MMP-9 microsatellite polymorphism and susceptibility to carotid arteries atherosclerosis

被引:40
作者
Fiotti, N
Altamura, N
Fisicaro, M
Carraro, N
Uxa, L
Grassi, G
Torelli, L
Gobbato, R
Guarnieri, G
Baxter, BT
Giansante, C
机构
[1] Univ Trieste, UCO Clin Med Gen & Terapia Med, Dipartimento Sci Clin Morfol & Tecnol, I-34149 Trieste, Italy
[2] ASS 1 Triestina, Ctr Cardiovasc, Trieste, Italy
[3] Univ Trieste, UCO Neurol, Dipartimento Med Clin & Neurol, I-34149 Trieste, Italy
[4] ASS 1 Triestina, Ctr Blood Transfus, Trieste, Italy
[5] Univ Trieste, Dept Math & Informat, I-34149 Trieste, Italy
[6] Univ Nebraska Med Ctr, Dept Surg, Omaha, NE USA
关键词
atherosclerosis; carotid arteries; MMP-9; polymorphism; stroke;
D O I
10.1161/01.ATV.0000219233.31702.c9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective - The aims of this study were to compare a microsatellite polymorphism ( PM) of matrix metalloproteinase (MMP)-9 in patients with carotid atherosclerosis and control population, and to assess the relationship between this PM and plaque structure. Methods and Results - One hundred fifty patients referring to vascular diagnostic centers for suspected carotid atherosclerosis (at ultrasound examination: 110 positive, 40 negative) and controls (n = 110) have been genotyped for MMP-9 PM. After controlling for risk factors, allelic and genotype frequencies were significantly different among the groups, with significant prevalence of long microsatellites in patients with carotid atherosclerosis. Long microsatellites (settled as 22 to 27 repeats) were associated with carotid atherosclerosis (odds ratio [OR], 5.2; 95% confidence interval [CI], 2.9 to 9.2), compared with controls; an independent case control study on patients with coronary atherosclerosis confirmed such result. Binary logistic regression showed that hypertension, long microsatellites in MMP-9 PM and smoking habits were variables accounting for the difference between ultrasound-positive patients and controls. Long microsatellites were also associated to plaques with thin fibrous cap and echolucent core (OR, 13.1; 95% CI, 1.6 to 100). These alleles were slightly more represented in female patients (chi(2) test = 0.019; OR, 2.7; 95% CI, 1.2 to 6) but not associated with other risk factors. Plasma MMP-9 levels were related neither to MMP-9 PM nor to plaque type, and were related to gender and extension of atherosclerosis in carotid arteries. Conclusions - The number of repeats (>= 22 CA) in the microsatellite of MMP- 9 promoter, but not MMP-9 plasma levels, is associated to carotid atherosclerosis and particularly to plaques with a thin fibrous cap.
引用
收藏
页码:1330 / 1336
页数:7
相关论文
共 35 条
[1]   Plasma concentrations and genetic variation of matrix metalloproteinase 9 and prognosis of patients with cardiovascular disease [J].
Blankenberg, S ;
Rupprecht, HJ ;
Poirier, O ;
Bickel, C ;
Smieja, M ;
Hafner, G ;
Meyer, J ;
Cambien, F ;
Tiret, L .
CIRCULATION, 2003, 107 (12) :1579-1585
[2]   IDENTIFICATION OF 92-KD GELATINASE IN HUMAN CORONARY ATHEROSCLEROTIC LESIONS - ASSOCIATION OF ACTIVE ENZYME-SYNTHESIS WITH UNSTABLE ANGINA [J].
BROWN, DL ;
HIBBS, MS ;
KEARNEY, M ;
LOUSHIN, C ;
ISNER, JM .
CIRCULATION, 1995, 91 (08) :2125-2131
[3]   Atherosclerotic plaque rupture in symptomatic carotid artery stenosis [J].
Carr, S ;
Farb, A ;
Pearce, WH ;
Virmani, R ;
Yao, JST .
JOURNAL OF VASCULAR SURGERY, 1996, 23 (05) :755-765
[4]   Matrix metalloproteinase-9 is necessary for the regulation of smooth muscle cell replication and migration after arterial injury [J].
Cho, A ;
Reidy, MA .
CIRCULATION RESEARCH, 2002, 91 (09) :845-851
[5]   Regression of hypertrophied rat pulmonary arteries in organ culture is associated with suppression of proteolytic activity, inhibition of tenascin-C, and smooth muscle cell apoptosis [J].
Cowan, KN ;
Jones, PL ;
Rabinovitch, M .
CIRCULATION RESEARCH, 1999, 84 (10) :1223-1233
[6]   Towards understanding acute destabilization of vulnerable atherosclerotic plaques [J].
Dickson, BC ;
Gotleib, AI .
CARDIOVASCULAR PATHOLOGY, 2003, 12 (05) :237-248
[7]   Targeted deletion of matrix metalloproteinase-9 attenuates left ventricular enlargement and collagen accumulation after experimental myocardial infarction [J].
Ducharme, A ;
Frantz, S ;
Aikawa, M ;
Rabkin, E ;
Lindsey, M ;
Rohde, LE ;
Schoen, FJ ;
Kelly, RA ;
Werb, Z ;
Libby, P ;
Lee, RT .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (01) :55-62
[8]   MMP-9 microsatellite polymorphism: Association with the progression of intima-media thickening and constrictive remodeling of carotid atherosclerotic plaques [J].
Fiotti, N ;
Altamura, N ;
Fisicaro, M ;
Carraro, N ;
Adovasio, R ;
Sarra, VM ;
Uxa, L ;
Guarnieri, G ;
Baxter, BT ;
Giansante, C .
ATHEROSCLEROSIS, 2005, 182 (02) :287-292
[9]   Association of a decreased number of d(CA) repeats in the matrix metalloproteinase-9 promoter with glomerulosclerosis susceptibility in mice [J].
Fornoni, A ;
Wang, YC ;
Lenz, O ;
Striker, LJ ;
Striker, GE .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2002, 13 (08) :2068-2076
[10]   Targeted disruption of the matrix metalloproteinase-9 gene impairs smooth muscle cell migration arterial remodeling and geometrical [J].
Galis, ZS ;
Johnson, C ;
Godin, D ;
Magid, R ;
Shipley, JM ;
Senior, RM ;
Ivan, E .
CIRCULATION RESEARCH, 2002, 91 (09) :852-859