Association of plasma eotaxin levels with the presence and extent of angiographic coronary artery disease

被引:63
作者
Emanuele, E
Falcone, C
D'Angelo, A
Minoretti, P
Buzzi, MP
Bertona, M
Geroldi, D
机构
[1] Univ Pavia, Interdepartmental Ctr Res Mol Med, CIRMC, I-27100 Pavia, Italy
[2] Univ Pavia, IRCCS San Matteo Hosp, Dept Cardiol, I-27100 Pavia, Italy
[3] Univ Pavia, Dept Internal Med & Med Therapeut, IRCCS San Matteo Hosp, I-27100 Pavia, Italy
关键词
eotaxin; coronary artery disease; angiography; stenosis;
D O I
10.1016/j.atherosclerosis.2005.07.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Eotaxin (CCL 11) is an eosinophil-specific chemoattractant which has been found to be highly expressed at sites of vascular pathology. In the present study, we aimed to evaluate the association of plasma eotaxin levels with the presence and extent of angiographic coronary artery disease (CAD). Three hundred and fifty six consecutive patients attending for elective coronary angiography were investigated. Compared with 111 patients without CAD, 245 with CAD showed higher eotaxin concentrations [median (interquartile range): 76.0 (56.3-103.0) pg/ml versus 116.0 (80.5-162.0) pg/ml, respectively; P < 0.001]. Importantly, a significant Spearman correlation was found between eotaxin levels and the extent score of coronary artery stenosis (r = 0.449, P < 0.001). A stepwise increase in plasma levels of eotaxin was also found depending on the number of > 50% coronary stenosis: median value 76.0 pg/ml in CAD(-) subjects, 96.0 pg/ml in 1-vessel disease, 128.0 pg/ml in 2-vessel disease, and 129.0 pg/ml in 3-vessel disease (P < 0.001 for trend). After confounding variables were controlled for, multiple stepwise regression analysis demonstrated that plasma eotaxin was an independent predictor of angiographic extent of CAD (P = 0.426, P < 0.001). Our data suggest that increased eotaxin levels are associated with the presence of CAD and that circulating levels of this chemokine may reflect the extent of coronary atherosclerosis. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:140 / 145
页数:6
相关论文
共 25 条
[11]   Significance of apolipoprotein(a) phenotypes in acute coronary syndromes: relation with clinical presentation [J].
Emanuele, E ;
Peros, E ;
Minoretti, P ;
D'Angelo, A ;
Montagna, L ;
Falcone, C ;
Geroldi, D .
CLINICA CHIMICA ACTA, 2004, 350 (1-2) :159-165
[12]   THE CHEMOKINE, EOTAXIN, ACTIVATES GUINEA-PIG EOSINOPHILS IN-VITRO AND CAUSES THEIR ACCUMULATION INTO THE LUNG IN-VIVO [J].
GRIFFITHSJOHNSON, DA ;
COLLINS, PD ;
ROSSI, AG ;
JOSE, PJ ;
WILLIAMS, TJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 197 (03) :1167-1172
[13]  
Haley KJ, 2000, CIRCULATION, V102, P2185
[14]   Monocyte chemoattractant protein-1 and coronary artery disease [J].
Ikeda, U ;
Matsui, K ;
Murakami, Y ;
Shimada, K .
CLINICAL CARDIOLOGY, 2002, 25 (04) :143-147
[15]   EOTAXIN - A POTENT EOSINOPHIL CHEMOATTRACTANT CYTOKINE DETECTED IN A GUINEA-PIG MODEL OF ALLERGIC AIRWAYS INFLAMMATION [J].
JOSE, PJ ;
GRIFFITHSJOHNSON, DA ;
COLLINS, PD ;
WALSH, DT ;
MOQBEL, R ;
TOTTY, NF ;
TRUONG, O ;
HSUAN, JJ ;
WILLIAMS, TJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (03) :881-887
[16]   Molecular cloning of human eotaxin, an eosinophil-selective CC chemokine, and identification of a specific eosinophil eotaxin receptor, CC chemokine receptor 3 [J].
Kitaura, M ;
Nakajima, T ;
Imai, T ;
Harada, S ;
Combadiere, C ;
Tiffany, HL ;
Murphy, PM ;
Yoshie, O .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (13) :7725-7730
[17]  
MACHIN D, 1987, STAT TABLE DESIGN CL
[18]  
MOSEDALE DE, 2005, ATHROSCLEROSIS
[19]   Plasma osteopontin levels are associated with the presence and extent of coronary artery disease [J].
Ohmori, R ;
Momiyama, Y ;
Taniguchi, H ;
Takahashi, R ;
Kusuhara, M ;
Nakamura, H ;
Ohsuzu, F .
ATHEROSCLEROSIS, 2003, 170 (02) :333-337
[20]   Cloning of the human eosinophil chemoattractant, eotaxin - Expression, receptor binding, and functional properties suggest a mechanism for the selective recruitment of eosinophils [J].
Ponath, PD ;
Qin, SX ;
Ringler, DJ ;
ClarkLewis, I ;
Wang, J ;
Kassam, N ;
Smith, H ;
Shi, XJ ;
Gonzalo, JA ;
Newman, W ;
GutierrezRamos, JC ;
Mackay, CR .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (03) :604-612