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早产作为儿童神经发育和认知的决定因素(PRENCOG):英国一项基于暴露的队列研究方案

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

作者信息

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

机构信息

Centre for Reproductive Health, University of Edinburgh, Edinburgh, UK

Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.

出版信息

BMJ Open. 2024 Sep 16;14(9):e085365. doi: 10.1136/bmjopen-2024-085365.

Abstract

INTRODUCTION

Preterm 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 ANALYSIS

PRENCOG (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 <32 weeks, exposed) and 100 term births (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 DISSEMINATION

A 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).

摘要

引言

早产(PTB)与早产儿脑病(EoP)及神经认知障碍密切相关。将早产与非典型脑发育联系起来的生物学轴尚不确定。我们旨在阐明神经内分泌应激激活和免疫失调在早产与早产儿脑病之间的联系中所起的作用。

方法与分析

PRENCOG(早产作为儿童神经发育和认知的决定因素:机制与因果证据)是爱丁堡大学开展的一项基于暴露的队列研究。2023年1月至2027年12月期间,将招募300对母婴,其中包括200例早产(胎龄,GA<32周,暴露组)和100例足月产(GA>37周,非暴露组)。我们将收集父母及婴儿的医疗、人口统计学、社会经济特征和生物学数据,包括胎盘组织、脐带血、母婴毛发、婴儿唾液、婴儿干血斑、粪便样本以及结构和弥散磁共振成像。婴儿生物样本将在出生至胎龄44周期间采集。将使用形态相似性网络(MSN)、层次复杂性(HC)和磁化传递饱和成像(MTsat)通过磁共振成像对早产儿脑病进行特征描述。我们将进行:第一,多变量回归和统计关联评估,以测试与早产相关的危险因素(PTB-RF)如何与MSN、HC和/或MTsat相关;第二,结构方程模型,以研究神经内分泌应激激活和免疫失调作为PTB-RF对早产儿脑病特征的介导因素。PTB-RF的选择将参考预测现实世界教育结果的变量,这些变量通过将英国国家新生儿研究数据库与国家学生数据库相链接来确定。

伦理与传播

苏格兰东南部研究伦理委员会02(23/SS/0067)和NHS洛锡安研究与发展部(2023/0150)已给出有利的伦理意见。研究结果将通过利益相关者合作伙伴,以通俗易懂的语言在科学媒体上以及网站(https://www.ed.ac.uk/centre-reproductive-health/prencog)上向医学研究理事会报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62bf/11409314/e2a721e251a3/bmjopen-14-9-g001.jpg

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