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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 31, No 3, May/June 2020

148

AFRICA

apoptosis and phagocytosis, as well as in pathological processes

such as inflammation, fibrosis and atherosclerosis.

10-13

It has

been suggested that it plays a key role in atherogenesis through

increased phagocytosis and induction of the proliferation of

vascular smooth muscle cells (VSMCs).

14,15

In addition, Gal-3 has been shown to play a central

pathophysiological role in the development of cardiovascular

diseases by enhancing cardiac hypertrophy, fibrosis, arterial

stiffness, inflammation and oxidative stress during cardiovascular

remodelling.

8

Recent studies have demonstrated not only the

potential role of Gal-3 in atherogenesis, but also an association

between increased Gal-3 expression and the development of

atherogenesis.

15

In the literature, there are several studies carried out in

animal and human models. In an animal model, inhibition of

Gal-3 was found to be associated with decreased atherosclerotic

plaque volume in mice with apolipoprotein E deficiency.

16

In a

recent study, the utility of Gal-3 as a diagnostic and prognostic

marker for cardiovascular conditions was reported.

17

In the light

of these data, Gal-3, which is associated with inflammation and

atherosclerosis, may play a major role in coronary artery disease

(CAD) as well as in CAE, which is considered to represent a

variant of CAD and to have a similar aetiopathology and clinical

course.

18

To the best of our knowledge, there is no study in the

literature examining serum Gal-3 levels in patients with isolated

CAE. In this study therefore we aimed to investigate the possible

relationship between serum Gal-3 levels and isolated CAE.

Methods

In this prospective, case-controlled study, we included a total of

49 consecutive isolated CAE patients diagnosed with CAE by

coronary angiography at the catheter laboratory of Medeniyet

University, Goztepe Training and Research Hospital between

March 2016 and March 2017. The control group consisted

of a total of 43 individuals with normal coronary arteries.

Detailed demographic data were obtained from each patient.

Physical examination, medical history, blood biochemistry and

transthoracic echocardiography were performed in both groups

to rule out systemic conditions.

Hypertension was defined as a systolic blood pressure of ≥

140 mmHg and/or a diastolic blood pressure of ≥ 90 mmHg

or current use of hypertensive agents. Diabetes was defined as

fasting blood glucose of > 126 mg/dl (6.99 mmol/l) or current

use of a diet or oral antidiabetic agents to lower blood glucose

levels. The use of anti-hyperlipidaemic agents or a fasting plasma

total cholesterol of > 200 mg/dl (5.18 mmol/l) or a low-density

lipoprotein cholesterol (LDL-C) of > 130 mg/dl (3.37 mmol/l)

were considered to denote hyperlipidaemia.

Exclusion criteria were as follows: the presence of acute

coronary syndrome, left ventricular dysfunction (ejection

fraction < 50%), left ventricular hypertrophy, valvular heart

disease, peripheral vascular disease, congenital cardiac disease,

hepatic, renal, inflammatory or connective tissue, infectious or

autoimmune disorders and malignancy.

A written informed consent was obtained from each

participant. The study protocol was approved by the local ethics

committee. The study was conducted in accordance with the

principles of the Declaration of Helsinki.

Morning venous blood samples were obtained after 12

hours of fasting. Serum glucose, creatinine, high-sensitivity

C-reactive protein (hs-CRP), total cholesterol, LDL-C, high-

density lipoprotein cholesterol (HDL-C) and triglycerides were

measured using standard laboratory methods. Additional blood

sampling was performed to measure serumGal-3 concentrations.

Blood samples were immediately centrifuged at 1 000 μg for 15

minutes and sera were separated and stored at –80°C until Gal-3

assays. Serum Gal-3 concentrations were analysed in a blinded

manner using a commercial enzyme-linked immunosorbent assay

(ELISA) in accordance with the manufacturer’s instructions

(eBioscience, CA, USA). The values were normalised to the

standard curve. Intra-assay and inter-assay variance for Gal-3

at a Gal-3 concentration of 1.5 ng/ml were 6.4 and 11.4%,

respectively.

Indications for coronary angiography were the presence of

typical angina pectoris symptoms or suspicious or positive test

results in non-invasive methods to assess coronary ischaemia

(dobutamine stress echocardiography, treadmill test ormyocardial

perfusion scintigraphy). Coronary angiography was performed

using the Judkins technique with left heart catheterisation and

without the use of nitroglycerine (Siemens, Medical Solutions

2007, Munich, Germany). The angiography results were based

on agreement between two experienced angiography specialists

blinded to the study groups. Isolated CAE was defined as the

dilatation of coronary arteries with a diameter of 1.5 times or

greater than that of the adjacent normal coronary artery without

significant stenotic lesions.

1,2

In the absence of an identifiable adjacent normal segment,

the mean diameter of the corresponding coronary segment in

the control group was accepted as the normal value. The severity

of ectasia was defined according to the Markis classification

on the basis of the extent of ectatic involvement, as follows,

in decreasing order of severity: diffuse ectasia in two or three

vessels (type 1); diffuse involvement in one vessel and segmental

involvement in another vessel (type 2); diffuse involvement in a

single vessel (type 3); and segmental or localised involvement

(type 4).

7

Statistical analysis

Statistical analysis was performed using the Statistical Package

for the Social Sciences (SPSS) version 22.0 software (IBM

Corp, Armonk, NY, USA). Descriptive data are expressed as

mean ± standard deviation (SD), median (min–max) or number

and frequency. The distribution of variables was analysed

using the Kolmogorov–Smirnov test. The Mann–Whitney

U

-test

and independent samples

t

-test were used for the analysis of

quantitative data. The chi-squared test was used for analysis

of qualitative data, and Fisher’s exact test was used when the

chi-squared test was not suitable. The impact level and cut-off

values were assessed using receiver operating characteristic

(ROC) curves. The impact level was examined using univariate

and multivariate logistic regression analyses. A

p-

value of < 0.05

was considered statistically significant.

Results

In the study population there were 31 males and 18 females in the

isolated CAE group and 19 males and 24 females in the control