Abstract
Background
The Study of Cardiovascular Risk in Adolescents (Portuguese acronym, “ERICA”) is a multicenter, school-based country-wide cross-sectional study funded by the Brazilian Ministry of Health, which aims at estimating the prevalence of cardiovascular risk factors, including those included in the definition of the metabolic syndrome, in a random sample of adolescents aged 12 to 17 years in Brazilian cities with more than 100,000 inhabitants. Approximately 85,000 students were assessed in public and private schools. Brazil is a continental country with a heterogeneous population of 190 million living in its five main geographic regions (North, Northeast, Midwest, South and Southeast). ERICA is a pioneering study that will assess the prevalence rates of cardiovascular risk factors in Brazilian adolescents using a sample with national and regional representativeness. This paper describes the rationale, design and procedures of ERICA.
Methods/Design
Participants answered a self-administered questionnaire using an electronic device, in order to obtain information on demographic and lifestyle characteristics, including physical activity, smoking, alcohol intake, sleeping hours, common mental disorders and reproductive and oral health. Dietary intake was assessed using a 24-hour dietary recall. Anthropometric measures (weight, height and waist circumference) and blood pressure were also be measured. Blood was collected from a subsample of approximately 44,000 adolescents for measurements of fasting glucose, total cholesterol, HDL-cholesterol, LDL-cholesterol, triglycerides, glycated hemoglobin and fasting insulin.
Discussion
The study findings will be instrumental to the development of public policies aiming at the prevention of obesity, atherosclerotic diseases and diabetes in an adolescent population.
Keywords: Cardiovascular diseases, Metabolic syndrome X, Adolescent
Background
Cardiovascular diseases (CVD) are the main cause of mortality in Brazil [1] and it is well known that children/adolescents with cardiovascular risk factors have increased atherosclerosis progression rate in adulthood [2].
The prevalence of overweight and obesity is increasing worldwide, affecting all age groups [3] and these conditions in childhood are predictive of obesity in adults [4]. Obesity in children and adolescents is strongly associated with insulin resistance, dyslipidemia and type 2 diabetes [5]. In Brazil, overweight and obesity have increased in all age groups, including children and adolescents [6]. The Household Budget Survey (POF) 2008–2009 showed a striking increase in the prevalence of overweight among adolescents (10 to 19 years of age) from 1974/1975 to 2008/2009. During this period, overweight increased from 3.7% to 21.7% in males and from 7.6% to 19.4% in females [6]. In addition to obesity and dyslipidemia, studies have shown that childhood risk factors such as smoking, elevated blood pressure, low physical activity, and low consumption of fruits and vegetables are predictive of subclinical atherosclerosis, as evaluated by carotid artery intima–media thickness, and its progression in adulthood [7,8]. Besides individual’s risk factors, low socioeconomic situation and parental smoking during childhood are predictors of increased carotid intima–media thickness [9].
What follows is a description of the design and procedures of the Study of Cardiovascular Risk Factors (Portuguese acronym, ERICA).The objective is to estimate the prevalence of cardiovascular risk factors, including diabetes mellitus, obesity, hypertension, dyslipidemia, active and passive smoking, physical inactivity, unhealthy food consumption, and the association between these factors in adolescents aged 12 through 17 years who attend public and private schools in Brazilian cities with more than 100,000 inhabitants. For non-invasive procedures, 85,000 adolescents were studied; in a sub-sample of approximately 44,000 adolescents, blood was collected for measurements of glucose, lipids, and insulinemia.
ERICA is a school-based cross-sectional multi-center study. Its specific aims are (1) to describe population patterns of anthropometric parameters; (2) to describe population patterns of blood pressure (BP) levels; (3) to assess ethnic, age, sex, socioeconomic, and regional differences in CVD risk factors prevalence rates; and (4) to study the association of CVD risk factors with life style characteristics.
Methods/Design
Study sample
ERICA’s sample consists of 85,000 adolescents aged 12 to 17 years enrolled in morning or afternoon shifts of private and public schools located in the 273 Brazilian municipalities with more than 100,000 inhabitants in July, 1, 2009. Manuscript describing ERICA’s sample is in press [10].
The population frame that was sampled was stratified into 32 geographic strata formed as follows: each of the 27 federation unit capital; and five strata comprising the municipalities of each of the five macro-regions of the country. After geographic stratification, two successive selection stages were implemented: selection of schools and selection of school classes.
The schools were selected in each geographic stratum with probability proportional to size (PPS). The size measure of each school was set equal to the ratio between the number of students in its eligible classes and the distance from the State capital. This strategy aimed to concentrate the sample around the State capitals, reducing the study’s costs and facilitating the survey logistic, particularly that related to the blood drawing.
The PPS selection was performed in each geographic stratum after sorting the school records by situation (urban or rural areas) and the school governance (private or public). One thousand two hundred and fifty one schools in 124 municipalities were selected.
In the second stage, three classes in each sampled school were selected with equal probabilities during field work. Using class year as a proxy of age, only the classes of 7th, 8th and 9th years of elementary school and 1st, 2nd and 3rd year of high school were eligible for selection.
A spreadsheet was used for class selection. The spreadsheet was specific to each sampled school, with random numbers and preprogrammed formulas for class selection and for the selection of two students who had a repeat 24-hour food dietary recall for evaluation of reliability of the dietary questionnaire.
In each selected class, all students were invited to participate in an exam consisting of interviews and anthropometric and BP measurements. Because fasting was needed for blood drawing, only those students in the morning shift classes were invited for this procedure. Schools’ and parents’ permission were secured.
Sample size estimation
For the calculation of sample size, a prevalence of the metabolic syndrome in adolescents of 4% was used with a maximum absolute error of 1% and confidence level of 95%. Using these parameters, a simple random sample size would be estimated at 1,475 adolescents. Considering that the sample is clustered by school and class, a design effect of 3 was used (a previous survey with students in Rio de Janeiro indicated a design effect for body mass index of 2.87), yielding a sample size of 4,425 adolescents. As the estimates with controlled precision had to be produced for 12 domains (6 ages × two sexes) it was estimated that the overall sample size would have to be 74,340 individuals.
The sample size allocation among the 32 strata was of a power type, proportional to the square root of the survey population in each stratum, according to the 2009 Brazilian Educational Census (reviewed in 2011) [11].
Information system
ERICA’s information system consists of four data modules. The first module, ERICA Web, requires internet access and allows performance of the following tasks: (1) registration of schools and students; (2) transfer of data to and from the server; (3) ready access to data; (4) printing of the class check list; and (5) printing of the student’s and school results.
The second module is ERICA PDA (personal digital assistant). It registers the responses to the questionnaire, anthropometric and BP measurements, and the school questionnaire.
The third module is specific for entering data from the 24-hour dietary recall (24hR).
The fourth module is a set of questions about the fasting period; it is applied before blood collection.
One of the major advantages of ERICA’s information system is that all data was immediately available after data collection.
Data storage and management is centralized at Federal University of Rio de Janeiro (Portuguese acronym, UFRJ), using a cloud service. The operational system is Windows Server 2008, the dataset is Firebird 2.5, and the language C#.NET. The software used to develop the 24 hR was Visual Studio NET 2012 (web site and desktop).
Instruments and procedures
Three questionnaires were applied: one for adolescents, one for parents/care givers, and one about school characteristics.
The questionnaire for students and that about the school were partially based on instruments used in other studies on risk factors in the young in Brazil [12].
Adolescent’s questionnaire
This questionnaire was self-administered using a PDA, model LG GM750Q. Its main areas (Table 1) were socioeconomic status, adolescent work, smoking, alcohol consumption, physical activity assessment, health and medical history, sleeping hours, feeding behavior, oral health, common mental disorder, and reproductive health.
Table 1.
Questionnaire | Issue | Variable |
---|---|---|
Adolescent | Sociodemographic characteristics | Age, gender, and race/ethnicity |
Parents’ education | ||
Household assets | ||
Number of residents/room | ||
Adolescent work | Job characteristics | |
Physical activity | Type, duration, and frequency of activity [13] | |
Active/inactive [14] | ||
Feeding behavior | Eating with parents | |
Breakfast | ||
Eating at school | ||
Eating in front of TV | ||
Snacks | ||
Drinking water | ||
Eating fish | ||
Use of sweeteners | ||
Smoking | Experimentation | |
Initiation/intensity | ||
Use of flavoured cigarrets | ||
Smoking exposure | ||
Alcohol consumption | Experimentation | |
Initiation/intensity/type of beverage | ||
Reproductive health | Sexual secondary characteristics | |
Menarche | ||
Pregnancy | ||
Use of contraceptive methods | ||
Sexual maturation self-classification using Tanner’s pictures | ||
Oral health | Gum bleeding | |
Teeth brushing | ||
Dental floss use | ||
Medical health history | Hypertension | |
Diabetes mellitus | ||
Hypercholesterolemia | ||
Ashma | ||
Bodyperception | ||
Sleep | Bed time and waketime | |
Commom mental disorders | General Health Questionnaire (GHQ12) [15] | |
Parents | Adolescent mother characteristics | Age, race/ethnicity, education Occupation |
Self-reported weight and height | ||
Family medical and health history | High blood pressure | |
Ischemic heart disease | ||
Cerebral vascular disease | ||
Diabetes mellitus | ||
High cholesterol | ||
Father’s referred weight and height | ||
Adolescent birth history | Gestational age | |
Birth weight/length | ||
Breastfeeding | ||
Birth place | ||
Adolescent medical health history | Diseases | |
Hospital admissions, including emergency admissions | ||
Adolescent sleep | Sleep duration | |
School | School general characteristics | Number of students/classes |
Number of physical education teachers | ||
Extra-curricular activities (arts, sports) | ||
Physical structure | Sports court | |
Pool | ||
Auditorium | ||
Computer lab | ||
Drinkers | ||
Eating at school | School meals | |
Food sold in school | ||
Cafeteria | ||
Food advertising |
School questionnaire
The school questionnaire was filled out by a field researcher using the PDA. It contained information about school characteristics related to physical structure, availability of physical education teachers, and school meals/sale of food (Table 1).
Parents’/caregiver’s questionnaire
Parents’/care giver’s questionnaire provided information on mothers’ educational achievement, family history of cardiovascular and metabolic diseases, and circumstances related to student’s birth (birth weight, breastfeeding). A printed form was sent to the parents’/caregivers’ by the students. This is the only information source that was collected using a hard (printed) form. Data was double entered to avoid typing errors. Table 1 describes the main variables that will be assessed.
24-hour dietary recall
Dietary intake was assessed using a 24hR in a face to face interview that was performed by trained interviewers, using a specific software to register information directly in a netbook using the multiple pass method [16]. In a random subsample of two students per class, the students responded to a second 24hR in order to estimate intra-individual variability. Food and drinks consumed were recorded for all meals and snacks before the interview, with quantities and preparation methods whenever appropriate. Portion size estimation was obtained by showing photographs included in the software. The data was electronically transferred to the central database.
After conversion of the food items to grams [17], the data set will be linked to a nutritional composition table [18] in order to obtain the macro and micronutrient consumption of each adolescent.
The MSM (Multiple Source Method) program [19] will be used to calculate, by the difference between the 1st and the 2nd 24hR, a correction factor for each macro and micronutrient to be applied to all sample. The objective is to remove the intra-individual variability and to allow the estimation of usual intake. The method is applicable to nutrient and food intake including episodically consumed foods.
Anthropometric measurements
Trained researchers, according to written standardized procedures, performed the measurements.
Height, weight and circumferences
Anthropometric measurements were done with the individuals wearing light clothing and no shoes. Height [20] was measured to the nearest 1 mm using a calibrated stadiometer (portable stadiometer Alturexata®, Minas Gerais, Brazil) with millimeter resolution and height up to 213 cm. The subjects were in full standing position (in the Frankfort horizontal plane). Measurements were made in duplicate for quality control purposes. A maximum variation of 0.5 cm was allowed between the two measurements. The PDA system automatically calculated the average of the two measures for use in the analysis. If the difference exceeded 0.5 cm, the measures were deleted in the PDA display and height was measured again.
Weight [20] was measured to the nearest 50 g using a digital scale (model P150m, 200 kg of capacity and 50 g of precision, Líder®, São Paulo, Brazil).
The body mass index (BMI), defined as weight (Kg) divided by the square of height (meters), was calculated. To determine the weight categories of adolescents, the WHO (World Health Organization) reference curves [21], using the index BMI/age, according to sex, was used. The cutoff points were: malnutrition Z-score < −3; low weight Z-score ≥ −3 and < −1; normal weight Z-score ≥ −1 and ≤ 1; overweight Z-score > 1 and ≤ 2; obesity Z-score > 2.
As an additional estimate of body fat distribution, waist circumference was measured as a surrogate of central adiposity. It was measured to the nearest 1 mm using a fiber glass anthropometric tape, with millimeter resolution and length of 1.5 meters (Sanny®, São Paulo, Brazil). The individuals was at the upright position, with abdomen relaxed at the end of gentle expiration [22]. The measurement was done horizontally, at half the distance between the iliac crest and the lower costal margin. Measurements was done in duplicate for quality control purposes. A maximum variation of 1 cm between the two measurements was allowed. The PDA system automatically calculated the average of the two measures to be used in the analysis. If the difference exceeded this value, the values will be deleted in the PDA display and the waist circumference must be measured again.
Arm length was measured from the acromion (bony extremity of the shoulder girdle) to the olecranon (tip of the elbow) using an anthropometric tape. The midpoint on the dorsal (back) surface of the arm was marked with a pen. The participant was asked to relax the arm alongside the body and the measuring tape will be placed snugly around the arm at the midpoint mark, keeping the tape horizontally [20]. The tape should not indent the skin.
Blood pressure evaluation
Blood pressure measurements were based on the 4th Report on the Diagnosis, Evaluation, and Treatment of High Blood Pressure in Children and Adolescents, published in 2004 [23]. Systolic and diastolic BP and pulse were measured using the automatic oscillometric device Omron® 705-IT(Omron Healthcare, Bannockburn, IL, USA). This model has been validated for adolescents [24] and it has been chosen due to its ease of use and the minimization of observer bias or digit preference (which are the common errors associated with the auscultatory method) [25].
The adolescent were told to avoid stimulant drugs or foods, and sit quietly for 5 minutes, with his or her back supported, feet on the floor and right arm supported, and the antecubital fossa at heart level. The appropriate cuff size for the adolescent’s upper right arm was indicated when arm circumference is registered in the PDA. Three consecutive measures were taken for each individual, with an interval of three minutes between each. The 2nd and 3rdBP readings were used in order to reduce the impact of reactivity on the blood pressure (higher first reading).
The definition of hypertension in children and adolescents was based on the normative distribution of BP in healthy children. Normal BP was defined as SBP (systolic BP) and DBP (diastolic BP) that were <90th percentile for gender, age, and height. Hypertension was defined as average SBP or DBP that were ≥95th percentile for gender, age, and height. Average SBP or DBP levels that were ≥ 90th percentile but <95thpercentile were designated as “high normal” and were considered to be an indication of heightened risk for developing hypertension. This designation is consistent with the description of pre-hypertension in adults. It is now recommended that, as with adults, children and adolescents with BP levels ≥ 120/80 mmHg but <95th percentile should be considered prehypertensive [23].
Biochemical evaluation
Blood samples were collected from a subsample of approximately 44,000 students by qualified professionals in the participating schools.
This subsample was comprised by all the students studying during the morning who accepted to collect blood and who had written permission of their parents/guardians.
Participants were oriented to keep an overnight fast within12 hours before de exam. Fasting blood samples were collected for analyses of glucose, insulin, lipid profile (total cholesterol, HDL cholesterol and triglycerides), and glycated hemoglobin (HbA1c).The cutoff points that were used for these tests are shown in Table 2. The blood samples were processed and plasma and serum separated within two hours after collection and kept between 4° and 10°C while moved to the study’s single laboratory. Table 2 contains also the description of the analytical methods used for each parameter. In a subsample of 7,800 adolescents from four States, Rio de Janeiro, Rio Grande do Sul, Ceará and Federal District, serum was stored in freezers at −80°C for future analyses.
Table 2.
Exam | Method a | Cutoff points | ||
---|---|---|---|---|
Desirable | Borderline | High | ||
Colesterol (mg/dL) (mmol/l) [26] | Enzymatic kinetics | <150 | 150-169 | ≥170 |
<3.9 | 3.9-4.39 | ≥4.4 | ||
LDL-C (mg/dL) (mmol/l) [26] | Enzymatic colorimetric assay | <100 | 100-129 | ≥130 |
<2.59 | 2.59-3.34 | ≥3.36 | ||
HDL-C (mg/dL) (mmol/l) [26] | Enzymatic colorimetric assay | ≥45 | --- | --- |
≥1.16 | ||||
Triglycerides (mg/dL) (mmol/l) [26] | Enzymatic kinetics | <100 | 100-129 | ≥130 |
<1.13 | 1.13-1.46 | ≥1.47 | ||
Glucose (mg/dL) (mmol/l) [27] | Hexoquinase method | 70-99 | 100-125,9 | ≥126 |
3.89-5.5 | 5.6-6.9 | ≥7.0 | ||
Insulin (mU/L) [28] | Chemiluminescence | <15 | 15-20 | ≥20 |
Glycated hemoglobin [27] | Ion exchange chromatography | <5.7 | --- | ≥5.7 |
aBrazilian Society of Pathology; LDL-C: low density cholesterol; HDL-C: high density cholesterol.
Notification of and referral for study findings
The results of the blood tests, anthropometric measurements and BP levels were given directly to each student. In cases where abnormal biochemical, anthropometrical or BP values were identified, according to clinical cut-off points, participants were contacted and referred to health units or to their own physicians when the following results were obtained:
Undernourishment (<−3 z score).
Obesity (>2 z score).
High BP(>95th percentile).
High total cholesterol or triglycerides levels (>170 mg/dl, >130 mg/dL, respectively).
Abnormal fasting glycemia (100–125.9 mg/dL) or diabetes mellitus suspicion (≥126 mg/dL).
The adolescent was asked to have a repeated BP measurement within one year when his/her systolic or diastolic BP were ≥90th percentile but <95th or >120/80 and <95th percentile.
The adolescent was promptly referred to a health unit when his/her glucose levels were >200 mmHg or his/her BP levels were > 99th.
Quality assurance and quality control
A pretest was conducted in a public school in Rio de Janeiro in 2011. This process provided crucial and detailed insight into the understanding of all questionnaire items by the school’s students and also allowed us to analyze logistical issues related to the various stages of the field work.
A pilot study was conducted in five cities (Rio de Janeiro, Cuiabá, Feira de Santana, Botucatu, and Campinas) located in different regions of Brazil, with participation of two public and one private school in each city. Nearly 1,300 adolescents were evaluated in this pilot study pertaining to the non-invasive procedures, and for 600 students in the morning shift, blood samples were collected. The data analysis of the pilot study provided clues about points to be reinforced in the training of supervisors and field work.
To prevent or minimize errors during the data collection, procedures were adopted to ensure the quality of information. An operations manual was prepared with detailed descriptions of the standardized procedures. The field team was carefully trained before the start of the study. Data collection was monitored throughout the study.
Internal and external quality control (QC) was conducted by the study’s laboratory. Internal QC was performed daily to monitor reliability through repeated measurements of the same sample. External QC or proficiency testing was monitored accuracy through comparisons between the study’s laboratory and a gold standard laboratory. During the study, phantom samples was available from the Brazilian Society of Pathology (Control Lab) [29] and the Brazilian Society of Clinical Analysis (National Program of Quality Control) [30] for this purpose.
Training
Training of field workers was performed by the ERICA’s central coordination team according to the study protocol. Videos were especially produced for the training of anthropometric and BP measures. Interviewers were trained in anthropometric measurements using the Habicht’s criterion as a guide [31].
A series of logic checks were conducted regularly to identify outliers, discrepancies or digit preference in measurements. Appropriate measures were taken whenever problems were detected. If necessary, examiners were retrained, and equipment was constantly checked and replaced.
Extreme values were those suspected to be unusual, but permitted by the instruments. An alert rule was created so that when more than 10% of the records of an observer were above or below the 5th and 95th percentiles, according to the measurements obtained in the pilot study, a suspected measurement error was flagged, and indicated the need for retraining the observer.
Study planning and management
The study’s Steering Committee was responsible for planning, overseeing the conduct of the study and applying appropriate corrective measures based on QC results. In each of the 27 Federal (geographic) Units (26 States and the Federal District), local leaders managed the regional data collection. Several researchers collaborated as consultants at different stages of the study. Subcommittees worked to develop tools and strategies for data collection, development of the information system and QC. Members of the Steering Committee developed an operation manual and trained teams of 27 regional leaders and field supervisors. In each state, 3 to 6 teams of supervisors were trained.
A firm with extensive experience in logistics of large scale research was hired to recruit and train the field staff, under the supervision of the Steering Committee and the regional leaders. Each team had five field workers and two supervisors. The same firm was responsible for transporting the equipment between States.
Statistical analysis
When analyzing the data, the sample weights corresponding to the reciprocal of the product of the inclusion probabilities in each sample stage will be considered. A correction for non-response will be introduced in the weights. The need for sample weight calibration by sex and each age class will also be considered.
Prevalence rates, confidence intervals, and measures of central tendency will be estimated taking into account the sampling weights and the other structural sample design variables (stratum and primary sampling unit-PSU). Expected outcome measures (prevalence rates and mean variances) and differences between groups (age, gender and urban/rural groups) will be calculated with 95% confidence intervals. Sampling error, which could potentially affect the reliability and thus accuracy of the study results, will be estimated.
The association between demographic, anthropometric, metabolic and lifestyle habits will be investigated in unadjusted analysis as well as stratified and multivariate models. Statistical tests will be applied according to the data distribution and homogeneity of variances of the groups under comparison. An important focus of these analyses is the potential heterogeneity of risk relationships across regions. Testing for interaction will thus be undertaken when appropriate.
Ethical issues
This study was conducted according to the principles of the Helsinki declaration. The Ethical Committee of the Universidade Federal do Rio de Janeiro approved the study in January, 2009. The approval of the Ethical Committee at each of the 26 States and for the Federal District was obtained. Permission to conduct the study was obtained in all State and local Departments of Education and in all schools.
Written informed consent was obtained from each student, and also from their parents for those who are invited to take blood collection (those studying in the morning). When the local ethics committees require informed parental consent even for students who was not taking blood, such consent was required for students to participate in the study.
During the data collection, care was taken to guarantee the student’s privacy and confidentiality, such as when using folding screens for anthropometric measurements.
Discussion
The development of ERICA’s procedures presented many challenges. This survey was not only large from the sample size viewpoint, but it was also implemented on a huge geographic scale and in often adverse and heterogeneous conditions. Brazil is the fifth-largest country in the world, so studying a nationally representative sample presents enormous logistic challenges. For the management of a study of such magnitude, the development of an information system with maximum agility was critical.
ERICA will estimate the national prevalence of multiple cardiovascular risk factors in adolescents, including BP and biochemical parameters, not evaluated in other national studies, and will also allow the investigation of their reciprocal relationships and with other health determinants. It will, in addition, be possible to investigate interactions between several socio-demographic characteristics, including region of the country, and selected outcomes, such as diabetes mellitus and hypertension.
The storage of frozen blood in three cities will enable the investigation of inflammatory markers and other possible markers related to cardiovascular diseases and the metabolic syndrome.
Several features such as lifestyle habits, physical activity, smoking, alcohol consumption, minor psychiatric disorders and morbidity such as asthma will be assessed through a questionnaire carefully developed by experts. Details about some eating behaviors, self-perception of weight, hours spent in front of screens and reproductive health and oral hygiene will also be analyzed.
Characteristics of the infrastructure of the school, such as the existence of sports courts and number of physical education teachers, will be correlated with characteristics of adolescents and presence of cardiovascular risk factors.
Another line of research to be followed includes information obtained through the parents/care givers’ questionnaire. Information on birth weight and breastfeeding will be analyzed looking for possible associations with obesity, hypertension and altered glucose and lipid metabolism. Obtaining the name of the mother in these questionnaires will enable the use of techniques of probabilistic database linkage to relate the data from ERICA to the data on Live Births - SINASC. This linkage will allow more detailed information about relevant pregnancy characteristics and birth weight.
Participation of children and adolescents in the labor market is still a matter of debate in Brazil. ERICA will provide information for analysis of the impact of adolescent labor in the distribution of cardiovascular risk factors.
Another strength of ERICA is the possibility of developing BP, weight, height, BMI, and waist circumference distributions by sex, age and, height in Brazilian adolescents. Anthropometric measures can also be analyzed in relation to the adolescents’ self-classifications of sexual maturation, using Tanner’s criteria.
ERICA’s results will contribute to the knowledge about risk factors for atherosclerosis in a young Brazilian population, which may be used not only in guiding adolescents and parents with regard to preventive measures but also in supporting the development of effective, evidence-based health policy involving different sectors of society for the prevention and control of risk factors for diabetes and cardiovascular disease in adolescents. In addition, ERICA will facilitate partnerships between Brazilian academic institutions, as well as between the academia and health and educational public services.
Acknowledgments
We thank Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ) for providing a doctoral fellowship to GAA (process n° E26/100.332/2013). KVB (process n° 304595/2012-8), GVV (process n° 307988/2011-2), and MS (process n° 302877/2009-6) were partially supported by Conselho Nacional de Pesquisa (CNPq).
The study ERICA was supported by the Brazilian Ministry of Health (Science and Technology Department) and the Brazilian Ministry of Science and Technology (Financiadora de Estudos e Projetos/FINEP and Conselho Nacional de Pesquisa/CNPq) (grants FINEP: 01090421, CNPq: 565037/2010-2 and 405009/2012-7).
Abbreviations
- 24hR
24-hour dietary recall
- BMI
Body mass index
- BP
Blood pressure
- CVD
Cardiovascular diseases
- DBP
Diastolic blood pressure
- ERICA
Estudo de Riscos Cardiovasculares em Adolescentes (Study of Cardiovascular Risk Factors)
- MSM
Multiple Source Method
- PDA
Personal digital assistant
- POF
Pesquisa de Orçamentos Familiares (Household Budget Survey)
- PPS
Proportional to size
- QC
Quality control
- SBP
Systolic blood pressure
- UFRJ
Universidade Federal do Rio de Janeiro (Federal University of Rio de Janeiro)
- WHO
World Health Organization
Footnotes
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
KVB, MS, MCCK, CHK, MTLV, GAA, LAB, GVV and VCF have made substantial contributions to the conception and design of the study, drafted the manuscript and revised it critically. AD, AJPM, ALLS, AMAO, BDS, CLO, CFC, DTG, DRB, DLBR, ELS, EBL, EF, ERAO, FAGV, GDA, GSB, GMD, HRCF, MIM, ICBG, JRFN, JSO, KMBC, LGOG, MMS, PTM, PCBVJ, PAMF, RMMJr, RQG, RPV, SMV, SSM, SMSM, TBLG, BMT, ESM and TLNS contributed to the conception and design of the study, and revised the manuscript. All authors read and approved the final manuscript.
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Pedro Antônio Muniz Ferreira, Email: pedroamf@terra.com.br.
Renan Magalhães Montenegro, Jr, Email: renanmmjr@gmail.com.
Ricardo Queiroz Gurgel, Email: ricardoqgurgel@gmail.com.
Rodrigo Pinheiro Vianna, Email: vianna@ccs.ufpb.br.
Sandra Mary Vasconcelos, Email: sandra-mary@hotmail.com.
Sandro Silva da Matta, Email: profsandrodamatta@terra.com.br.
Stella Maris Seixas Martins, Email: stellamsmartins@hotmail.com.
Tamara Beres Lederer Goldberg, Email: tamara@fmb.unesp.br.
Thiago Luiz Nogueira da Silva, Email: thiagolns@gmail.com.
References
- 1.Schmidt MI, Duncan BB, Silva GA, Menezes AM, Monteiro CA, Barreto SM, et al. Chronic non-communicable diseases in Brazil: burden and current challenges. Lancet. 2011;377(9781):1949–1961. doi: 10.1016/S0140-6736(11)60135-9. [DOI] [PubMed] [Google Scholar]
- 2.Juonala M, Viikari JS, Kahonen M, Taittonen L, Laitinen T, Hutri-Kahonen N, et al. Life-time risk factors and progression of carotid atherosclerosis in young adults: the Cardiovascular Risk in Young Finns study. Eur Heart J. 2010;31(14):1745–1751. doi: 10.1093/eurheartj/ehq141. [DOI] [PubMed] [Google Scholar]
- 3.WHO. Obesity – preventing and managing the global epidemic. Geneva: Report of a WHO Consultation on Obesity. In: World Health Organization; 2004. [PubMed]
- 4.Juonala M, Magnussen CG, Berenson GS, Venn A, Burns TL, Sabin MA, et al. Childhood adiposity, adult adiposity, and cardiovascular risk factors. N Engl J Med. 2011;365(20):1876–1885. doi: 10.1056/NEJMoa1010112. [DOI] [PubMed] [Google Scholar]
- 5.Williams DE, Cadwell BL, Cheng YJ, Cowie CC, Gregg EW, Geiss LS, et al. Prevalence of impaired fasting glucose and its relationship with cardiovascular disease risk factors in US adolescents, 1999–2000. Pediatrics. 2005;116(5):1122–1126. doi: 10.1542/peds.2004-2001. [DOI] [PubMed] [Google Scholar]
- 6.IBGE. Pesquisa de Orçamentos Familiares (POF). Antropometria e estado nutricional de crianças, adolescentes e adultos no Brasil; 2008–2009. Rio de Janeiro: Instituto Brasileiro de Geografia e Estatística; 2010; 130.
- 7.Freedman DS, Khan LK, Dietz WH, Srinivasan SR, Berenson GS. Relationship of childhood obesity to coronary heart disease risk factors in adulthood: the Bogalusa Heart Study. Pediatrics. 2001;108(3):712–718. doi: 10.1542/peds.108.3.712. [DOI] [PubMed] [Google Scholar]
- 8.Franks PW, Hanson RL, Knowler WC, Sievers ML, Bennett PH, Looker HC. Childhood obesity, other cardiovascular risk factors, and premature death. N Engl J Med. 2010;362(6):485–493. doi: 10.1056/NEJMoa0904130. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Juonala M, Viikari JS, Raitakari OT. Main findings from the prospective cardiovascular risk in young Finns study. Curr Opin Lipidol. 2013;24(1):57–64. doi: 10.1097/MOL.0b013e32835a7ed4. [DOI] [PubMed] [Google Scholar]
- 10.Vasconcellos MTL, Silva PLN, Szklo M, Bloch KV, Kuschnir MCC, Klein CH, et al. Desenho da amostra do Estudo de Riscos Cardiovasculares em Adolescentes (ERICA). Cadernos de Saúde Pública. 2015; In press.
- 11.Censo Escolar - Inep. [http://portal.inep.gov.br/basica-censo]
- 12.Castro IR, Cardoso LO, Engstrom EM, Levy RB, Monteiro CA. Surveillance of risk factors for non-communicable diseases among adolescents: the experience in Rio de Janeiro, Brazil. Cad Saude Publica. 2008;24(10):2279–2288. doi: 10.1590/S0102-311X2008001000009. [DOI] [PubMed] [Google Scholar]
- 13.Farias Junior JC, Lopes AS, Mota J, Santos MP, Ribeiro JC, Hallal PC. Validade e reprodutibilidade de um questionário para medida de atividade física em adolescentes: uma adaptação do Self-Administered Physical Activity Checklist. Rev bras epidemiol. 2012;15(1):198-210. [DOI] [PubMed]
- 14.Biddle S, Sallis JF, Cavill NA. Young and active? Young people and health enhancing physical activity. Evidence and implication. London: Health Education Authority; 1998. [Google Scholar]
- 15.Mari JJ, Williams P. A comparison of the validity of two psychiatric screening questionnaires (GHQ-12) Psychol Med. 1985;15(3):651–659. doi: 10.1017/S0033291700031500. [DOI] [PubMed] [Google Scholar]
- 16.Conway JM, Ingwersen LA, Vinyard BT, Moshfegh AJ. Effectiveness of the US Department of Agriculture 5-step multiple-pass method in assessing food intake in obese and nonobese women. Am J Clin Nutr. 2003;77(5):1171–1178. doi: 10.1093/ajcn/77.5.1171. [DOI] [PubMed] [Google Scholar]
- 17.IBGE . Pesquisa de Orçamentos Familiares (POF), 2008–2009. Tabela de medidas referidas para os alimentos consumidos no Brasil. Rio de Janeiro: Instituto Brasileiro de Geografia e Estatística; 2011. [Google Scholar]
- 18.IBGE . Pesquisa de Orçamentos Familiares (POF), 2008–2009. Tabela de composição nutricional dos alimentos consumidos no Brasil. Rio de Janeiro: Instituto Brasileiro de Geografia e Estatística; 2011. [Google Scholar]
- 19.Multiple Source Method (MSM). [https://msm.dife.de/]
- 20.Lohman TG, Roche AF, Martorell R. Anthropometric standardization reference manual: Human Kinetics Books; 1988.
- 21.de Onis M, Onyango AW, Borghi E, Siyam A, Nishida C, Siekmann J. Development of a WHO growth reference for school-aged children and adolescents. Bull World Health Organ. 2007;85(9):660–667. doi: 10.2471/BLT.07.043497. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.WHO Obesity: preventing and managing the global epidemic. Report of a WHO consultation. World Health Organ Tech Rep Ser. 2000;894:i–xi. [PubMed] [Google Scholar]
- 23.National High Blood Pressure Education Program Working Group on High Blood Pressure in Children The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents. Pediatrics. 2004;114(2 Suppl 4th Report):555–576. [PubMed] [Google Scholar]
- 24.Stergiou GS, Yiannes NG, Rarra VC. Validation of the Omron 705 IT oscillometric device for home blood pressure measurement in children and adolescents: the Arsakion School Study. Blood Press Monit. 2006;11(4):229–234. doi: 10.1097/01.mbp.0000209074.38331.16. [DOI] [PubMed] [Google Scholar]
- 25.Pickering TG, Hall JE, Appel LJ, Falkner BE, Graves J, Hill MN, et al. Recommendations for blood pressure measurement in humans and experimental animals: part 1: blood pressure measurement in humans: a statement for professionals from the Subcommittee of Professional and Public Education of the American Heart Association Council on High Blood Pressure Research. Circulation. 2005;111(5):697–716. doi: 10.1161/01.CIR.0000154900.76284.F6. [DOI] [PubMed] [Google Scholar]
- 26.Xavier HT, Izar MC, Faria Neto JR, Assad MH, Rocha VZ, Sposito AC, et al. V Brazilian Guidelines on Dyslipidemias and Prevention of Atherosclerosis. Arq Bras Cardiol. 2013;101(4 Suppl 1):1–20. doi: 10.5935/abc.2013S010. [DOI] [PubMed] [Google Scholar]
- 27.Diagnosis and Classification of Diabetes Mellitus. Diabetes Care. 2010; 33(Supplement 1):S62-S69. [DOI] [PMC free article] [PubMed]
- 28.Back Giuliano Ide C, Caramelli B, Pellanda L, Duncan B, Mattos S, Fonseca FH: I Guidelines of Prevention of Atherosclerosis in Childhood and Adolescence. Arq Bras Cardiol. 2005; 85 Suppl 6:4–36. [PubMed]
- 29.Sociedade Brasileira de Patologia Clínica. Medicina Laboratorial. [http://www.sbpc.org.br/?C=133]
- 30.American Diabetes Association. Programa Nacional de Controle de Qualidade. [http://www.pncq.org.br/]
- 31.Habicht JP. Standardization of quantitative epidemiological methods in the field. Bol Oficina Sanit Panam. 1974;76(5):375–384. [PubMed] [Google Scholar]