TY - JOUR
T1 - Impact of preterm birth on brain development and long-term outcome
T2 - protocol for a cohort study in Scotland
AU - Boardman, James P
AU - Hall, Jill
AU - Thrippleton, Michael J
AU - Reynolds, Rebecca M
AU - Bogaert, Debby
AU - Davidson, Donald J
AU - Schwarze, Jurgen
AU - Drake, Amanda J
AU - Chandran, Siddharthan
AU - Bastin, Mark E
AU - Fletcher-Watson, Sue
N1 - Funding Information:
Funding The Theirworld Edinburgh Birth Cohort study is funded by the charity Theirworld (www.theirworld.org) and is carried out in the University of Edinburgh MRC Centre for Reproductive Health (MRC G1002033). Susceptibility to viral infection studies is supported by grants from Action Medical Research (GN2703) and Chief Scientist Office (TCS/18/02). Respiratory microbiota studies are supported by grants from the Chief Scientist Office (SCAF/16/03), and DNA methylation and gut microbiota studies are supported by the Wellcome Trust (203769/Z/16/A and 220043/Z/19/Z). The MRI facility is funded by Wellcome Trust (104916/Z/14/Z), Dunhill Trust (R380R/1114), Edinburgh and Lothians Health Foundation (2012/17), Muir Maxwell Research Fund and Edinburgh Imaging, University of Edinburgh. MJT was supported by NHS Lothian Research and Development Office, and RMR and AJD received support from the British Heart Foundation (RE/18/5/34216).
Publisher Copyright:
© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/3/4
Y1 - 2020/3/4
N2 - INTRODUCTION: Preterm birth is closely associated with altered brain development and is a leading cause of neurodevelopmental, cognitive and behavioural impairments across the life course. We aimed to investigate neuroanatomic variation and adverse outcomes associated with preterm birth by studying a cohort of preterm infants and controls born at term using brain MRI linked to biosamples and clinical, environmental and neuropsychological data.METHODS AND ANALYSIS: Theirworld Edinburgh Birth Cohort is a prospective longitudinal cohort study at the University of Edinburgh. We plan to recruit 300 infants born at <33 weeks of gestational age (GA) and 100 healthy control infants born after 37 weeks of GA. Multiple domains are assessed: maternal and infant clinical and demographic information; placental histology; immunoregulatory and trophic proteins in umbilical cord and neonatal blood; brain macrostructure and microstructure from structural and diffusion MRI (dMRI); DNA methylation; hypothalamic-pituitary-adrenal axis activity; social cognition, attention and processing speed from eye tracking during infancy and childhood; neurodevelopment; gut and respiratory microbiota; susceptibility to viral infections; and participant experience. Main analyses include creation of novel methods for extracting information from neonatal structural and dMRI, regression analyses of predictors of brain maldevelopment and neurocognitive outcome associated with preterm birth, and determination of the quantitative predictive performance of MRI and other early life factors for childhood outcome.ETHICS AND DISSEMINATION: Ethical approval has been obtained from the National Research Ethics Service (NRES), South East Scotland Research Ethics Committee (NRES numbers 11/55/0061 and 13/SS/0143 (phase I) and 16/SS/0154 (phase II)), and NHS Lothian Research and Development (2016/0255). Results are disseminated through open access journals, scientific meetings, social media, newsletters anda study website (www.tebc.ed.ac.uk), and we engage with the University of Edinburgh public relations and media office to ensure maximum publicity and benefit.
AB - INTRODUCTION: Preterm birth is closely associated with altered brain development and is a leading cause of neurodevelopmental, cognitive and behavioural impairments across the life course. We aimed to investigate neuroanatomic variation and adverse outcomes associated with preterm birth by studying a cohort of preterm infants and controls born at term using brain MRI linked to biosamples and clinical, environmental and neuropsychological data.METHODS AND ANALYSIS: Theirworld Edinburgh Birth Cohort is a prospective longitudinal cohort study at the University of Edinburgh. We plan to recruit 300 infants born at <33 weeks of gestational age (GA) and 100 healthy control infants born after 37 weeks of GA. Multiple domains are assessed: maternal and infant clinical and demographic information; placental histology; immunoregulatory and trophic proteins in umbilical cord and neonatal blood; brain macrostructure and microstructure from structural and diffusion MRI (dMRI); DNA methylation; hypothalamic-pituitary-adrenal axis activity; social cognition, attention and processing speed from eye tracking during infancy and childhood; neurodevelopment; gut and respiratory microbiota; susceptibility to viral infections; and participant experience. Main analyses include creation of novel methods for extracting information from neonatal structural and dMRI, regression analyses of predictors of brain maldevelopment and neurocognitive outcome associated with preterm birth, and determination of the quantitative predictive performance of MRI and other early life factors for childhood outcome.ETHICS AND DISSEMINATION: Ethical approval has been obtained from the National Research Ethics Service (NRES), South East Scotland Research Ethics Committee (NRES numbers 11/55/0061 and 13/SS/0143 (phase I) and 16/SS/0154 (phase II)), and NHS Lothian Research and Development (2016/0255). Results are disseminated through open access journals, scientific meetings, social media, newsletters anda study website (www.tebc.ed.ac.uk), and we engage with the University of Edinburgh public relations and media office to ensure maximum publicity and benefit.
KW - MRI
KW - child & adolescent psychiatry
KW - developmental neurology & neurodisability
KW - maternal medicine
KW - neonatal intensive & critical care
KW - paediatric neurology
UR - http://www.scopus.com/inward/record.url?scp=85081272712&partnerID=8YFLogxK
U2 - 10.1136/bmjopen-2019-035854
DO - 10.1136/bmjopen-2019-035854
M3 - Article
C2 - 32139495
SN - 2044-6055
VL - 10
SP - 1
EP - 11
JO - BMJ Open
JF - BMJ Open
IS - 3
M1 - e035854
ER -