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Cohort Profile
 Cohort profile: the Ewha Birth and Growth Study
Hye Ah Lee1orcid, Bohyun Park2orcid, Jungwon Min3orcid, Eun Jeong Choi4orcid, Ui Jeong Kim4,5orcid, Hyun Jin Park4,5orcid, Eun Ae Park6orcid, Su Jin Cho6orcid, Hae Soon Kim6orcid, Hwayoung Lee7orcid, Young Ju Kim5,8orcid, Young Sun Hong9orcid, Eui-Jung Kim10orcid, Eun Hee Ha5,11orcid, Hyesook Park4,5orcid
Epidemiol Health 2021;43:e2021016.
DOI: https://doi.org/10.4178/epih.e2021016
Published online: February 22, 2021

1Clinical Trial Center, Ewha Womans University Mokdong Hospital, Seoul, Korea

2National Cancer Control Institute, National Cancer Center, Goyang, Korea

3Department of Biomedical and Health Informatics, Children’s Hospital of Philadelphia, Philadelphia, PA, USA

4Department of Preventive Medicine, Ewha Womans University College of Medicine, Seoul, Korea

5Graduate Program in System Health Science and Engineering, Ewha Womans University, Seoul, Korea

6Department of Pediatrics, Ewha Womans University College of Medicine, Seoul, Korea

7Department of Anatomy, Ewha Womans University College of Medicine, Seoul, Korea

8Department of Obstetrics and Gynecology, Ewha Womans University College of Medicine, Seoul, Korea

9Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea

10Department of Psychiatry, Ewha Womans University College of Medicine, Seoul, Korea

11Department of Occupational and Environmental Medicine, Ewha Womans University College of Medicine, Seoul, Korea

Correspondence: Hyesook Park Department of Preventive Medicine, Ewha Womans University College of Medicine, 25 Magokdong-ro 2-gil, Gangseo-gu, Seoul 07804, Korea E-mail: hpark@ewha.ac.kr
• Received: December 21, 2020   • Accepted: February 20, 2021

©2021, Korean Society of Epidemiology

This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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  • With the introduction of life-course epidemiology, researchers realized the importance of identifying risk factors in early life to prevent chronic diseases. This led to the establishment of the Ewha Birth and Growth Study in 2001; the study is a prospective birth cohort designed to provide evidence of early life risk factors for a child’s growth and health. Participants were recruited from those who visited Ewha Womans University Mokdong Hospital (a tertiary hospital in southwest Seoul, Korea) for prenatal care at 24-28 weeks of gestation. In total, 891 mothers enrolled in this study between 2001 and 2006 and their offspring (n=940) were followed-up. Regular check-up examinations of offspring were conducted at 3 years, 5 years, and 7 years of age and every year thereafter. To consider age-related health issues, extensive data were collected using questionnaires and measurements. In 2021, the study subjects will reach 19 years of age, and we are planning a check-up examination for early adulthood. About 20 years have passed since the cohort data were collected, and we have published results on childhood health outcomes associated with prenatal and birth characteristics, genetic and epigenetic characteristics related to childhood metabolism, the effects of exposure to endocrine disruptors, and dietary patterns in childhood. Recently, we started reporting on topics related to adolescent health. The findings will facilitate identification of early life risk factors for chronic diseases and the development of interventions for diseases later in life.
  • Keywords: Cohort studies, Child health, Cardiometabolic risk factors, Metabolic syndrome
According to a report from the World Health Organization, 41 million people die annually as a result of non-communicable diseases (NCDs), accounting for 71% of all deaths worldwide [1]. Similar results were reported in the 2012 Korean Burden of Disease Study [2]. In terms of disease burden, NCDs made a greater contribution to years lived with disability than to premature death [2]. As a result of the nature of NCDs, long-term treatment and care are required, which can affect the patients’ quality of life. In addition, the aging population will further increase the NCD burden. Therefore, amelioration and prevention of NCDs are important goals.
Longitudinal studies have suggested that the origin of NCDs in adulthood can be traced to early life [3,4]. The Bogalusa Heart Study began in 1972 in children aged 5-17 years and evaluated early-life risk factors for cardiovascular health. In that study, uric acid levels in childhood were predictive of high blood pressure in childhood and adulthood [5], and childhood blood pressures were reflected in adulthood [3]. The cumulative evidence for the long-term effects of early life on adult health implies the need for a birth cohort study [6]. In England, the Avon Longitudinal Study of Parents and Children began collecting genotype and environmental characteristics data on 13,761 pregnant women in the early 1990s, and collection of follow-up data is ongoing [7]. The Norwegian Mother and Child Cohort Study began recruiting pregnant women in 1999 and 2005 [8], and Project VIVA recruited pregnant women in 1999 to 2002 in eastern Massachusetts in the United States and in mid-2010 followed-up the offspring, who were then in their early teens [9]. Some epidemiological studies have reported results related to early-life risks for health later in life, but there were few relevant studies in Korea at that time. Accordingly, the Ewha Birth and Growth Study was designed to evaluate factors affecting growth and health in childhood, with a focus on cardiometabolic health. Here, we introduce the Ewha Birth and Growth Study and describe the main findings.
Description of the cohort and follow-up
Obstetricians, pediatricians, and experts in anatomy, epidemiology, and nutrition were involved in constructing the cohort. From September 2001 to June 2006, investigators recruited participants from those who visited the Ewha Womans University Mokdong Hospital (a tertiary hospital in southwest Seoul, Korea) for prenatal care at 24 weeks to 28 weeks of gestation. About 30% of all eligible women agreed to participate in the study and provide information at delivery [10]. A total of 891 women participated in this study, and their children (n= 940) were followed-up.
Follow-up postal surveys were conducted at 6 months, 12 months, 18 months, and 24 months, and regular check-up examinations were conducted at 3 years, 5 years, and 7 years of age and annually thereafter (Figure 1). In 2015, check-up examinations at 13 years of age were begun. Check-up examinations at the ages of 14 years and 15 years were performed for subjects who did not receive check-ups at 13 years or 14 years of age. To overcome the reduction in sample size caused by the low follow-up rate, subjects born in the same hospital who visited the pediatric department at the age of 3 years were enrolled and followed-up. At the time of each follow-up, we informed the parents or guardians by telephone about the check-up examination. About half of the subjects were contacted, and about 75% participated in the regular check-up examinations. The children and their parents or guardians visited the hospital and the children fasted overnight for at least 8 hours. To minimize temporal and seasonal variations, we performed the follow-up examinations in the morning and at similar times of year. The check-up examinations involved anthropometric measurements, questionnaires, dietary surveys, and blood and urine sampling. Venous blood samples were collected into vacutainer tubes (plasma and serum). Blood and urine samples were stored at -70°C to -80°C until analysis. Individual dietary data were collected by trained dieticians during face-to-face interviews. In 2021, the subjects will reach 19 years of age, and we are planning a check-up examination for early adulthood. Table 1 lists the numbers of participants and anthropometric data across the follow-up visits.
Ethics statement
The study protocol was approved by the Institutional Review Board (IRB) of Ewha Womans University Hospital. During follow-up, the research protocols were updated and reapproved by the IRB of Ewha Womans University Hospital. Because the research institute moved in 2019, a new IRB number was assigned (IRB No. SEUMC 2019-04-035). Written informed consent was obtained from all participants prior to the baseline survey. The parents or guardians of the subjects provided informed consent for participation in check-up examinations. Participants were informed that they could withdraw from the study at any time.
We collected a range of data, including genotypes, from the cohort. Table 2 shows a list of measurements by follow-up time.
At birth, birth weight and body length were measured in the delivery room by trained nurses using digital scales. Gestational age was calculated based on the maternal report of the date of the last menstrual period and an ultrasound measurement performed by an obstetrician. Cord blood and placental tissue were sampled.
Anthropometric data were measured by trained researchers and nurses in the hospital. Height and weight were measured to the nearest 0.1 cm and 0.1 kg, respectively, using a stadiometer and calibrated scale, with the subject wearing light clothing and no shoes. Blood pressure was measured twice by trained researchers using an automatic device of the correct cuff size with participants resting in a stable position. Two measurements, taken within 5 minutes of each other, were averaged. Blood chemistry tests were performed for fasting blood glucose, lipid profile, and liver function enzymes, as well as a complete blood count.
Physical activity and sedentary behavior were assessed using questionnaires. Data on nutrient intake and food intake were collected by dietary survey, by 2 days of 24-hour recall for weekdays or using a food-frequency questionnaire (FFQ). The reproducibility and validity of the FFQ were acceptable [11]. As the subjects entered adolescence, the FFQ tool was modified by expert consensus, by adding 2 beverage items (e.g., coffee). The 24-hour dietary recall survey was conducted by the children’s guardians or parents (most frequently the mother). If children were attending kindergarten, the investigator attempted to contact their kindergarten teachers to collect accurate information. Nutrient intake was determined via CAN-pro version 3.0 (Korean Nutrition Society, Seoul, Korea). Dietary habits were assessed using a validated mini-dietary assessment tool [12]. To assess behavioral problems, we used the Korean version of the Child Behavior Checklist (K-CBCL) [13] and Conner’s Hyperactivity Rating Scale [14]. We also performed evaluations using the Children’s Depression Inventory [15], State-Trait Anxiety Inventory [16], and Trait Anxiety Inventory for Children [17].
At the follow-ups between 7 years and 9 years of age, for puberty evaluation, bone age and Tanner stage were evaluated by X-ray scans and the clinician’s assessment, respectively. Sex-hormone (luteinizing hormone, dehydroepiandrosterone, androstenedione, free testosterone, and free estradiol) concentrations were measured in blood samples. As the subjects entered adolescence, carotid intima-media thickness and endothelial dysfunction biomarkers were measured as indicators of atherosclerosis susceptibility. Carotid intima-media thickness was measured by a trained and certified sonographer.
For genotyping, genetic loci related to homocysteine metabolism (rs1801133 in methylenetetrahydrofolate reductase), the renin–angiotensin system (rs4341 in angiotensin-converting enzyme), and uric acid concentration (rs3825017 in solute carrier family 22 member 12 [SLC22A12] and rs16890979 in solute carrier family 2 facilitated glucose transporter member 9 [SLC2A9]) were identified. If stored cord blood was available, the methylation levels of proopiomelanocortin (POMC), the melanocortin 4 receptor (MC4R), and hepatocyte nuclear factor 4 alpha (HNF4a; associated with metabolic syndrome) were assayed in participants in check-up examinations at the ages of 7-9 years.
As part of a research project, the levels of endocrine disruptors—polychlorinated biphenyl, organochlorine pesticide, bisphenol A (BPA), and phthalates—in stored blood and urine samples were measured by Lab Frontier Co., Ltd. (Anyang, Korea).
About 20 years have passed since the cohort data were collected, and we have published a broad spectrum of results. The findings from the Ewha Birth and Growth Study are listed in Supplemental Material 1 and some of the main findings are described below.
The Ewha Birth and Growth Study evaluated relationships between perinatal exposure, birth characteristics, and childhood health. Mendelian randomization revealed that the explainable homocysteine level during pregnancy due to genetic variants was causally related to birth weight [10]. Birth characteristics affect the variance in metabolic indicators in childhood. Regarding perinatal epigenetic effects, the methylation levels of POMC, MC4R, and HNF4a in cord blood were associated with triglyceride levels in children aged 7-9 years [18,19]. In addition, according to Park et al. [20,21], fetal characteristics are associated with elevated uric acid levels at 3 years of age, and high uric acid levels during the preschool period are associated with elevated blood pressure at the age of 7 years.
Hong et al. [22] reported that maternal micronutrient intake, as measured in blood, was persistently associated with growth during the first 3 years of life. Growth levels were linked to childhood blood pressure and pubertal development. The effect of angiotensin-converting enzyme genotype on blood pressure in childhood varies with postnatal growth [23]. Regarding pubertal development, longitudinal observations from birth to 7-9 years of age showed that weight Z-scores at 5 years of age differed significantly between subjects who did and did not experience early puberty. Postnatal weight changes from birth to 7-9 years of age were independently associated with early puberty. Notably, breastfeeding for 6 months or longer prevented early puberty [24].
Using dietary data collected at the ages of 3 years and 7 years, the relationship between macronutrient intake and lipid metabolism was evaluated [25]. During the 4-year follow-up, increased intake of carbohydrates had an unfavorable effect on triglyceride levels, and increased intake of fat, especially animal-based fat, increased low-density lipoprotein-cholesterol levels over time. Another study using FFQ data identified dietary patterns through principal component analysis and evaluated dietary behaviors associated with a healthier dietary pattern [11]. The dietary patterns—healthy intake, animal food intake, and snack intake—were similar at 7 years and 9 years of age. Changes in behavior that increased the consumption of milk or dairy products or encouraged the consumption of vegetables with every meal had favorable effects on changes in healthy dietary pattern scores over 2 years. These studies have shown that improved eating behavior can benefit childhood diet.
Taking advantage of the repeated measurement data, we evaluated candidate genotypes related to uric acid levels. The rs3825017 genotype of SLC22A12 was associated with a sex difference in uric acid levels during the first 10 years of life; however, the association was significant only in boys [26]. The consistency of the results at all time points supports the validity of the conclusions.
Other studies have assessed the health risks of exposure to endocrine disruptors. At routine low-dose exposure levels, exposure to endocrine disruptors affected metabolic-syndrome-related indicators [27,28], including insulin secretion [29], and was related to liver indices [30] and sex hormone levels [31]. Regarding the critical exposure period, the urinary BPA concentration tertile at 7-9 years, rather than 3-5 years, showed a dose-response relationship with liver enzyme levels at 10-13 years of age [30]. Using phthalate data measured repeatedly at ages 3-5 and 7-9, we evaluated the effect of long-term exposure to phthalates on metabolic indicators. Children with consistently high levels of exposure had high levels of triglycerides and homeostatic model assessment for insulin resistance scores, and low levels of high-density lipoprotein-cholesterol (HDL-c) [28]. Environmental exposure is associated with behavioral development as well as metabolic health in children. Using the K-CBCL data, we evaluated the effect of environmental tobacco smoke exposure (as assessed by cotinine levels) on behavioral problems [32]. High levels of cotinine at the age of 5 years were associated with higher total behavioral problem scores, a link that remained evident until the age of 9 years.
Recently, we started reporting on adolescent health-related research topics. A mediation analysis implied that, among the metabolic syndrome components, body mass index was directly related to elevated high-sensitivity C-reactive protein levels and indirectly via HDL-c to elevated intercellular adhesion molecule 1 levels [33]. The data collected were from young people, and further results are therefore expected to be published.
The Ewha Birth and Growth cohort is a leading long-term follow-up study in Korea. The results from this cohort are consistent with previous findings in other countries. This cohort provides an opportunity to assess the effect of early life on later health, and the findings emphasize the need for interventions in early life to prevent subsequent NCDs.
Nonetheless, several limitations should be kept in mind. Although this cohort study consisted of a general population of children, the generalizability of the results is weakened by the hospital-based recruitment. Furthermore, the follow-up rate was low. Loss to follow-up resulting from moving house, changing telephone numbers, and withdrawal is inevitable in cohort studies. Loss to follow-up can lead to a decrease in the power for exploring the research hypothesis and the reliability of the results. A simulation study found that there was no significant bias until the follow-up loss was up to 60% based on the missing at random or missing completely at random mechanism [34]. As our cohort study considered various exposures in a typical setting and evaluated the outcome prospectively, it is thought that the loss in follow-up was random. Thus, the resulting loss of follow-up measures may affect the reliability of the results, but the direction of the association was consistent with other studies. Finally, the cohort size is smaller than that of other birth cohorts, but we increased the power of the statistical tests by performing repeated measurements.
In our experience, the nature of a prospective cohort study entails long-term follow-up and it is necessary to build a trustful relationship between participants and researchers to prevent follow-up loss and to maintain participation. Long-term follow-up involves not only financial funding, but also maintenance and management of personnel, so a large amount of effort is required to maintain the cohort. In addition, to expand and utilize cohort resources, there is a need to be concerned with health issues along with social trends and to explore potential research questions.
The cohort data are not freely available, but the Ewha Birth and Growth Study team welcomes collaborations with other researchers. For further information, contact Dr. Park (the corresponding author).
Supplementary materials are available at http://www.e-epih.org/.
Supplementary Material 1.
Research hypothesis
epih-43-e2021016-suppl1.docx

CONFLICT OF INTEREST

The authors have no conflicts of interest to declare for this study.

FUNDING

This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) (No. NRF-2020R1F1A1062227).

AUTHOR CONTRIBUTIONS

Conceptualization: EAP, SJC, HL, YJK, EHH, HP. Data curation: EJC, UJK, HJP. Formal analysis: HAL, UJK, HJP. Funding acquisition: HP. Methodology: BP, JM, EAP, SJC, HSK, HL, YJK, YSH, EJK, EHH, HP. Project administration: HP. Visualization: HAL. Writing – original draft: HAL. Writing – review & editing: BP, JM, EJC, UJK, HJP, EAP, SJC, HSK, HL, YJK, YSH, EJK, EHH, HP.

We appreciate the contributions of Professor Se-Young Oh and the nutrition team’s contribution to the successful implementation of the nutrition survey. We also express our gratitude to the many people who assisted with data collection. Finally, our research team is deeply grateful to the children/adolescents and their families who participated in this cohort study.
Figure 1.
The Ewha Birth and Growth Study establishment and follow-up history.
epih-43-e2021016f1.jpg
Table 1.
Summary of the structure of the Ewha Birth and Growth Study1
Characteristics At birth Follow-up examinations (yr)
3 5 7 8 9 10 11 12 13-15
Boys
 No. of subjects 487 236 202 161 199 200 123 133 116 122
 Height (cm) 49.4±2.4 97.8±4.5 112.2±5.3 124.4±5.7 130.3±5.6 135.0±5.7 139.1±6.0 145.8±6.1 152.5±7.8 162.8±7.0
 Z-score of height -0.2±1.3 -0.5±1.2 -0.2±1.2 -0.2±1.1 -0.1±1.1 -0.2±1.0 -0.5±1.0 -0.3±0.9 -0.3±1.1 0.0±0.9
 Weight (kg) 3.2±0.5 14.9±2.0 20.1±3.4 25.3±4.9 29.1±6.3 32.8±6.9 35.5±7.6 41.2±9.4 47.8±11.0 56.0±12.3
 Z-score of weight -0.3±1.2 -0.7±1.3 -0.2±1.3 -0.4±1.2 -0.3±1.2 -0.3±1.1 -0.4±1.1 -0.3±1.1 -0.1±1.1 0.1±1.1
 BMI (kg/m2) 13.2±1.3 15.5±1.4 15.9±1.8 16.2±2.2 17.0±2.7 17.8±2.8 18.2±3.1 19.2±3.2 20.4±3.4 21.1±3.8
 Overweight2 - 12 (5.2) 13 (6.4) 11 (6.9) 14 (7.1) 16 (8.1) 12 (9.8) 11 (8.3) 8 (7.7) 5 (5.1)
 Obesity3 - 13 (5.7) 16 (7.9) 11 (6.9) 18 (9.1) 16 (8.1) 7 (5.7) 10 (7.5) 13 (12.5) 12 (12.1)
 SBP (mmHg) 65.8±8.1 93.8±10.5 93.8±10.5 100.8±9.8 106.0±10.8 107.7±10.9 110.2±11.7 111.8±10.0 110.0±13.5 111.8±11.8
 DBP (mmHg) 39.2±8.0 60.2±9.6 59.2±6.6 58.4±6.7 61.1±6.9 63.1±6.6 69.8±8.9 69.6±8.4 68.7±8.3 68.3±9.2
 High BP4 - - - 6 (3.8) 4 (2.0) 7 (3.5) 4 (3.3) 5 (3.8) 4 (3.5) 3 (2.5)
Girls
 No. of subjects 452 239 196 201 183 199 113 143 113 127
 Height (cm) 48.7±2.7 96.1±4.2 111.5±4.7 122.8±4.9 129.9±5.0 134.7±5.7 139.2±5.7 147.0±6.3 153.6±6.1 158.2±5.4
 Z-score of height -0.3±1.4 -0.7±1.1 0.0±1.1 -0.2±1.0 0.0±0.9 -0.2±1.0 -0.5±0.9 -0.3±1.0 0.0±1.0 0.1±1.0
 Weight (kg) 3.1±0.5 14.3±1.7 19.4±2.8 23.9±4.1 28.2±5.3 31.4±5.9 34.8±7.2 40.3±7.6 46.3±8.5 51.1±8.3
 Z-score of weight -0.3±1.3 -0.7±1.2 -0.2±1.2 -0.4±1.1 -0.2±1.0 -0.3±1.0 -0.4±1.0 -0.3±1.0 0.0±1.0 0.1±1.0
 BMI (kg/m2) 13.1±1.5 15.4±1.3 15.5±1.5 15.8±2.1 16.6±2.5 17.2±2.4 17.8±2.7 18.6±2.8 19.6±3.0 20.4±2.9
 Overweight2 - 19 (8.2) 11 (5.6) 8 (4.0) 13 (7.1) 19 (9.6) 9 (8.0) 7 (4.9) 13 (13.8) 15 (11.8)
 Obesity3 - 11 (4.7) 8 (4.1) 10 (5.0) 9 (4.9) 7 (3.5) 8 (7.1) 9 (6.3) 7 (7.5) 9 (7.1)
 SBP (mmHg) 68.2±9.4 93.5±9.5 98.5±9.4 99.1±10.1 103.1±11.4 105.6±10.6 109.8±10.8 111.6±11.0 108.9±11.5 108.7±11.1
 DBP (mmHg) 39.3±8.0 60.3±8.9 59.3±6.4 59.2±6.8 60.5±7.3 62.4±7.4 69.5±8.0 71.0±9.3 68.5±8.8 66.9±7.9
 High BP4 - - - 1 (0.5) 2 (1.1) 5 (2.5) 1 (0.9) 2 (1.4) 0 (0.0) 2 (1.6)

Values are presented as mean±standard deviation or number (%).

The sex- and age-specific Z-scores of height and weight were calculated based on the 2017 Korean Children and Adolescent National Growth Charts; Overweight and obesity were defined based on the 2017 Korean Children and Adolescent National Growth Charts; High BP was defined based on the 2007 Korean Children and Adolescent National Growth Charts.

BMI, body mass index; SBP, systolic blood pressure; DBP, diastolic blood pressure; BP, blood pressure.

1 Numbers vary as a result of missing data.

2 Overweight: 85th ≤ BMI < 95th percentile.

3 Obesity: BMI ≥ 95th percentile or BMI ≥25.0 kg/m2.

4 High BP: SBP or DBP ≥ 90th percentile or SBP/DBP ≥120/80 mmHg.

Table 2.
Summary of measured phenotypes in the Ewha Birth and Growth Study
Phenotype At birth Follow-up examinations
6 mo1 12 mo1 18 mo1 24 mo1 3 yr 5 yr 7 yr 8 yr 9 yr 10 yr 11 yr 12 yr 13-15 yr
Questionnaires
  Demographics O2 O2 O2 O2 O O O O O O O O O
Breastfeeding O2 O2 O2 O2 O O O O O - - - -
Physical activity O2 O2 O2 O2 O O O O O - O O O
Parental disease history (HTN, DM, stroke, etc.) - - - - O O O O O - O O O
Secondhand smoking O2 O2 O2 O2 O O O O O O O O O
K-CBCL - - - - - O O - O - O2 O -
Conners Hyperactivity Rating Scale - - - - - O O - O - O O -
ADHD - - - - - O O - O - O O -
CDI, STAI, and TAIC - - - - - - - - O2 - O2 O2 -
Pubertal status (Tanner stage) - - - - - - O O O O O O O
Nutrition survey
Diet (24-hr recall) - - - - O O2 O - - - - - -
Diet (FFQ) - - - - - O2 O O O O O O O
Eating behaviors - - - - O - O O O O O O O
Physical examination
Anthropometric O2 O2 O2 O2 O O O O O O O O O
Blood pressure - - - - O O O O O O O O O
Hand-grip strength - - - - - - O O O - - - -
Bone mineral density - - - - - O2 - O2 O2 - - - -
Body composition (muscle, % body fat, etc.) - - - - O2 O O2 O O - - - -
Bone age - - - - - - O2 O2 O2 - - - -
Carotid intima-media thickness - - - - - - - - - - - - O
Blood
Chemistries - - - - O O O O O O O O O
Liver enzymes (gamma-glutamyl transferase) - - - - - - - - - O O O O
Persistent organic pollutants - - - - - - O2 O2 O2 - - - -
Lipids (total cholesterol, triglyceride, high-density lipoprotein cholesterol) - - - - O O O O O O O O O
Glucose - - - - O O O O O O O O O
Insulin - - - - O2 O O O O O2 O2 - O
Uric acid - - - - O2 O O O O O O O O
Endothelial dysfunction (ICAM-1, VCAM-1) - - - - - - - - - - - - O
Inflammatory biomarkers (hs-CRP, IL-6) - - - - O2 O O O O - - - O
Sex hormones (luteinizing hormone, DHEA, androstenedione, testosterone, estradiol) - - - - - - O O2 O2 - - - -
Thyroid-stimulating hormone - - - - - - O2 O2 O2 O O O O
Free thyroxine (fT4) - - - - - - O2 O2 O2 O2 O2 O2 -
25-Hydroxyvitamin D - - - - - - O O O - - - -
Oxidative stress
8-OHdG - - - - O2 O2 O2 - - - - - -
MDA - - - - O2 O2 O2 - - - - - -
Vitamins
Vitamin C - - - - O2 - - - - - - - -
Retinol - - - - O2 - - - - - - - -
Tocopherol - - - - O2 - - - - - - - -
Carotene - - - - O2 - - - - - - - -
Methylation
Proopiomelanocortin - - - - - - O2 O2 O2 - - - -
Hepatocyte nuclear factor 4 alpha - - - - - - O2 O2 O2 - - - -
Melanocortin 4 receptor - - - - - - O2 O2 O2 - - - -
Urine
Cotinine - - - - O2 O O - - - - - -
Bisphenol A - - - - O O O O2 O - - - -
Phthalate metabolites - - - - O2 O2 O2 O2 O2 - - - -
Single-nucleotide polymorphisms Glutathione S-transferase T1
Glutathione S-transferase M1
Angiotensin-converting enzyme rs4341
Paraoxonase 1 rs662
Myeloperoxidase rs2333227
Peroxisome proliferator-activated receptor gamma rs1801282
Fat mass and obesity‐associated rs9939609
Solute carrier family 2 facilitated glucose transporter member 9 rs16890979
Solute carrier family 22 member 12 rs3825017

HTN, hypertension; DM, diabetes mellitus; K-CBCL, Korean-Childhood Behavioral Checklist; ADHD, attention deficit hyperactivity disorder; CDI, Children’s Depression Inventory; STAI, State-Trait Anxiety Inventory; TAIC, Trait Anxiety Inventory for Children; FFQ, food frequency questionnaire; ICAM-1, intercellular adhesion molecule; VCAM-1, vascular cell adhesion molecule 1; hs-CRP, high-sensitivity C-reactive protein; IL, Interleukin; DHEA, dehydroepiandrosterone; MDA, malondialdehyde, 8-OHdG, 8-hydroxy-2′-deoxyguanosine.

1 Follow-up examinations were conducted by mail.

2 Only a portion of the subjects was measured.

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Figure & Data

References

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    Figure
    • 0
    Cohort profile: the Ewha Birth and Growth Study
    Image
    Figure 1. The Ewha Birth and Growth Study establishment and follow-up history.

    Figure 1.

    Cohort profile: the Ewha Birth and Growth Study
    Characteristics At birth Follow-up examinations (yr)
    3 5 7 8 9 10 11 12 13-15
    Boys
     No. of subjects 487 236 202 161 199 200 123 133 116 122
     Height (cm) 49.4±2.4 97.8±4.5 112.2±5.3 124.4±5.7 130.3±5.6 135.0±5.7 139.1±6.0 145.8±6.1 152.5±7.8 162.8±7.0
     Z-score of height -0.2±1.3 -0.5±1.2 -0.2±1.2 -0.2±1.1 -0.1±1.1 -0.2±1.0 -0.5±1.0 -0.3±0.9 -0.3±1.1 0.0±0.9
     Weight (kg) 3.2±0.5 14.9±2.0 20.1±3.4 25.3±4.9 29.1±6.3 32.8±6.9 35.5±7.6 41.2±9.4 47.8±11.0 56.0±12.3
     Z-score of weight -0.3±1.2 -0.7±1.3 -0.2±1.3 -0.4±1.2 -0.3±1.2 -0.3±1.1 -0.4±1.1 -0.3±1.1 -0.1±1.1 0.1±1.1
     BMI (kg/m2) 13.2±1.3 15.5±1.4 15.9±1.8 16.2±2.2 17.0±2.7 17.8±2.8 18.2±3.1 19.2±3.2 20.4±3.4 21.1±3.8
     Overweight2 - 12 (5.2) 13 (6.4) 11 (6.9) 14 (7.1) 16 (8.1) 12 (9.8) 11 (8.3) 8 (7.7) 5 (5.1)
     Obesity3 - 13 (5.7) 16 (7.9) 11 (6.9) 18 (9.1) 16 (8.1) 7 (5.7) 10 (7.5) 13 (12.5) 12 (12.1)
     SBP (mmHg) 65.8±8.1 93.8±10.5 93.8±10.5 100.8±9.8 106.0±10.8 107.7±10.9 110.2±11.7 111.8±10.0 110.0±13.5 111.8±11.8
     DBP (mmHg) 39.2±8.0 60.2±9.6 59.2±6.6 58.4±6.7 61.1±6.9 63.1±6.6 69.8±8.9 69.6±8.4 68.7±8.3 68.3±9.2
     High BP4 - - - 6 (3.8) 4 (2.0) 7 (3.5) 4 (3.3) 5 (3.8) 4 (3.5) 3 (2.5)
    Girls
     No. of subjects 452 239 196 201 183 199 113 143 113 127
     Height (cm) 48.7±2.7 96.1±4.2 111.5±4.7 122.8±4.9 129.9±5.0 134.7±5.7 139.2±5.7 147.0±6.3 153.6±6.1 158.2±5.4
     Z-score of height -0.3±1.4 -0.7±1.1 0.0±1.1 -0.2±1.0 0.0±0.9 -0.2±1.0 -0.5±0.9 -0.3±1.0 0.0±1.0 0.1±1.0
     Weight (kg) 3.1±0.5 14.3±1.7 19.4±2.8 23.9±4.1 28.2±5.3 31.4±5.9 34.8±7.2 40.3±7.6 46.3±8.5 51.1±8.3
     Z-score of weight -0.3±1.3 -0.7±1.2 -0.2±1.2 -0.4±1.1 -0.2±1.0 -0.3±1.0 -0.4±1.0 -0.3±1.0 0.0±1.0 0.1±1.0
     BMI (kg/m2) 13.1±1.5 15.4±1.3 15.5±1.5 15.8±2.1 16.6±2.5 17.2±2.4 17.8±2.7 18.6±2.8 19.6±3.0 20.4±2.9
     Overweight2 - 19 (8.2) 11 (5.6) 8 (4.0) 13 (7.1) 19 (9.6) 9 (8.0) 7 (4.9) 13 (13.8) 15 (11.8)
     Obesity3 - 11 (4.7) 8 (4.1) 10 (5.0) 9 (4.9) 7 (3.5) 8 (7.1) 9 (6.3) 7 (7.5) 9 (7.1)
     SBP (mmHg) 68.2±9.4 93.5±9.5 98.5±9.4 99.1±10.1 103.1±11.4 105.6±10.6 109.8±10.8 111.6±11.0 108.9±11.5 108.7±11.1
     DBP (mmHg) 39.3±8.0 60.3±8.9 59.3±6.4 59.2±6.8 60.5±7.3 62.4±7.4 69.5±8.0 71.0±9.3 68.5±8.8 66.9±7.9
     High BP4 - - - 1 (0.5) 2 (1.1) 5 (2.5) 1 (0.9) 2 (1.4) 0 (0.0) 2 (1.6)
    Phenotype At birth Follow-up examinations
    6 mo1 12 mo1 18 mo1 24 mo1 3 yr 5 yr 7 yr 8 yr 9 yr 10 yr 11 yr 12 yr 13-15 yr
    Questionnaires
      Demographics O2 O2 O2 O2 O O O O O O O O O
    Breastfeeding O2 O2 O2 O2 O O O O O - - - -
    Physical activity O2 O2 O2 O2 O O O O O - O O O
    Parental disease history (HTN, DM, stroke, etc.) - - - - O O O O O - O O O
    Secondhand smoking O2 O2 O2 O2 O O O O O O O O O
    K-CBCL - - - - - O O - O - O2 O -
    Conners Hyperactivity Rating Scale - - - - - O O - O - O O -
    ADHD - - - - - O O - O - O O -
    CDI, STAI, and TAIC - - - - - - - - O2 - O2 O2 -
    Pubertal status (Tanner stage) - - - - - - O O O O O O O
    Nutrition survey
    Diet (24-hr recall) - - - - O O2 O - - - - - -
    Diet (FFQ) - - - - - O2 O O O O O O O
    Eating behaviors - - - - O - O O O O O O O
    Physical examination
    Anthropometric O2 O2 O2 O2 O O O O O O O O O
    Blood pressure - - - - O O O O O O O O O
    Hand-grip strength - - - - - - O O O - - - -
    Bone mineral density - - - - - O2 - O2 O2 - - - -
    Body composition (muscle, % body fat, etc.) - - - - O2 O O2 O O - - - -
    Bone age - - - - - - O2 O2 O2 - - - -
    Carotid intima-media thickness - - - - - - - - - - - - O
    Blood
    Chemistries - - - - O O O O O O O O O
    Liver enzymes (gamma-glutamyl transferase) - - - - - - - - - O O O O
    Persistent organic pollutants - - - - - - O2 O2 O2 - - - -
    Lipids (total cholesterol, triglyceride, high-density lipoprotein cholesterol) - - - - O O O O O O O O O
    Glucose - - - - O O O O O O O O O
    Insulin - - - - O2 O O O O O2 O2 - O
    Uric acid - - - - O2 O O O O O O O O
    Endothelial dysfunction (ICAM-1, VCAM-1) - - - - - - - - - - - - O
    Inflammatory biomarkers (hs-CRP, IL-6) - - - - O2 O O O O - - - O
    Sex hormones (luteinizing hormone, DHEA, androstenedione, testosterone, estradiol) - - - - - - O O2 O2 - - - -
    Thyroid-stimulating hormone - - - - - - O2 O2 O2 O O O O
    Free thyroxine (fT4) - - - - - - O2 O2 O2 O2 O2 O2 -
    25-Hydroxyvitamin D - - - - - - O O O - - - -
    Oxidative stress
    8-OHdG - - - - O2 O2 O2 - - - - - -
    MDA - - - - O2 O2 O2 - - - - - -
    Vitamins
    Vitamin C - - - - O2 - - - - - - - -
    Retinol - - - - O2 - - - - - - - -
    Tocopherol - - - - O2 - - - - - - - -
    Carotene - - - - O2 - - - - - - - -
    Methylation
    Proopiomelanocortin - - - - - - O2 O2 O2 - - - -
    Hepatocyte nuclear factor 4 alpha - - - - - - O2 O2 O2 - - - -
    Melanocortin 4 receptor - - - - - - O2 O2 O2 - - - -
    Urine
    Cotinine - - - - O2 O O - - - - - -
    Bisphenol A - - - - O O O O2 O - - - -
    Phthalate metabolites - - - - O2 O2 O2 O2 O2 - - - -
    Single-nucleotide polymorphisms Glutathione S-transferase T1
    Glutathione S-transferase M1
    Angiotensin-converting enzyme rs4341
    Paraoxonase 1 rs662
    Myeloperoxidase rs2333227
    Peroxisome proliferator-activated receptor gamma rs1801282
    Fat mass and obesity‐associated rs9939609
    Solute carrier family 2 facilitated glucose transporter member 9 rs16890979
    Solute carrier family 22 member 12 rs3825017
    Table 1. Summary of the structure of the Ewha Birth and Growth Study1

    Values are presented as mean±standard deviation or number (%).

    The sex- and age-specific Z-scores of height and weight were calculated based on the 2017 Korean Children and Adolescent National Growth Charts; Overweight and obesity were defined based on the 2017 Korean Children and Adolescent National Growth Charts; High BP was defined based on the 2007 Korean Children and Adolescent National Growth Charts.

    BMI, body mass index; SBP, systolic blood pressure; DBP, diastolic blood pressure; BP, blood pressure.

    Numbers vary as a result of missing data.

    Overweight: 85th ≤ BMI < 95th percentile.

    Obesity: BMI ≥ 95th percentile or BMI ≥25.0 kg/m2.

    High BP: SBP or DBP ≥ 90th percentile or SBP/DBP ≥120/80 mmHg.

    Table 2. Summary of measured phenotypes in the Ewha Birth and Growth Study

    HTN, hypertension; DM, diabetes mellitus; K-CBCL, Korean-Childhood Behavioral Checklist; ADHD, attention deficit hyperactivity disorder; CDI, Children’s Depression Inventory; STAI, State-Trait Anxiety Inventory; TAIC, Trait Anxiety Inventory for Children; FFQ, food frequency questionnaire; ICAM-1, intercellular adhesion molecule; VCAM-1, vascular cell adhesion molecule 1; hs-CRP, high-sensitivity C-reactive protein; IL, Interleukin; DHEA, dehydroepiandrosterone; MDA, malondialdehyde, 8-OHdG, 8-hydroxy-2′-deoxyguanosine.

    Follow-up examinations were conducted by mail.

    Only a portion of the subjects was measured.

    Table 1.

    Table 2.

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