Plasma profiling by a protein array approach identifies IGFBP-1 as a novel biomarker of abdominal aortic aneurysm

被引:30
|
作者
Ramos-Mozo, P. [1 ]
Rodriguez, C. [3 ]
Pastor-Vargas, C. [2 ]
Blanco-Colio, L. M. [1 ]
Martinez-Gonzalez, J. [3 ]
Meilhac, O. [5 ]
Michel, J-B [5 ]
Vega de Ceniga, M. [4 ]
Egido, J. [1 ]
Martin-Ventura, J. L. [1 ]
机构
[1] Diaz Autonoma Univ, Vasc Res Lab, Madrid, Spain
[2] Diaz Autonoma Univ, Immunol Lab, IIS Fdn Jimenez, Madrid, Spain
[3] IIB St Pau, Ctr Invest Cardiovasc, Consejo Super Invest Cient, Inst Catalia Ciencies Cardiovasc, Barcelona, Spain
[4] Hosp Galdakao Usansolo, Bilbao, Spain
[5] Univ Paris 07, INSERM, CHU X Bichat, U698, Paris, France
关键词
Biomarkers; Platelets; Thrombosis; Abdominal aortic aneurysm; GROWTH-FACTOR-I; FACTOR-BINDING PROTEIN-1; IGF-I; AGGREGATION; PLATELETS; RELEASE;
D O I
10.1016/j.atherosclerosis.2012.01.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Cytokines are important mediators of immune-inflammatory responses implicated in abdominal aortic aneurysm (AAA) pathogenesis. Our objective was to investigate the cytokine expression profile in plasma of AAA patients. Methods: Cytokine protein expression was measured in plasma of 5 large AAA patients (aortic size > 50 mm) and 5 controls (aortic size <30 mm) using a 20-cytokine antibody-based protein array. IGFBP-1 plasma concentrations were analyzed by ELISA. IGFBP-1 protein levels were analyzed in AAA thrombus by immunohistochemistry and Western blot. Platelet aggregation was assessed by conventional optical aggregometry. Results: Several proteins including MIP-3alpha (CCL20), Eotaxin-2 and IGFBP-1 were increased in AAA patients compared to controls. Among them, IGFBP-1 concentrations were significantly higher in large AAA patients vs control subjects. These data were validated in plasma of patients with large AAA (n = 30) compared to matched controls (n = 30) [ 834(469-1628) vs 497(204-893) pg/ml, p < 0.01]. Furthermore, the potential association of IGFBP-1 with AAA size was analyzed in a second independent group of subjects [ large AAA (n = 59), small AAA patients (aortic size = 30-50 mm, n = 54) and controls (n = 30)]. Interestingly, IGFBP-1 levels correlated with AAA size (r = 0.4, p < 0.001), which remained significant after adjusting for traditional risk factors. IGFBP-1 was localized in the luminal part of AAA thrombus and IGFBP-1 levels were increased in AAA thrombus conditioned media compared to media layer and healthy media. Interestingly, IGFBP-1 abrogated the potentiation of ADP-induced platelet aggregation triggered by IGF-1. Conclusions: IGFBP-1 has been identified by a protein array approach as a potential novel biomarker of AAA. The biological role of IGFBP-1 in AAA pathogenesis could be related to the modulation on the effect of IGF-1 on platelet aggregation. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:544 / 550
页数:7
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