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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 26, No 1, January/February 2015

AFRICA

21

Circulating adhesion molecules and arterial stiffness

Ismail Dogu Kilic, Gulin Findikoglu, Yusuf I Alihanoglu, Bekir Serhat Yildiz, Sukriye Uslu, Simin Rota,

Harun Evrengul

Abstract

Aim:

VCAM-1 and ICAM-1 are two important members of

the immunoglobulin gene superfamily of adhesion molecules,

and their potential role as biomarkers of diagnosis, severity

and prognosis of cardiovascular disease has been investigated

in a number of clinical studies. The aim of the present study

was to determine the relationship between circulating ICAM-

1 and VCAM-1 levels and aortic stiffness in patients referred

for echocardiographic examination.

Methods:

Aortic distensibility was determined by echocar-

diography using systolic and diastolic aortic diameters in 63

consecutive patients referred for echocardiography. Venous

samples were collected in the morning after a 12-hour over-

night fast, and serumconcentrations of ICAM-1 andVCAM-1

were measured using commercial enzyme immunoassay kits.

Results:

Data of a total of 63 participants (mean age 55.6

±

10.5 years, 31 male) were included in the study. Circulating

levels of adhesion molecules were VCAM-1: 12.604

±

3.904

ng/ml and ICAM-1: 45.417

±

31.429 ng/ml. We were unable

to demonstrate any correlation between indices of aortic stiff-

ness and VCAM-1 and ICAM-1 levels.

Conclusion:

The role of soluble adhesion molecules in cardio-

vascular disease has not been fully established and clinical

studies show inconsistent results. Our results indicate that

levels of circulating adhesion molecules cannot be used as

markers of aortic stiffness in patients.

Keywords:

VCAM-1, ICAM-1, adhesion molecules, aortic stiff-

ness

Submitted 14/7/14, accepted 18/9/14

Cardiovasc J Afr

2015;

26

: 21–24

www.cvja.co.za

DOI: 10.5830/CVJA-2014-060

Damage to or stimulation of the endothelium leads

to the increased expression and release of molecules that

trigger leukocyte homing, adhesion and migration into the

subendothelial space, which are fundamental stages of the

development and progression of atherosclerosis.

1

Among these,

adhesion molecules play a key role. Adhesion molecules are

substances that mediate the interaction between cells, their

extracellular matrices and endothelial surfaces. They function as

receptors that trigger intracellular pathways and participate in

the control of vital processes.

2

Once expressed on the endothelial surface, soluble forms of

adhesion molecules may be found in the circulation, released

either via shedding or proteolytic cleavage, and are considered

markers of increased expression of membrane-bound adhesion

molecules.

3-5

Vascular cell adhesion molecule 1 (VCAM-1) and

intercellular adhesion molecule 1 (ICAM-1) are two important

members of the immunoglobulin gene superfamily of adhesion

molecules and their potential role as biomarkers of diagnosis,

severity and prognosis of cardiovascular disease has been

investigated in a number of clinical studies.

6

Decreased arterial compliance is one of the earliest signs

of adverse structural and functional changes within the vessel

wall.

7

Increased arterial stiffness represents a physiological

aspect of ageing, however, this process can be accelerated

by cardiovascular risk factors, and has been shown to be an

independent predictor of cardiovascular morbidity and all-cause

mortality in various populations.

8-10

Although studies have also demonstrated that increased

arterial stiffness is associated with inflammation, data on the

association between aortic distensibility and soluble adhesion

molecules are sparse.

11

The purpose of the present study was

to determine the relationship between circulating ICAM-1 and

VCAM-1 levels as inflammatory markers, and aortic stiffness in

patients referred for echocardiographic examination.

Methods

Sixty-three consecutive patients who were referred for

echocardiography were included in the study. Patients with renal

or hepatic failure, known infectious or inflammatory disease,

acute illness, moderate-to-severe valvular dysfunction, aortic

dissection or other aortic disease, or poor acoustic quality were

excluded. The study was approved by our local ethics committee,

and written informed consent was obtained from each participant.

Aortic stiffness measurements were performed on the subjects

in the left lateral decubitus position with echocardiography,

using a Vivid 7 Doppler echocardiographic unit (GE Vingmed

Ultrasound, Horten, Norway) with a 2.5-MHz probe. The aortic

diameter was recorded by M-mode echocardiography at a level

of 3 cm above the aortic valve.

Internal aortic diameters were measured by means of a caliper

in systole and diastole as the distance between the trailing edge

of the anterior aortic wall and the leading edge of the posterior

Department of Cardiology, Medical Faculty, Pamukkale

University, Denizli, Turkey

Ismail Dogu Kilic, MD,

idogukilic@gmail.com

Yusuf I Alihanoglu, MD

Bekir Serhat Yildiz, MD

Harun Evrengul, MD

Department of Physical Medicine and Rehabilitation,

Cardiopulmonary Unit, Medical Faculty, Pamukkale

University, Denizli, Turkey

Gulin Findikoglu, MD

Finike State Hospital, Antalya, Turkey

Sukriye Uslu, MD

Department of Biochemisty, Medical Faculty, Pamukkale

University, Denizli, Turkey

Simin Rota, MD