Singapore PREconception Study of Long-Term Maternal and Child Outcomes

Sponsor
KK Women's and Children's Hospital (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03531658
Collaborator
National University Health System, Singapore (Other), Singapore Institute for Clinical Sciences (Other)
1,054
1

Study Details

Study Description

Brief Summary

The study aims to evaluate how preconception and early prenatal environmental factors can potentially influence health outcomes for both mother and child during pregnancy and postnatally.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    It is now evident that prenatal stage represents a window of susceptibility for early life exposure that can have an effect on developing fetus, with potential long-lasting consequences for offspring growth and development. Emerging research suggest that the environmental modulation of tissue development and function may even occur both before and soon after conception but as yet, limited study has been conducted to investigate the relationship of preconception and early prenatal life conditions, including nutrition, lifestyle and environmental factors, with maternal and offspring health.

    This prospective preconception cohort study recruited 1054 women who plan to get pregnant. The investigators will assess the women metabolically, nutritionally and epigenetically, then monitor them from their first missed menses with nutritional surveys and assays and repeated bio-sampling to birth followed by assessment in the women of lactation and lactational nutrition. Biochemical and molecular analyses will be done on the cord and placenta at birth and in buccal smears at frequent postnatal intervals. The women's partners will also be recruited on consent. Phenotypic measures of body composition and core neurodevelopmental measures will be followed in the offspring from birth until 7 years of age. Metabolic and mental health of women will also be measured from preconception until 7 years postpartum. At delivery phase, there are 373 mother-child pairs with 80% of fathers enrolled in the study as well.

    This study allows understanding of the potential triggers during early life environment, including nutritional and lifestyle factors, emotional wellbeing, socio-economic status, microbiome, pollutants, metabolomics and epigenetics, which can independently or collectively influence metabolic and neural phenotypes in the offspring and mother. This will help to establish what future directions may hold in terms of possible preventive strategies that may lead to decreased prevalence of metabolic diseases and mental/ neurological disorders.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    1054 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Singapore PREconception Study of Long-Term Maternal and Child Outcomes (S-PRESTO)
    Actual Study Start Date :
    Feb 27, 2015
    Anticipated Primary Completion Date :
    Jul 1, 2026

    Outcome Measures

    Primary Outcome Measures

    1. Offspring adiposity [Up to 84 months, from birth until 7 years of age]

      Offspring adiposity (total and percentage fat mass) measured by skinfold calipers, air-displacement plethysmography, quantitative magnetic resonance (QMR) and Magnetic resonance imaging (MRI).

    2. Offspring neurocognitive and behavioural development [Up to 9 months, from 3-12 months of age]

      Offspring neurocognitive and behavioural development measured by questionnaires, behavioural tasks and brain MRI.

    Secondary Outcome Measures

    1. Duration of gestation [Up to 42 weeks, between estimated date of conception based on ultrasound scan and date of delivery]

    2. Fetal growth measured by ultrasound scan [Up to 30 weeks, between 6-36 weeks of gestation]

    3. Offspring body weight measured by calibrated weighing scale [Up to 84 months, from birth until 7 years of age]

    4. Offspring growth trajectories [Up to 84 months, from birth until 7 years of age]

    5. Offspring adiposity trajectories (total and percentage fat mass) [Up to 84 months, from birth until 7 years of age]

    6. Offspring anogenital distance measured by Vernier calipers [Up to 12 months, from birth until 12 months of age]

    7. Offspring allergic wellbeing measured by skin examination and skin prick test [Up to 84 months, from 1 week until 7 years of age]

    8. Offspring skin microbiome collected by sterile tape strips [Up to 84 months, from 1 week until 7 years of age]

    9. Offspring metabolomics, lipidomics and pollutant profile measured through biospecimens such as cord, cord blood, heel prick blood, and hair samples [Up to 24 months, from birth until 24 months of age]

    10. Offspring epigenetic profile measured through cord, cord blood, and buccal smear samples [Up to 84 months, from birth until 7 years of age]

    11. Offspring gut microbiome measured through stool samples [Up to 84 months, from birth until 7 years of age]

    12. Maternal glucose tolerance status measured by Oral Glucose Tolerance Test (OGTT) [At preconception, 27-28 weeks of gestation, 3 months postpartum and 24, 36, 48 months postpartum]

    13. Maternal weight measured by calibrated weighing scale [Up to 106 months, between preconception, pregnancy and 7 years postpartum]

    14. Changes in maternal weight before, during and after gestation [Up to 106 months, between preconception, pregnancy and 7 years postpartum]

    15. Maternal body weight status determined by body mass index based on weight (kg) /height (m)2 [At preconception visit; 3-84 months postpartum]

    16. Maternal body composition measured by skinfold calipers, air-displacement plethysmography, bioelectrical impedance analysis and dual-energy X-ray absorptiometry (DXA) [Up to 106 months, between preconception, pregnancy (only using skinfold caliper) and 7 years postpartum]

    17. Changes in maternal body composition before, during and after gestation [Up to 106 months, between preconception, pregnancy and 7 years postpartum]

    18. Maternal cardiovascular health (subsample) measured through clinical examination [At preconception, 27-28 weeks of gestation, 6 months postpartum]

    19. Maternal blood pressure measured by semi-automatic blood pressure device [Up to 106 months, between preconception, pregnancy and 7 years postpartum]

    20. Maternal allergic wellbeing measured by questionnaires and skin prick test [Up to 40 months, between preconception, pregnancy and 18 months postpartum]

    21. Maternal skin microbiome collected by sterile tape strips [34-36 weeks of gestation and 18 months postpartum]

    22. Maternal emotional wellbeing measured by Edinburgh Post-natal Depression Scale and State-Trait Anxiety Inventory [Up to 70 months, between preconception, pregnancy and 48 months postpartum]

    23. Maternal mental health measured by questionnaires and behavioural tasks [Up to 46 months, between preconception, pregnancy and 24 months postpartum]

    24. Mode of delivery [Delivery]

    25. Pregnancy complications obtained from questionnaires and clinical documents [Up to 41 weeks, between early pregnancy and delivery]

    26. Time to pregnancy [Up to 12 months, between the date of last menstrual period obtained from the first preconception visit and before conception (if pregnant) or the most recent follow up (if not pregnant)]

    27. Pregnancy and live birth rates based on ultrasound scan [Between early pregnancy and delivery]

    28. Maternal metabolomics, lipidomics and pollutant profile measured from biospecimens such as blood, urine, hair [Up to 106 months, from preconception (up to 12 months) to pregnancy (10 months) and up to 7 years postpartum]

    29. Maternal epigenetic profile measured from blood and buccal smear samples [Up to 106 months, from preconception (up to 12 months) to pregnancy (10 months) and up to 7 years postpartum]

    30. Maternal transcription profile measured from blood samples [Up to 106 months, from preconception (up to 12 months) to pregnancy (10 months) and up to 7 years postpartum]

    31. Maternal, paternal and offspring genotyping (blood or buccal samples) [Up to 106 months, from preconception (up to 12 months) to pregnancy (10 months) and up to 7 years postpartum]

    32. Maternal micronutrient status measured from blood samples [Up to 106 months, from preconception (up to 12 months) to pregnancy (10 months) and up to 7 years postpartum]

    33. Maternal microbiota composition profile measured from stool and epithelial (breast, vaginal and rectal) swab samples [Up to 24 months, preconception, to pregnancy, pre-delivery and 6 weeks postpartum]

    34. Breast milk macronutrient profile [Up to 6 months, from 1 week to 6 months postpartum]

    35. Breast milk micronutrient profile [Up to 6 months, from 1 week to 6 months postpartum]

    36. Breast milk metabolomic profile [Up to 6 months, from 1 week to 6 months postpartum]

    37. Breast milk epigenetic profile [Up to 6 months, from 1 week to 6 months postpartum]

    38. Maternal and infant transcriptomics (including of breast milk) [Up to 28 months, between preconception, pregnancy and 6 months postpartum]

    39. Influence of parental and offspring genotypes, body compositions, lifestyle and diet on the above primary and secondary outcomes [Up to 106 months, between preconception, pregnancy and 7 years postpartum]

    Other Outcome Measures

    1. Offspring health obtained from questionnaires and clinical documents [Up to 84 months, from birth until 7 years of age]

    2. Maternal health obtained from questionnaires and clinical documents [Up to 106 months, between preconception, pregnancy and 7 years postpartum]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 35 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    1. Women aged 18-35 years

    2. Intention to reside in Singapore for the next 5 years

    3. Chinese, Malay, Indian or any combinations of these 3 ethnic groups

    4. Planning to conceive within 1 year

    5. Able to provide written, informed consent

    Exclusion Criteria:
    1. Have been actively trying to conceive for more than 18 months

    2. Currently pregnant

    3. Assisted fertility, apart from those taking clomiphene alone in the past 1 month

    4. Established pre-existing diabetes (type 1 or type 2)

    5. Oral or implanted contraception, or with an IUCD in situ in the past 1 month

    6. On systemic steroids in the past 1 month

    7. On anticonvulsants in the past 1 month

    8. On HIV or Hepatitis B or C medication in the past 1 month

    9. Not becoming pregnant after more than 12 months from recruitment

    10. Eventual multiple pregnancies

    11. Pregnancy complications such as miscarriages, ectopic pregnancy, still birth

    The partners of the women will also be invited to participate in the study. Upon informed consent, fathers will have blood, urine, hair sampling, buccal swabs, body measurements and cognitive assessment. These will be done along with health and lifestyle questionnaire within one to two study visits.

    The mothers will consent for their children to have body measurements, cognitive assessment, buccal, hair, stool samples and allergy testing from birth to 7 years of age. Assent will also be taken when the child turns 6.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 KK Women's and Children's Hospital Singapore Singapore

    Sponsors and Collaborators

    • KK Women's and Children's Hospital
    • National University Health System, Singapore
    • Singapore Institute for Clinical Sciences

    Investigators

    • Principal Investigator: Jerry Kok Yen Chan, KK Women's and Children's Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    KK Women's and Children's Hospital
    ClinicalTrials.gov Identifier:
    NCT03531658
    Other Study ID Numbers:
    • 2014/692/D
    First Posted:
    May 22, 2018
    Last Update Posted:
    Apr 2, 2021
    Last Verified:
    Mar 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 2, 2021