 37.2 ng ml−1 ; p  = 0.02). Moreover, median Lp-PLA2 level were higher in asymptomatic patients with unstable plaque (226.8 ng ml−1 (174.9–437.5) IQR 76.8) vs. stable plaque (206.9 ng ml−1 (174.9–270.6) IQR 33.7; p  = 0.16). Logistic regression showed that only the neurological symptoms (OR = 30.9 (3.7–244.6); p  
ISSN:1078-5884
1532-2165
DOI:10.1016/j.ejvs.2011.10.009