Literature DB >> 36130760

Cohort profile: maternal antecedents of adiposity and studying the transgenerational role of hyperglycaemia and insulin (MAASTHI).

Eunice Lobo1, Yamuna Ana1, R Deepa1, Prafulla Shriyan1, N D Sindhu1, Maithili Karthik1, Sanjay Kinra2, G V S Murthy3, Giridhara R Babu4,5.   

Abstract

PURPOSE: The Maternal Antecedents of Adiposity and Studying the transgenerational role of Hyperglycaemia and Insulin cohort in Bengaluru, South India, aims to understand the transgenerational role of increased circulating glucose levels or hyperglycaemia and other nutrients and psychosocial environment, on the risk of childhood obesity, as an early marker of chronic diseases. PARTICIPANTS: Through this paper, we describe the baseline characteristics of the cohort participants and their children, along with plans and challenges. A total of 5694 pregnant women were screened, with 4862 (85.4%) eligible pregnant women recruited at baseline. We assessed anthropometry, Haemoglobin status, Oral Glucose Tolerance Test (OGTT), dietary practices, depressive symptoms using the Edinburgh Postnatal Depression Scale and social support in all women. Follow-up visits involved assessing anthropometry and the health profile of mothers and children. FINDINGS TO DATE: Among 4862 eligible participants recruited, 3260 (67%) underwent OGTT, while 2962 participants completed OGTT (90.9%). During the pregnancy, 9.7% of women were obese (>90th percentile of skinfold thickness), and 14.3% had gestational diabetesmellitus. Moreover, 6.2% and 16.8% of women had symptoms suggestive of depression during pregnancy and the immediate postnatal period, respectively. We found that 3.3% of children were small for gestational age, 10.8% were large for gestational age and 9.7% of children were obese at birth. FUTURE PLANS: We have completed recruitment and baseline data collection in 2019, and are conducting annual follow-ups until age 4 of the participant's children. For delineating causal pathways of childhood obesity, blood aliquots are stored in the biorepository. The study will inform policy formulation and community awareness in the prevention and control of non-communicable diseases and health promotion. © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.

Entities:  

Keywords:  DIABETES & ENDOCRINOLOGY; EPIDEMIOLOGY; Health policy; PUBLIC HEALTH

Mesh:

Substances:

Year:  2022        PMID: 36130760      PMCID: PMC9494597          DOI: 10.1136/bmjopen-2022-063794

Source DB:  PubMed          Journal:  BMJ Open        ISSN: 2044-6055            Impact factor:   3.006


Maternal Antecedents of Adiposity and Studying the transgenerational role of Hyperglycaemia and Insulin is a well-established cohort study documenting the life course trajectory in the genesis of non-communicable diseases (NCDs) for important exposure contrasts experienced by women very early on in their pregnancy and continues to document the outcomes across the process of pregnancy, childbirth, and early childhood, including assessing important milestones of the child. This is the largest prospective birth cohort in the urban public sector on maternal and child health in South India, with a large sample size over a relatively long period of follow-up. Blood aliquots are stored in the biorepository for future studies on childhood obesity. Operational issues in terms of incomplete oral glucose tolerance test and lost to follow-up after delivery are the limitations of conducting a study in public health facilities. Our cohort will inform policy formulation and community awareness in the prevention and control of NCDs and health promotion.

Introduction

According to the recent global disease burden study, type 2 diabetes mellitus (T2DM) is the fifth most common disease affecting Indians.1 T2DM is projected to affect 70 million Indians by the year 20252–7 at a relatively younger age compared with high-income countries. The increasing prevalence of gestational diabetes mellitus (GDM) directly impacts the T2DM burden.6 Findings from the Hyperglycaemia and Adverse Pregnancy Outcome study initially confirmed the association between maternal glucose levels and neonatal adiposity.8–11 These results conform to the theoretical frameworks of ‘fuel-mediated teratogenesis’, ‘thrifty phenotype’ and thrifty genotype’ hypotheses,2 8 11–15 which explain the transgenerational nature of obesity-hyperglycaemia. Even the Parthenon Birth cohort and others16–18 have provided initial pieces of evidence regarding this association from low-income and middle-income countries (LMICs). Thus, it becomes necessary to update the recent findings and, more importantly, capture the evidence from resource-constrained, high-burden countries such as India. Given the rapid demographical and epidemiological transition in India, there is a pressing need to capture the evidence on the obesity-hyperglycaemia burden.19 In LMICs, children who have low birth weight (LBW) and early undernutrition are known to have rebound adiposity during early adolescence.20 Therefore, it is important to capture the life course trajectories of the underweight and obesity-led hyperglycaemia epidemics in LMICs. The risk factors of LBW may also be modifiable to prevent ensuing obesity epidemics in these countries. Among these risk factors, undernutrition in pregnancy affects nearly 28% of newborns having LBW in South Asia.21 22 Evidence including high-income countries suggests a putative role in the psychosocial environment and weight of the newborn.23 24 In addition, a recent systematic review also showed similar results for LMICs, with risk factors including poor social support, history of common mental disorders, etc.25 Individual and household stressors frequent exposure leads to poor mental health, including depression and anxiety.26 The mother’s poor mental health throughout pregnancy or after delivery affects mother–child interactions and makes it more difficult for child upbringing.27 The effect of maternal mental health on child growth is likely to be more apparent in low socioeconomic situations due to the relative lack of resources and challenging contextual factors that are associated with poverty. Aligned with the evidence from the high-income countries, we piloted the feasibility of conducting a multi-centric cohort study in the urban public health facilities of Bengaluru. Informed from the results of the pilot study,28 the principal investigator (GRB) obtained funding to set up a birth cohort titled ‘Maternal Antecedents of Adiposity and Studying the transgenerational role of Hyperglycaemia and Insulin’ (MAASTHI). The primary objective of the cohort is to investigate the effect of glucose levels in pregnancy on skinfold thickness (SFT) (adiposity) in infancy as a marker of future obesity and diabetes in offspring, while the secondary objective is to assess the association between the psychosocial environment of mothers and adverse neonatal outcomes including adiposity. By capturing evidence from the mothers and children of low-income and middle-income status visiting health facilities in the public sector, MAASTHI will provide a contextual evidence base resulting in obesity-hyperglycaemia in India.9 28

Cohort description

Study design, sample size, study site and participants

We started the recruitment in the prospective cohort study in April 2016 in the urban public health facilities of Bengaluru, a metropolitan city with a 13 million population in South India. The study protocol with the details of recruitment and methodology is published elsewhere.29 With the assumption of a 5% incidence of childhood obesity at birth in India, a relative risk of 1.5 in the hyperglycaemic group, our estimated sample size with 80% power required to detect a difference at a 95% confidence level was 2936 participants. Considering lost to follow-up by about 60%, we had aimed to recruit 5000 pregnant women. We started recruitment in a 300-bedded public health facility (Jayanagar General Hospital) in Bengaluru corporation. The cohort is established in 14 public health facilities in Bengaluru, Karnataka viz. Jayanagar General Hospital, Bagaluru Referral Hospital, Srirampura Referral Hospital, Anjanappa Garden UPHC, Banashankari Referral Hospital, Bapuji Nagar UPHC, D J Halli UPHC, KC General Hospital, Magadi road UPHC, Pantharapalaya UPHC, Robertsonpet UPHC, Siddaiah Referral Hospital, Sirsi Circle UPHC and Tavrekere UPHC. All pregnant women between 14 and 36 weeks of gestation from the ages of 18–45 years visiting the public health facilities were approached to participate in the study. After obtaining written informed consent, we recruited the women only if they planned to deliver in the study health facility and were available for future follow-ups in Bengaluru. Exclusion criteria included a history of major co-existing diseases as HIV/ADIS, hepatitis B, diabetes and the inability to complete the oral glucose tolerance test (OGTT) within 24–36 weeks of gestation.

Patient and public involvement

No patient involvement.

Data collection

Recruitment and follow-up

We approached 5694 pregnant women and collected the baseline data from 4862 eligible pregnant women and 2873 women who delivered during the period of April 2016–June 2019. A brief overview of study recruitment, retention and at-birth follow-up is presented in figure 1.
Figure 1

Study recruitment and follow-ups in the MAASTHI cohort in India, 2016–2019. The flow chart shows the recruitment to follow-up of participants into the MAASTHI cohort and the reasons for drop-out. MAASTHI, Maternal Antecedents of Adiposity and Studying the transgenerational role of Hyperglycaemia and Insulin; OGTT, Oral Glucose Tolerance Test.

Study recruitment and follow-ups in the MAASTHI cohort in India, 2016–2019. The flow chart shows the recruitment to follow-up of participants into the MAASTHI cohort and the reasons for drop-out. MAASTHI, Maternal Antecedents of Adiposity and Studying the transgenerational role of Hyperglycaemia and Insulin; OGTT, Oral Glucose Tolerance Test. After obtaining written informed consent, eligible pregnant women were recruited into the study when they completed 14 weeks of gestational age, and face-to-face interviews were done by trained research assistants ensuring privacy and confidentiality.

What has been measured?

We have collected sociodemographic details, 24-hour dietary recall, dietary habits, use of tobacco and alcohol (own and spouse) and physical activity in the women. In addition to obtaining a family history of diabetes and other cardiovascular diseases, we obtained an obstetric history from all the pregnant women (table 1). In addition, we have assessed the psychosocial environment using validated versions of the Edinburgh Postnatal Depression Scale (EPDS) and social support scale.30 Between 24 and 36 weeks, all the women were invited to undergo OGTT. GDM was classified using the WHO diagnostic criteria.31 We also measured blood pressure (BP), assessed body mass index (BMI) and measured haemoglobin in all the women (table 1).
Table 1

Assessments and data collected among the participants of MAASTHI birth cohort, Bengaluru 2016

TimeVariable
Mother: 14–36 weeksSociodemographic detailsFamily medical historyPhysical activityTobacco/alcohol use (self and spouse)Dietary habits/24-hour recallObstetrics historyAssessment of depressive symptoms (using EPDS) and social supportMedications/supplements takenBlood pressureAnthropometry measurements

Weight

Height

Biceps skinfold thickness

Triceps skinfold thickness

Subscapular skinfold thickness

Head circumference

Mid upper arm circumference (MUAC)

24–36 weeksOGTT (fasting plasma glucose, 2-hour postprandial plasma glucose) haemoglobin
At deliveryDelivery detailsMother’s weightCause of death, if anyRandom blood sugar for GDM womenInitiation of breastfeeding and feeding practiceAssessment of depressive symptoms (using EPDS)
Postdelivery—14 weeks, 1, 2, 3, 4 yearsHealth statusMedications/supplements takenBody mass index (BMI)Blood pressureAssessment of depressive symptoms (using EPDS)Social supportAnthropometry measurements

Weight

Waist circumference

Hip circumference

Biceps skinfold

Triceps skinfold

Subscapular skinfold

Child: At birth, 14th week, 1, 2, 3, 4 yearsBMIAnthropometry measurements

Weight

Length

Crown-rump length (birth to 1 year)

Head circumference

Chest circumference

Waist circumference

Hip circumference

MUAC

Biceps skinfold thickness

Triceps skinfold thickness

Subscapular skinfold thickness

Infant data and neonatal problemsMorbidity/disease/neonatal intensive care unit/paediatric intensive care unit admissionsImmunisation recordsMedications and supplement useDietMilk or formula feedingIntroduction of complementary food and reasonCessation of breast feeding and reason
14 weeks, 1, 2, 3, 4 yearsTrivandrum developmental screening chart
2 yearsToddler feeding practiceModified checklist for autism in toddlersPhysical activity

Fasting plasma glucose equal to or more than 92 mg/dL or 2-hour postprandial plasma glucose equal to or more than 152 mg/dL(32) as GDM.

BMI, body mass index; EPDS, Edinburgh Postnatal Depression Scale; GDM, gestational diabetes mellitus; MAASTHI, Maternal Antecedents of Adiposity and Studying the transgenerational role of Hyperglycaemia and Insulin; OGTT, Oral Glucose Tolerance Test.

Assessments and data collected among the participants of MAASTHI birth cohort, Bengaluru 2016 Weight Height Biceps skinfold thickness Triceps skinfold thickness Subscapular skinfold thickness Head circumference Mid upper arm circumference (MUAC) Weight Waist circumference Hip circumference Biceps skinfold Triceps skinfold Subscapular skinfold Weight Length Crown-rump length (birth to 1 year) Head circumference Chest circumference Waist circumference Hip circumference MUAC Biceps skinfold thickness Triceps skinfold thickness Subscapular skinfold thickness Fasting plasma glucose equal to or more than 92 mg/dL or 2-hour postprandial plasma glucose equal to or more than 152 mg/dL(32) as GDM. BMI, body mass index; EPDS, Edinburgh Postnatal Depression Scale; GDM, gestational diabetes mellitus; MAASTHI, Maternal Antecedents of Adiposity and Studying the transgenerational role of Hyperglycaemia and Insulin; OGTT, Oral Glucose Tolerance Test. The follow-up visits began soon after the delivery. We recorded the health status, morbidities or any other illness of the baby, feeding and mother’s follow-up assessments. The measurements of SFT, circumferences and weight, length in infants were taken at birth and 14 weeks, corresponding to the child’s immunisation visits to the public health facility. Further follow-up visits of the children include anthropometric assessment annually at ages 1, 2, 3 and 4; along with other assessments mentioned in table 1. We use the support from frontline health workers in the community to remind and help track the unavailable participants for follow-up visits. In addition, the research staff regularly call the participants for reminders regarding the follow-up schedule, and if required, also do house visits (after prior permission). These additional efforts are done for participants who cannot visit the public health facility during the defined period. To make it easier for participants, we also schedule follow-up visits in the primary health centres and Anganwadi centres near their residence. We have also examined the role of an interactive voice-based response system (IVRS) and an information workshop in improving the follow-up rates in these women.32 Through IVRS, women received a 2–3 min call to inform them about OGTT test dates, collect their laboratory test reports, and remind them of their follow-up visits. The IVRS also provided health information on GDM, breast feeding and immunisation. A mother and baby Affairs workshop or antenatal workshop and counselling for parents were conducted. This included a lunch for the participant and her family (husband and children, if any). Generally, this is called ‘Seemantha’ in Kannada, similar to a baby shower in other parts of the world. The workshop included a brief talk by health professionals on the importance of GDM screening and management and other antenatal and postnatal topics.

Storage of blood samples for future analysis

At 24–36 weeks, during the collection of blood for OGTT, we collect 11 mL venous blood samples in the fasting state and 2 mL for postprandial blood glucose analysis. The blood is collected in three vacutainers; plain (6 mL for storage), EDTA (3 mL for haemoglobin analysis), and sodium fluoride vacutainers (2 mL each for glucose analysis in fasting and postprandial), respectively. Blood samples are centrifuged and transferred to cryovials within an hour of collecting in cool boxes to a single central laboratory for assays with external quality assurance mechanisms.

Measurements

We perform anthropometric measurements of mothers at the baseline and during subsequent follow-up visits. The weight was measured using Tanita weighing scale, and height using the SECA 213 portable stadiometer. The mother’s BP is measured using the automated digital device (Omron Digital BP measuring device). The anthropometric measurements of the baby are recorded within 72 hours of delivery. Newborn anthropometry was performed using SECA 354 Weighing Scale and SECA 417 infantometer. We measure the head, mid-upper arm, chest and waist circumferences in both the mother and child using Chasmors body circumference tape. The sum of SFT (biceps, triceps and subscapular) (SFT) is measured on the left side of the body using the Holtain Callipers (Holtain, UK).

Quality control

Research assistants were trained and certified by St. Johns Research Institute, Bengaluru, in anthropometric measurements. Strict protocols are followed to maintain accuracy, with the addition of interobserver and intraobserver reliability of measurements assessed at the outset followed by annual certification by the same institute. Trained phlebotomists collect venous blood for laboratory investigations. Biochemical assays are conducted at a central nationally accredited laboratory with internal and external quality checks. Calibration of all the equipments is done every month using prescribed guidelines, with a calibration log maintained by the research staff and supervised by the principal investigator of the study.

Data management and analysis

Data are entered on android tablets regularly using the application specifically designed for the study. The details of the development and use are published elsewhere.33 The primary data collected is exported through MS Excel 2010 and checked periodically by senior team members for data entry errors and missing information. For this paper, the exported data were then cleaned, and explorative data analysis was done to understand and summarise the variables involved. The descriptive analysis was performed using SPSS V.23. The modified EPDS scores cut-off for defining symptoms suggestive of depression was 13 based on a previous study in Karnataka,34 and social support scores were categorised based on the cut-off score of 24 and above as good(≥24) and poor(<24).30 Adiposity (mother and child) and gestational age (child) weight were classified based on percentiles—using 90th percentile as the cut-off value. Adiposity was considered based on the total sum of SFT (using biceps, triceps and subscapular thickness). At the same time, weight for gestational age was classified considering the weight of children at each gestational age, adjusted for parity and gender.35 The birth weight of children was categorised based on the WHO standards, and preterm births were defined as gestational age less than 37 weeks.36 Anaemia in pregnant women was categorised on the WHO criteria based on haemoglobin concentration: Anaemic when <110 g/L at sea level, and no anaemia when above 100 g/L.37 Hypertension among participants was categorised into: normal (<120/80 mm Hg), prehypertension (120–139/80–89 mm Hg), stage 1 hypertension (140–159/90–99 mm Hg), and stage 2 hypertension (≥160/100 mm Hg).38 BMI of the participants was categorised based on the WHO Asian criteria: underweight (<18.5), normal (18.5–22.9), overweight (23.0–24.9) and obese (>25.0).39 Socioeconomic status was categorised using the modified Kuppuswamy socioeconomic status scale 2017 that classifies socioeconomic status as: lower, middle and upper classes.40

Findings to date and discussion

Among 5694 pregnant women, 85.3% (n=4862) were included in the study based on the eligibility criteria and willingness to participate. A total of 67% of women underwent OGTT (n=3260) as per the schedule between 24 and 36 weeks, with a completion rate of 90.9% (n=2962) (figure 1). At the baseline, the mean age of the pregnant women was 24.25±4.06 years, with 66% between the age group of 18–25 years. Most pregnant women had high school education (66%; n=437). More than 90% of women were homemakers (90.0%; n=4446), while most of their spouses were unskilled workers (46.7%; n=2237%). Using the modified Kuppuswamy scale, most participants were categorised as lower socioeconomic groups (54.6%; n=2614) (table 2).
Table 2

Baseline characteristics of eligible pregnant mothers and children in the MAASTHI birth cohort, Bengaluru, 2016–2021

Maternal characteristics
Sociodemographic characteristicsn (%)
Age (years) (N=4862)
 Mean age±SD24.25±4.06
 18–253211 (66.0)
 26–351598 (32.9)
 36–4553 (1.1)
Religion (N=4862)
 Hindu2454 (50.5)
 Muslim2142 (44.1)
 Others266 (5.5)
Consanguineous marriage (N=4788)1157 (24.2)
Participant’s education (N=4788)
 Illiterate169 (3.5)
 Primary school284 (5.9)
 Middle school609 (12.7)
 High school2091 (43.7)
 PUC or diploma1072 (22.4)
 Graduate and above563 (11.8)
Husband’s education (N=4788)
 Illiterate426 (8.9)
 Primary school461 (9.6)
 Middle school724 (15.1)
 High school1956 (40.9)
 PUC or diploma793 (16.6)
 Graduate and above422 (8.8)
 Do not know6 (0.1)
Participant’s occupation (N=4788)
 Homemaker4446 (92.9)
 Unskilled worker168 (3.5)
 Semiskilled worker76 (1.6)
 Skilled worker85 (1.8)
 Professional13 (0.3)
Husband’s occupation (N=4788)
 Unemployed17 (0.4)
 Unskilled worker2237 (46.7)
 Semiskilled worker1535 (32.1)
 Skilled worker860 (18.0)
 Professional139 (2.9)
Socioeconomic status (N=4788)
 Lower class2614 (54.6)
 Middle class2145 (44.8)
 Upper class29 (0.6)
Chronic conditions with 95% CI of prevalence estimates
Hypertension (N=3719)
 Normal3429 (92.2) (95% CI: 0.91 to 0.93)
 Pre hypertension265 (7.1) (95% CI: 0.69 to 0.72)
 Stage 1 hypertension15 (0.4) (95% CI: 0.0020 to 0.0060)
GDM during current pregnancy (N=2962)424 (14.3) (95% CI: 0.13 to 0.16)
Anaemia (N=3097)1377 (44.5) (95% CI: 0.42 to 0.46)
Obstetrical characteristics (N=4778)
Gravida
 Primigravida1920 (40.2)
 Multigravida2858 (59.8)
Parity
 Nulliparous2178 (45.6)
 Multiparous2600 (54.4)
Mean Gestational age at delivery (week) (N=3324)38.70±3.02
Depressive symptoms and social support
 EPDS score at pregnancy (>13 cut-off) (N=4635)289 (6.2)
 Social support score above 24 (N=4643)1520 (32.7)
 EPDS score at delivery (>13 cut-off) (N=2801)471 (16.8)
Health status of mothers at delivery (N=3324)
 Healthy3054 (92.0)
 Morbidity/hospitalisation* Death259 (7.8)
7 (0.2)
Child characteristics n (%)
Health status at birth (N=3310)
 Healthy3188 (96.3)
 Morbidity/hospitalisation†49 (1.5)
 Death73 (2.2)
 Preterm deliveries (N=4862)430 (8.8)
Birth weight (N=4862)
 Underweight <2500 g384 (7.9)
 Normal 2500 g to 3500 g1625 (33.4)
 Overweight >3500 g2853 (58.7)
Birth weight according to Gestational Age (N=4862)
 Small for Gestational Age (SGA)159 (3.3)
 Mean±SD wt for SGA (kg)2.13±0.26
 Large for gestational age (LGA)523 (10.8)
 Mean±SD wt for LGA (kg)4.10±0.72
Delivery type (N=3324)
 Vaginal delivery1868 (56.2)
 Caesarean section1456 (43.8)
Sex (N=3309)
 Male1717 (51.9)
 Female1592 (48.1)
Baby cried soon after delivery (N=3310)3030 (91.5)
Colostrum fed to the baby (N=2915)2562 (87.9)
Breast milk fed as first food to the baby (N=2915)1932 (66.3)
Initiation of breast feeding after delivery (N=2890)
 Within an hour1227 (42.4)
 Between 1 and 24 hours1538 (53.2)
 After 24 hours125 (4.4)

GDM: Fasting blood sugar equal to or more than 92 mg/dL or 2-hour postprandial blood sugar equal to or more than 152 mg/dL. Hypertension: normal: SBP <120 mm Hg and DBP <80 mm Hg; prehypertension: SBP 120–139 mm Hg or DBP 80–89 mm Hg; stage 1 hypertension: SBP 140–159 mm Hg or DBP 90–99 mm Hg.

*Morbidity/hospitalisation (mother): postpartum haemorrhage, anaemia, infections, hypertensive disorder, diabetes mellitus, respiratory illness, thyroid disease.

†Morbidity/hospitalisation (newborn): fever, admission to NICU due to jaundice, low birth weight, IUGR, allergy, asphyxia, respiratory distress syndrome, Gastrointestinal abnormalities, congenital anomaly, macrocephaly, birth trauma, meconium aspiration, premature baby, infections, convulsions, pneumonia, hypoglycaemia.

DBP, diastolic blood pressure; EPDS, Edinburgh Postnatal Depression Scale; GDM, gestational diabetes mellitus; IUGR, Intrauterine growth restriction; MAASTHI, Maternal Antecedents of Adiposity and Studying the transgenerational role of Hyperglycaemia and Insulin; NICU, neonatal intensive care unit; PUC, Pre-university college; SBP, systolic blood pressure.

Baseline characteristics of eligible pregnant mothers and children in the MAASTHI birth cohort, Bengaluru, 2016–2021 GDM: Fasting blood sugar equal to or more than 92 mg/dL or 2-hour postprandial blood sugar equal to or more than 152 mg/dL. Hypertension: normal: SBP <120 mm Hg and DBP <80 mm Hg; prehypertension: SBP 120–139 mm Hg or DBP 80–89 mm Hg; stage 1 hypertension: SBP 140–159 mm Hg or DBP 90–99 mm Hg. *Morbidity/hospitalisation (mother): postpartum haemorrhage, anaemia, infections, hypertensive disorder, diabetes mellitus, respiratory illness, thyroid disease. †Morbidity/hospitalisation (newborn): fever, admission to NICU due to jaundice, low birth weight, IUGR, allergy, asphyxia, respiratory distress syndrome, Gastrointestinal abnormalities, congenital anomaly, macrocephaly, birth trauma, meconium aspiration, premature baby, infections, convulsions, pneumonia, hypoglycaemia. DBP, diastolic blood pressure; EPDS, Edinburgh Postnatal Depression Scale; GDM, gestational diabetes mellitus; IUGR, Intrauterine growth restriction; MAASTHI, Maternal Antecedents of Adiposity and Studying the transgenerational role of Hyperglycaemia and Insulin; NICU, neonatal intensive care unit; PUC, Pre-university college; SBP, systolic blood pressure. We found the prevalence of GDM in these women was 14.3% with 95% CI: 0.13 to 0.16 (n=424/2962). Among the recruited participants, 265 were prehypertensive (7.1%; 95% CI: 0.69% to 0.72%) and 15 were hypertensive (0.4%; 95% CI: 0.0020% to 0.0060%), while 44.5% of the women were anaemic (n=1377; 95% CI: 0.42 to 0.46). Using the cut-off value of 13 for EPDS, we found that 6.2% of women (n=289) had depressive symptoms indicative of depression during pregnancy and symptoms of postnatal depression were present in 16.8% of women (n=471). The mean gestational age at delivery was 38.7±3.02 weeks. More than half of the newborns were males (51.9%; n=1717), 43.8% of the infants were delivered by caesarean section (n=1456), and 91.2% infants were born full term (n=4432) (table 2). Table 3 summarises the anthropometric measurements of the participants (mothers) and their offspring during each phase of the study period respectively. Categorisation is based on tertiles −10th, 10– 90th and >90th percentiles. Each table includes mean and SD values for the measurements described in the analysis, and the frequency and proportion of mother and child in each tertile. We found that among the mothers above the 90th percentile for weight, 9.9% were obese at delivery and subsequent follow-ups. They weighed an average of 82.74 kg as compared with 83.84 kg at the 3 years follow-up. During the period from delivery to the 3-year follow-up, the average SFT in women with obesity (>90th percentile of SFT) changed from 76.6 mm (9.7%) to 75.46 mm (9.9%) in comparison to women with a normal range of SFT (10–90th percentile) in whom it changed from 46.54 mm (80.6%) to 49.79 mm (80.2%) (table 3).
Table 3

Anthropometry of the mother at different follow-up periods of the MAASTHI birth cohort, Bengaluru, 2016–2021

Anthropometric measurementDuring pregnancy (N=3734)14th week follow-up (N=2146)1-year follow-up (N=1255)2-year follow-up (N=801)3-year follow-up (N=393)
n (%)Mean (SD)n (%)Mean (SD)n (%)Mean (SD)n (%)Mean (SD)n (%)Mean (SD)
Weight<10 th percentile367 (9.8)41.88 (2.54)214 (10.0)40.35 (2.73)124 (9.9)38.96 (2.21)80 (10.0)40.25 (2.91)39 (9.9)40.41 (2.04)
10–90th percentile2996 (80.2)58.09 (7.60)1720 (80.1)56.90 (7.76)1006 (80.2)56.54 (8.00)642 (80.1)59.25 (8.18)315 (80.2)59.27 (8.31)
>90 th percentile371 (9.9)82.74 (7.07)212 (9.9)81.27 (6.56)124 (9.9)81.79 (7.02)79 (9.9)85.86 (8.51)39 (9.9)83.84 (7.07)
Waist circumference<10 th percentile194 (9.6)61.51 (3.71)124 (9.9)60.18 (2.97)80 (10.0)61.04 (2.71)38 (9.7)60.27 (3.65)
10–90th percentile1635 (80.8)77.96 (7.51)1006 (80.2)77.43 (7.61)641 (80.0)79.87 (8.41)319 (81.2)79.01 (8.06)
>90 th percentile195 (9.6)99.46 (6.23)125 (10)98.99 (6.15)80 (10.0)103.59 (6.00)36 (9.2)98.82 (4.07)
MUAC<10 th percentile358 (9.6)20.01 (1.15)190 (8.8)20.57 (1.02)124 (9.9)20.39 (1.19)74 (9.2)20.59 (1.44)39 (9.9)20.44 (1.41)
10–90th percentile3002 (80.4)25.78 (2.55)1744 (81.2)26.42 (2.52)1012 (80.6)26.74 (2.62)649 (81.0)27.65 (2.68)315 (80.2)27.30 (2.65)
>90 th percentile372 (10.0)33.54 (2.11)213 (9.9)34.03 (2.08)119 (9.5)43.43 (2.05)78 (9.7)35.30 (2.05)39 (9.9)34.44 (1.66)
Total SFT<10 th percentile361 (9.7)25.21 (2.91)213 (9.9)24.72 (3.51)124 (9.9)22.44 (3.38)79 (9.9)25.37 (4.19)39 (9.9)24.19 (4.12)
10–90th percentile3008 (80.6)46.54 (10.05)1723 (80.3)46.84 (9.59)1007 (80.2)45.93 (10.17)641 (80.1)50.69 (10.20)315 (80.2)49.79 (10.17)
>90 th percentile363 (9.7)76.60 (8.31)210 (9.8)73.83 (6.75)125 (10.0)73.92 (6.04)80 (10.0)79.55 (8.15)39 (9.9)75.46 (7.00)
Hip Circumference<10 th percentile199 (9.8)79.39 (4.85)121 (9.6)77.52 (4.00)80 (10.0)78.71 (5.93)39 (9.9)80.33 (3.29)
10–90th percentile1624 (80.2)94.99 (6.71)1013 (80.7)94.75 (7.06)642 (80.1)97.18 (7.16)315 (80.2)96.69 (6.89)
>90 th percentile201 (9.9)115.35 (5.47)121 (9.6)115.47 (5.71)79 (9.9)118.56 (5.75)39 (9.9)115.63 (3.29)
Height<10 th percentile368 (9.9)144.15 (2.27)
10–90th percentile2993 (80.2)153.81 (3.80)
>90 th percentile373 (10.0)164.16 (2.77)
Head circumference<10 th percentile329 (8.8)49.46 (1.09)
10–90th percentile3080 (82.5)52.69 (1.15)
>90 th percentile324 (8.7)56.08 (1.00)

MAASTHI, Maternal Antecedents of Adiposity and Studying the transgenerational role of Hyperglycaemia and Insulin; MUAC, mid-upper arm chest; SFT, skinfold thickness.

Anthropometry of the mother at different follow-up periods of the MAASTHI birth cohort, Bengaluru, 2016–2021 MAASTHI, Maternal Antecedents of Adiposity and Studying the transgenerational role of Hyperglycaemia and Insulin; MUAC, mid-upper arm chest; SFT, skinfold thickness. Anthropometric measurements of children showed that the sum of SFT ranged from 22.37 mm to 32.6 mm from birth to the 3-year follow-up for children above the 90th percentile compared with 13.76 mm to 22.87 mm, respectively, in children between 10 and 90th percentile. Birth of a high proportion of obese children (weight above 90th percentile), that is, 9.7%, was noted in our study (table 4). We also noted that 7.9% of children born were LBW (2500 g or less) and 8.8% (n=430) were born preterm. A high proportion of 10.8% (n=523) of children born were large for gestational age (LGA) in our cohort, and 3.3% were small for gestational age (SGA) (n=159). The mean weight of children who were SGA at birth was 2.13±0.26 kg and was 4.10±0.72 kg for children with LGA.
Table 4

Anthropometry of the child at different follow-up periods of the MAASTHI birth cohort, Bengaluru, 2016–2021

Anthropometric measurementAt birth14-week follow-up1-year follow-up2-year follow-up3-year follow-up
n (%)Mean (SD)n (%)Mean (SD)n (%)Mean (SD)n (%)Mean (SD)n (%)Mean (SD)
Weight<10 th percentile243 (9.8)2.14 (0.21)182 (8.5)4.31 (0.39)122 (9.7)6.84 (0.38)74 (9.0)8.56 (0.62)41 (10.0)9.80 (0.64)
10–90th percentile2003 (80.5)2.98 (0.41)1761 (82.4)6.04 (0.72)1010 (80.5)8.74 (0.82)670 (81.5)10.73 (0.90)333 (81.2)12.30 (0.95)
>90 th percentile242 (9.7)4.78 (0.74)195 (9.1)8.37 (0.73)122 (9.7)11.43 (0.85)78 (9.5)13.41 (0.77)36 (8.8)14.74 (0.28)
CRL<10 th percentile233 (9.4)27.37 (2.01)213 (10.0)33.21 (1.89)114 (9.9)37.28 (2.48)
10–90th percentile2020 (81.5)32.41 (2.01)1719 (80.6)40.52 (2.40)926 (80.2)45.31 (2.36)
>90 th percentile226 (9.1)39.29 (2.21)202 (9.5)47.66 (2.79)114 (9.9)53.44 (4.00)
Length<10 th percentile248 (10.0)43.69 (1.72)206 (9.6)55.26 (2.22)125 (10.0)65.76 (6.28)79 (9.6)74.64 (3.09)41 (10.0)83.16 (3.42)
10–90th percentile2009 (80.8)49.38 (2.28)1720 (80.5)62.66 (2.74)1003 (80.2)73.79 (2.65)664 (80.8)83.17 (2.92)329 (80.2)90.78 (2.77)
>90 th percentile230 (9.2)58.06 (2.81)211 (9.9)70.99 (2.24)123 (9.8)81.68 (2.78)79 (9.6)91.61 (2.23)40 (9.8)97.89 (1.65)
Head circumference<10 th percentile242 (9.7)30.30 (1.07)199 (9.3)36.30 (2.05)102 (8.1)40.39 (1.79)81 (9.9)42.49 (1.45)39 (9.5)43.96 (0.87)
10–90th percentile2001 (80.4)33.66 (1.33)1740 (81.4)40.07 (1.33)1033 (82.4)44.23 (1.16)666 (81.3)46.16 (1.25)332 (81.0)47.10 (1.09)
>90 th percentile245 (9.8)38.10 (1.25)199 (9.3)43.97 (0.96)119 (9.5)47.41 (1.33)72 (8.8)50.81 (4.86)39 (9.5)50.27 (1.48)
Chest circumference<10 th percentile246 (9.9)28.10 (1.19)198 (9.3)35.67 (1.02)125 (10.0)39.73 (1.89)69 (8.4)42.54 (1.41)38 (9.3)44.57 (0.87)
10–90 percentile2014 (80.9)32.24 (1.73)1740 (81.4)40.12 (1.71)1017 (81.1)44.35 (1.58)673 (81.8)46.78 (1.58)333 (81.2)48.56 (1.69)
>90 th percentile228 (9.2)38.38 (1.83)200 (9.4)45.08 (1.27)112 (8.9)49.15 (1.48)81 (9.8)56.49 (1.64)39 (9.5)53.0 (1.04)
Waist circumference<10 th percentile235 (9.4)24.81 (1.17)182 (8.5)33.14 (1.46)2 (0.2)29.30 (1.69)77 (9.3)40.17 (1.64)41 (10.0)41.93 (1.20)
10–90 percentile2008 (80.7)30.66 (2.47)1747 (81.7)39.28 (2.29)1132 (90.3)41.95 (2.86)667 (80.9)45.57 (1.98)329 (80.2)46.94 (2.09)
>90 th percentile245 (9.8)38.24 (1.87)209 (9.8)45.37 (1.58)119 (9.5)49.02 (1.83)80 (9.7)51.39 (1.96)40 (9.8)53.27 (1.40)
Hip circumference<10 th percentile211 (8.5)23.67 (0.93)211 (9.9)32.05 (1.49)4 (0.3)30.75 (2.12)79 (9.6)39.71 (1.47)39 (9.5)41.70 (4.69)
10–90 percentile2037 (81.9)28.91 (2.44)1717 (80.3)39.05 (2.85)1125 (89.7)42.17 (3.06)669 (81.2)46.23 (2.51)332 (81.0)48.71 (2.50)
>90 th percentile240 (9.6)37.32 (2.68)210 (9.8)46.42 (1.60)125 (10.0)50.0 (1.97)76 (9.2)53.47 (1.87)39 (9.5)55.21 (1.31)
MUAC<10 th percentile191 (7.7)7.86 (0.58)206 (9.6)10.58 (0.76)124 (9.9)11.25 (0.96)78 (9.5)11.65 (0.82)39 (9.5)12.28 (1.47)
10–90 percentile2074 (83.4)9.81 (0.76)1748 (81.8)12.88 (0.82)1015 (80.9)13.77 (0.84)665 (80.8)14.15 (0.80)333 (81.2)14.57 (0.73)
>90 th percentile223 (9.0)12.48 (0.77)183 (8.6)15.31 (0.70)115 (9.2)16.25 (1.52)80 (9.7)16.72 (1.03)38 (9.3)17.76 (5.78)
Total SFT<10 th percentile223 (9.0)9.27 (0.78)196 (9.2)14.25 (1.20)119 (9.5)14.36 (0.98)78 (9.5)14.94 (1.20)40 (9.8)15.53 (1.06)
10–90 percentile2005 (81.0)13.76 (2.14)1723 (81.2)20.80 (2.61)1006 (80.5)19.98 (2.47)670 (81.4)21.58 (3.05)332 (81.0)22.87 (3.41)
>90 th percentile246 (9.9)22.37 (3.25)204 (9.6)29.45 (3.31)124 (9.9)28.02 (2.74)75 (9.1)32.46 (3.74)38 (9.3)32.60 (3.28)

MAASTHI, Maternal Antecedents of Adiposity and Studying the transgenerational role of Hyperglycaemia and Insulin; MUAC, mid-upper arm chest; SFT, skinfold thickness.

Anthropometry of the child at different follow-up periods of the MAASTHI birth cohort, Bengaluru, 2016–2021 MAASTHI, Maternal Antecedents of Adiposity and Studying the transgenerational role of Hyperglycaemia and Insulin; MUAC, mid-upper arm chest; SFT, skinfold thickness.

Strengths and limitations

As there is no unanimity regarding appropriate guidelines for diagnosing GDM in the Indian population, our findings can provide specific evidence regarding exact cut-off points to be used for the diagnosis. The high prevalence of GDM may provide evidence for a policy decision to scale up screening and management of GDM in all the public health facilities. Above this it may be associated with adverse maternal and childhood outcomes. Also, the huge burden of depressive symptoms among mothers, draws attention to the importance of mental health screening as part of routine antenatal care. We found a high number of children born LGA. In addition, the prevalence of obesity at birth and subsequent follow-ups was also high (above 9%). If unchanged modifiable factors of obesity such as diet, exercise and GDM, will continue the vicious cycle of afflicting subsequent generations.41 The results from our cohort will continue to inform and shape policies regarding screening, appropriate care and management for persons affected with GDM, perinatal depression and childhood obesity. MAASTHI is a well-established cohort study documenting the life course trajectory in the genesis of non-communicable diseases (NCDs). We are documenting important exposure contrasts experienced by women early in their pregnancy and continue to document the outcomes across the process of pregnancy, childbirth and early childhood, including assessing important milestones of the child. In India, public health facilities are the preferred choice for many women42 from the lower social strata. Our findings revealed an unusually high burden of GDM and maternal obesity similar to earlier studies43–46 for women between the age group of 18–45 years. Our cohort study will inform policies in achieving further reductions in maternal and fetal mortality and morbidity. For example, achieving the desired level of glycaemic control during pregnancy can reduce several maternal and fetal adverse effects.47 Early screening and timely management of GDM may prevent some poor outcomes for mother and child. The strength of MAASTHI is that data pertain to the pregnant women and children belonging to lower-income and middle-income socioeconomic status-seeking healthcare from the public health facilities with a strong representation of minority groups and vulnerable sections of the society. Also, this is probably the only pregnancy cohort recruited from public health facilities in India. Although the acronym suggests the transgenerational role of glucose and insulin, the study was conceptualised to include important maternal determinants of underweight and childhood obesity. The comprehensive exposure assessments in MAASTHI include the role of nutritional, psychosocial, and, recently more relevant—air pollution throughout pregnancy and different time points of the life course.48 Attention to obtaining high-quality data by maintaining stringent quality checks for reproducible measurements and minimal errors is another major strength of this study. Moreover, blood aliquots are stored in the biorepository for future studies on childhood obesity. Operational issues in terms of incomplete OGTT and lost to follow-up after delivery are the limitations of conducting a study in public health facilities. Without a registry or defined population for healthcare services, this limitation will continue to affect implementing cohort studies in public health facilities. Periods of prolonged fasting (previous night) coupled with the issue of gastritis/morning sickness in pregnant women are other factors responsible for incomplete OGTT. As with most research during COVID-19, our cohort was also subject to data collection issues. Our research staff had to resolve the inability of physical contact for face-to-face interviews through telephonic interviews. However, no physical meetings meant the complete stop to anthropometric measurements for mother–child dyads. By setting up and following up this cohort, we can inform the design and implement interventions focusing on health promotion and disease prevention, address undernutrition and overweight epidemics, and thereby contribute to reducing the NCD disease profile in the country.
  38 in total

1.  Diabetes mellitus: a "thrifty" genotype rendered detrimental by "progress"?

Authors:  J V NEEL
Journal:  Am J Hum Genet       Date:  1962-12       Impact factor: 11.025

Review 2.  The thrifty phenotype hypothesis.

Authors:  C N Hales; D J Barker
Journal:  Br Med Bull       Date:  2001       Impact factor: 4.291

3.  Fuel-mediated teratogenesis. Use of D-mannose to modify organogenesis in the rat embryo in vivo.

Authors:  T Buchanan; N Freinkel; N J Lewis; B E Metzger; S Akazawa
Journal:  J Clin Invest       Date:  1985-06       Impact factor: 14.808

4.  Size at birth, maternal weight, and type 2 diabetes in South India.

Authors:  C H Fall; C E Stein; K Kumaran; V Cox; C Osmond; D J Barker; C N Hales
Journal:  Diabet Med       Date:  1998-03       Impact factor: 4.359

Review 5.  Maternal depression and infant growth: a review of recent evidence.

Authors:  Robert C Stewart
Journal:  Matern Child Nutr       Date:  2007-04       Impact factor: 3.092

6.  IDF Diabetes Atlas: Global estimates for the prevalence of diabetes for 2015 and 2040.

Authors:  K Ogurtsova; J D da Rocha Fernandes; Y Huang; U Linnenkamp; L Guariguata; N H Cho; D Cavan; J E Shaw; L E Makaroff
Journal:  Diabetes Res Clin Pract       Date:  2017-03-31       Impact factor: 5.602

7.  Prevalence and associated risk factors for gestational diabetes in Jos, North-central, Nigeria.

Authors:  Ajen Stephen Anzaku; Jonah Musa
Journal:  Arch Gynecol Obstet       Date:  2012-12-06       Impact factor: 2.344

8.  Gestational diabetes in India: Science and society.

Authors:  Ambrish Mithal; Beena Bansal; Sanjay Kalra
Journal:  Indian J Endocrinol Metab       Date:  2015 Nov-Dec

9.  Antenatal depression and its association with adverse birth outcomes in low and middle-income countries: A systematic review and meta-analysis.

Authors:  Abel Fekadu Dadi; Emma R Miller; Lillian Mwanri
Journal:  PLoS One       Date:  2020-01-10       Impact factor: 3.240

10.  What makes the pregnant women revisit public hospitals for research? Participant engagement and retention trial in a public hospital (PERTH): an RCT protocol.

Authors:  Giridhara R Babu; Maithili Karthik; Deepa Ravi; Yamuna Ana; Prafulla Shriyan; Kiran Kumar Hasige; Keerti Deshpande; Lokesh Bangalore Siddlingaiah; Sanjay Kinra; Gudlavalleti Venkata Satyanarayana Murthy
Journal:  BMC Pregnancy Childbirth       Date:  2018-09-12       Impact factor: 3.007

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