ARTERIOSCLEROSIS, THROMBOSIS, AND VASCULAR BIOLOGY
Abstract
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 (n110) 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 (2 test0.019; 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.