
PECAM-1 GENE POLYMORPHISM (rs668) AND SUBCLINICAL
MARKERS OF CAROTID ATHEROSCLEROSIS IN PATIENTS
WITH TYPE 2 DIABETES MELLITUS Popović D, Nikolajević Starčević J, Šantl Letonja M, Makuc J,
Cokan Vujkovac A, Reschner H, Bregar D, Petrovič D *Corresponding Author: Professor Daniel Petrovič, M.D., Ph.D., Institute of Histology and Embryology,
Faculty of Medicine University Ljubljana, Korytkova 2, SI-1000 Ljubljana, Slovenia. Tel: +386-1-543-7367.
Fax: +386-1-543-7361. E-mail: daniel.petrovic@mf.uni-lj.si page: 63
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RESULTS
The clinical characteristics of subjects with T2DM
and control subjects are shown in Table 1. Patients with
T2DM had a greater waist circumference and there were more smokers compared to the control group.
There were no statistically significant differences
between patients with T2DM and controls in other
clinical characteristics [age, body mass index (BMI),
systolic and diastolic pressure]. A biochemical examination
of patients with T2DM showed statistically
significant higher levels of fasting glucose, Hb A1c,
total cholesterol, HDL, LDL, triglyceride and hsCRP
compared with the control group (Table 1). Moreover,
higher CIMT was found in patients with T2DM in
comparison with subjects without T2DM (Table 1).
The ultrasound examination of the carotid artery
was performed at the time of enrollment in the
study, and 3.8 ± 0.5 years after the initial examination.
Changes in the progression of atherosclerotic markers
(change in annual CIMT increase, change in the number
of plaque segments and change in the sum of the
plaque thickness) between subjects with T2DM and
the control group are shown in Table 2. Statistically
significantly faster progression of the atherosclerotic
markers was shown in subjects with T2DM in comparison
with the control group (Table 2).
The distribution of genotypes in the population
of patients with T2DM was in Hardy-Weinberg equilibrium
(T2DM: χ2 = 0.45; p = 0.50; control group:
χ2 = 1.46; p = 0.23). Table 3 outlines differences in
the ultrasound markers of carotid artery atherosclerosis
(initial ultrasound examination) in patients with
T2DM with regard to the rs668 genotypes. The differences
were not statistically significant with regard
to rs668 genotypes (Table 3). We did not demonstrate
statistically significant differences in the markers of
subclinical carotid atherosclerosis between different
genotypes in subjects with T2DM (Table 4).
Table 5 shows the relation between the rs668 and
the incidence of either plaques or unstable plaques in subjects with T2DM. When adjusted to other risk
factors, the rs668 GG genotype was associated with
an increased risk of carotid plaques in subjects with
T2DM (Table 5).
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