Inflammation and congenital heart disease

  • Research type

    Research Study

  • Full title

    Harnessing the maternal immune system to predict fetal congenital heart disease

  • IRAS ID

    345102

  • Contact name

    Suchita Nadkarni

  • Contact email

    s.nadkarni@qmul.ac.uk

  • Sponsor organisation

    Queen Mary University of London

  • Duration of Study in the UK

    2 years, 0 months, 0 days

  • Research summary

    Congenital heart disease (CHD) is the most common type of birth defect, affecting 1% of all pregnancies1. Despite the very early developmental stages of cardiac formation, with some cases of CHD detected at initial maternity booking scan (11-14weeks), the diagnosis of most CHDs does not occur until the 2nd trimester, between 18 and 22 weeks.
    Based on our previously published data, we hypothesise that the maternal immune system plays a pivotal role in the development of the fetal heart. Specifically, underlying maternal inflammation early in pregnancy negatively impacts placental development, which in turn leads to congenital heart anomalies in the developing fetus. Thus, indications of maternal inflammation in the first trimester of pregnancy could pave the way for biomarkers for the early prediction of fetal congenital heart diseases (CHD) and identify potential therapeutic targets and non-invasive interventions. To address our hypothesis, we will undertake 2 main aims:

    1. A retrospective cohort study to identify inflammatory markers in the maternal circulation within the first trimester of pregnancy from a cohort of confirmed fetal CHD cases and healthy controls, utilising stored Booking Blood samples taken at 10 weeks of pregnancy.
    2. An observational cohort study to analyse the immune cell status from maternal blood samples at the 20 week scan, when a fetal CHD has been confirmed and analyse placental tissue at time of delivery for inflammatory and structural changes

  • REC name

    West Midlands - Coventry & Warwickshire Research Ethics Committee

  • REC reference

    24/WM/0201

  • Date of REC Opinion

    18 Sep 2024

  • REC opinion

    Further Information Favourable Opinion