Preterm birth as a determinant of neurodevelopment and cognition in children (PRENCOG): protocol for an exposure-based cohort study in the UK

• Published in: BMJ open 2024-09, Vol.14 (9), p.e085365
• Main Authors: Boardman, James P, Andrew, Ruth, Bastin, Mark E, Battersby, Cheryl, Batty, G David, Cábez, Manuel Blesa, Cox, Simon R, Hall, Jill, Ingledow, Lauren, Marioni, Riccardo E, Modi, Neena, Murphy, Lee, Quigley, Alan J, Reynolds, Rebecca M, Richardson, Hilary, Stock, Sarah J, Thrippleton, Michael J, Tsanas, Athanasios, Whalley, Heather C
• Format: Article
• Language: English
• Subjects: Adaptation; Biomarkers; Birth weight; Child Development; Children & youth; Cognition; Cognition & reasoning; Cohort analysis; Cohort Studies; Developmental neurology & neurodisability; DNA methylation; Epigenetics; Female; Gestational Age; Hormones; Humans; Immunity; Infant; Infant, Newborn; Infant, Premature; Inflammation; Intensive care; Machine Learning; Magnetic Resonance Imaging; Male; Metabolism; Neonatal intensive & critical care; Neurodevelopmental Disorders - etiology; Newborn babies; Paediatrics; Physiological Stress; Pregnancy; Premature babies; Premature Birth; Protocol; Research Design; Risk Factors; Socioeconomic factors; United Kingdom
• ISSN: 2044-6055; 2044-6055
• DOI: 10.1136/bmjopen-2024-085365

IntroductionPreterm birth (PTB) is strongly associated with encephalopathy of prematurity (EoP) and neurocognitive impairment. The biological axes linking PTB with atypical brain development are uncertain. We aim to elucidate the roles of neuroendocrine stress activation and immune dysregulation in linking PTB with EoP.Methods and analysisPRENCOG (PREterm birth as a determinant of Neurodevelopment and COGnition in children: mechanisms and causal evidence) is an exposure-based cohort study at the University of Edinburgh. Three hundred mother–infant dyads comprising 200 preterm births (gestational age, GA 37 weeks, non-exposed), will be recruited between January 2023 and December 2027. We will collect parental and infant medical, demographic, socioeconomic characteristics and biological data which include placental tissue, umbilical cord blood, maternal and infant hair, infant saliva, infant dried blood spots, faecal material, and structural and diffusion MRI. Infant biosamples will be collected between birth and 44 weeks GA.EoP will be characterised by MRI using morphometric similarity networks (MSNs), hierarchical complexity (HC) and magnetisation transfer saturation imaging (MTsat). We will conduct: first, multivariable regressions and statistical association assessments to test how PTB-associated risk factors (PTB-RFs) relate to MSNs, HC and or MTsat; second, structural equation modelling to investigate neuroendocrine stress activation and immune dysregulation as mediators of PTB-RFs on features of EoP. PTB-RF selection will be informed by the variables that predict real-world educational outcomes, ascertained by linking the UK National Neonatal Research Database with the National Pupil Database.Ethics and disseminationA favourable ethical opinion has been given by the South East Scotland Research Ethics Committee 02 (23/SS/0067) and NHS Lothian Research and Development (2023/0150). Results will be reported to the Medical Research Council, in scientific media, via stakeholder partners and on a website in accessible language (https://www.ed.ac.uk/centre-reproductive-health/prencog).