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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 26, No 3, May/June 2015

AFRICA

115

mechanical function have recently been identified as a potential

indicator of cardiac disease and arrhythmias.

14,15

Prolongation of

atrial electromechanical interval and impaired LA mechanical

function are associated with adverse clinical events, including

atrial fibrillation, stroke, diastolic dysfunction and left ventricular

failure.

16,17

LA mechanical function and atrial conduction abnormalities

have not been investigated in MP users and smokers. Therefore,

our study was planned to evaluate whether MP damages

intra- and inter-atrial conduction intervals and LA mechanical

function as much as cigarette smoking.

Methods

A total of 150 chronic MP users (50 males, mean age 32.5

±

5.4

years), cigarette smokers (50 males, mean age 32.1

±

6.0 years)

and controls (50 males, mean age 30.1

±

5.8 years) who referred

to various out-patient departments (cardiology clinic, public

health clinic, internal medicine clinic, cardiovascular surgery

clinic) and were matched for age and gender, were included in

the study. A medical history was taken and detailed physical

examinations were performed on all subjects.

The inclusion criterion was using MP for at least three years.

A package of MP was considered sufficient to provide use of the

powder for 20 occasions. Duration and frequency of MP use,

duration of cigarette smoking and number of cigarettes smoked

throughout the day were recorded. The entire study population’s

demographic characteristics, biochemical parameters, lipid

values and ECGs were obtained.

Exclusion criteria were: history of coronary artery disease,

arterial hypertension, hypercholesterolaemia, diabetes mellitus,

primary cardiomyopathy, valvular heart disease, left ventricular

ejection fraction (LVEF) less than 50%, bundle branch block,

LV wall motion abnormality, renal failure, atrioventricular

conduction abnormalities on electrocardiogram, thyroid

dysfunction, anaemia, electrolyte imbalance, pulmonary disease,

and poor-quality echocardiographic and electrocardiographic

imaging.

All patients were in sinus rhythm, and none was taking

medication such as anti-arrhythmics, antihistamines, tricyclic

antidepressants and antipsychotics. Written informed consent

was obtained from each subject. The institutional ethics

committee approved the study protocol.

Echocardiography

In this study, a Vingmed Vivid Seven Pro, Doppler

echocardiographic (GE Ultrasound, Horten, Norway) unit

with a 2–4 MHz FPA probe was used. Tissue Doppler (TDI)

echocardiography was performed with a transducer frequency of

3.5–4.0 MHz, adjusting the spectral pulsed Doppler signal filters

to obtain the Nyquist limit of 15–20 cm/s, and using the minimal

optimal gain setting. The monitor sweep speed was set at 50–100

mm/s to optimise the spectral display of myocardial velocities.

A 12-lead electrocardiogram recording obtained from the

same derivation (DII derivation) was recorded continuously

during the echocardiographic examination in all study

subjects. Two-dimensional, M-mode, pulsed and colour-flow

Doppler echocardiographic examinations were performed by a

cardiologist who was blinded to the clinical details and findings

of other examinations of each subject and control. During

echocardiography, continuous one-lead electrocardiographic

recordings were obtained. LA volumetric parameters were

measured by transthoracic echocardiography in the left lateral

position, in parasternal long axis, apical four chambers and two

chambers. M-mode measurements and conventional Doppler

echocardiographic examinations were performed according to

the guidelines of the American Society of Echocardiography.

18

All measurements were recorded as averages of three cardiac

cycles. LA dimension, LV end-systolic and end-diastolic

dimensions, diastolic ventricular septal thickness, and diastolic

LV posterior wall thickness were measured in the parasternal

long-axis view. LVEF was estimated using the Simpson’s rule.

All echocardiographic examinations were performed by the same

cardiologist.

LA volumes were measured echocardiographically using

the biplane area–length method in apical four-chamber and

two-chamber views. LA maximal volume (V

max

) was recorded

at the onset of mitral opening, LA minimal volume (V

min

) was

recorded at the onset of mitral closure, and LA pre-systolic

volume (V

p

) was recorded at the beginning of the atrial systole

(P wave on ECG). All volume measurements were corrected to

body surface area, expressed as ml/m

2

and the following LA

emptying function parameters were calculated:

19

LA passive emptying volume (LAPEV)

=

V

max

– V

p

LA passive emptying fraction (LAPEF)

=

​ 

LAPEV

_______

V

max

LA active emptying volume (LAAEV)

=

V

p

– V

min

LA active emptying fraction (LAAEF)

=

​ 

LAAEV

_______

V

p

LA total emptying volume (LATEV)

=

V

max

– V

min

LA total emptying fraction (LATEF)

=

​ 

LATEV

_______

V

max

All measurements were repeated during three consecutive heart

beats and the average of three consecutive measurements was

obtained.

Atrial electromechanical coupling measurements

For atrial electromechanical intervals in the apical four-chamber

view, the pulsed Doppler sample volume was placed at the level

of the LV lateral mitral annulus, septal mitral annulus and right

ventricular (RV) tricuspid annulus. Atrial electromechanical

intervals (PA) were measured as the time interval between the

onset of the P wave on the electrocardiogram and the beginning

of the late diastolic A wave at the lateral mitral annulus (lateral

PA), septal mitral annulus (septal PA), and RV tricuspid annulus

(RV PA). The difference between lateral PA and RV PA (lateral

PA–RV PA) was defined as inter-atrial dyssynchrony, and the

difference between septal PA and RV PA (septal PA–RV PA) as

intra-atrial dyssynchrony.

20

Reproducibility

Intra-observer variability was assessed in 20 subjects selected

randomly from the study groups by repeating the measurements