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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 27, No 5, September/October 2016

316

AFRICA

primary education in a public school in Luanda, the Angolan

capital. The project was carried out after obtaining authorisation

from the Provincial Directorate of Education, the Education

Chamber of Rangel municipality and the directors of the school

5008 (Our Lady of Light).

Consent for the involvement of the community in the study

was obtained in meetings with the school staff, parents and/

or guardians of the children and the children to clarify the

study purposes and methods. The project was approved by the

Independent Ethics Committee on Research of the Faculty

of Medicine of Agostinho Neto University, following the

standards procedures in human research in accordance with the

Declaration of Helsinki.

In the 2011 academic year, 1 015 students (aged five to 12

years) were enrolled in the Our Lady of Light school and 719

(70.8%) were eligible for the study (seven to 11 years). This school

was chosen because it is near the Faculty of Medicine, where

data were collected and because it is located in a neighborhood

with most of the families belonging to the middle class.

After meeting with parents or guardians, we sent an

envelope containing an invitation letter and a questionnaire

to a random subsample of 290 students. The questionnaire

required completion for information on the conditions of birth

and the child’s life, including pregnancy history, birth weight,

period of exclusive breastfeeding, self-reported diseases, and

sociodemographic information of the family. Information about

birth weight and the duration of exclusive breastfeeding in

addition to signing of the consent form were necessary for final

inclusion in the project.

Of the 290 questionnaires distributed, 248 (85.5%) were

returned. Eleven children were excluded due to lack of essential

information. Of the 237 selected, 23 did not appear at the venue

for the examination. The set of examinations to investigate the

presence of cardiovascular risk factors was performed on 214

children.

All children were classified according to the Tanner scale,

20

obtained by self-evaluation of genitalia and breast development.

According to this procedure, 16 children were excluded from our

analysis because they were in Tanner stage II, or because they

had completed 12 years between enrolment and the examination.

Therefore, the data in this study refer to 198 pre-pubertal

(Tanner stage I) and apparently healthy schoolchildren.

All study participants presented to the Laboratory of

Functional Tests and Physiology of the Faculty of Medicine on

a pre-scheduled morning in a fasting condition (10–14 hours).

Examinations were performed from June 2012 to November

2013. A previous pilot study (March 2012) was performed

on 30 children (not included in this study) to standardise the

protocol and to train examiners. Sociodemographic data (age,

gender, race, school grade), physical activity and dietary habits

were obtained in an interview with the child and the mother or

guardian.

Blood was collected by venipuncture of the forearm and

processed on the same day by the Department of Biochemistry

(Faculty of Medicine) to determine glucose, urea, uric acid,

creatinine, total cholesterol, high-density lipoprotein (HDL)

cholesterol and triglyceride levels. Only reagents of BioSystems

SA (Barcelona, Spain) were used. Low-density lipoprotein (LDL)

cholesterol concentration was calculated by the Friedewald

formula for triglycerides

<

400 mg/dl (4.52 mmol/l).

Biochemical variables in the blood were classified according to

the criteria established by the American Academy of Pediatrics

and the American Heart Association (American Guidelines for

Cardiovascular Health and Risk Reduction in Children and

Adolescents 2012).

21

In brief, the lipid profile was classified as

follows:

total cholesterol

<

170 mg/d (

<

4.4 mmol/l): acceptable;

170–199 mg/dl (5.15 mmol/l): borderline;

200 mg/dl (

5.18

mmol/l): high

LDL cholesterol

<

110 mg/dl (

<

2.85 mmol/l): acceptable;

110–129 mg/dl (2.85–3.34 mmol/l): borderline; and

130 mg/

dl (

3.37 mmol/l): high

triglycerides (0–9 years)

<

75 mg/dl (

<

0.85 mmol/l): accept-

able; 75–99 mg/dl (0.85–1.12 mmol/l): borderline;

100 mg/dl

(

1.13 mmol/l): high

triglycerides (10–19 years)

<

90 mg/dl (

<

1.02 mmol/l): accept-

able; 90–129 mg/dl (1.02–1.46 mmol/l): borderline; and

130

mg/dl (

1.47 mmol/l): high

HDL cholesterol

>

45 mg/dl (

>

1.17 mmol/l): acceptable;

40–45 mg/dl (1.04–1.17 mmol/l): borderline; and

<

40 mg/dl

(

<

1.04 mmol/l): low.

21

According to fasting blood glucose criteria, the children were

classified as normoglycaemic (60–99 mg/dl) (3.33–5.49 mmol/l),

glucose intolerant (100–125 mg/dl) (5.55–6.94 mmol/l) or

hyperglycaemic (

>

125 mg/dl) (

>

6.94 mmol/l). No child was on

treatment with insulin or oral hypoglycaemic agents.

Body weight was obtained using a digital electronic scale

(SECA, Mod 763, Germany) with 0.1-kg precision while

fasting and after voiding. Children were barefoot and clothed

with undergarments only. Height was measured using a fixed

stadiometer with 0.5-cm precision. The child was placed on the

central part of the scale platform with heels together, head and

buttocks resting against the stadiometer and eyes looking toward

the Frankfurt horizontal plane.

The body mass index (BMI) was calculated by dividing body

weight by height squared (kg/m

2

). Percentiles (P) of height, weight

and BMI of each child were calculated as presented in https://

www.bcm.edu/bodycomplab/. 2

2

BMI classification was obtained

according to the following World Health Organisation (WHO)

parameters: underweight (BMI

<

P5), normal (BMI

P5 and

<

P85), overweight (BMI

P85 and

<

P95) and obese (BMI

P95).

23

The left arm circumference was obtained with an inelastic tape

at the midpoint between the acromion (proximal) and olecranon

process (distal). The waist (WC) and hip circumferences (HC)

were measured with an inelastic tape with the child in a standing

position and at the end-expiration phase. Measurements (0.1-

mm precision) were obtained in front of a mirror to facilitate the

tape positioning in the horizontal plane. WC was measured at the

midpoint between the lower edge of the rib cage and the anterior

superior iliac crest. HC was measured at the level of the great

trochanter, circling the hip on the most prominent point between

the waist and the thigh. The waist-to-hip ratio (WHR) was

obtained by dividing WC by HC. The thickness of four skinfolds

(triceps, supra-iliac, subscapular and abdominal) was measured

with a manual caliper (Sanny) with a precision of 1 mm.

Body composition was obtained by tetrapolar bio-impedance

with the Maltron BioScan Analyser (Model 916, Maltron Int

Ltd, UK). Two electrodes were placed on the dorsal surface of

the radiocarpal joint and metacarpal of the right hand and the

other two on the dorsal surface of the right foot (tibiotarsal