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Newcastle 1000 (NEW1000) Study: an Australian population-based prospective pregnancy cohort study design and protocol

Authors :
Simon Keely
John Attia
Andrew Boyle
Sarah R Valkenborghs
Roger Smith
Clare Collins
Penny Reeves
John Wiggers
Joerg Mattes
Andrew Searles
Frances Kay-Lambkin
Linda Campbell
Vanessa E Murphy
Peter Gibson
Craig Gedye
Tegan Grace
Rodney Scott
Kirsty Pringle
Maralyn Foureur
Craig E Pennell
Vanessa McDonald
Joshua Fisher
Carol Wang
Jonathan J Hirst
Craig Pennell
Mike Calford
Vanessa Murphy
Tracey Dudding-Bythe
Nick Talley
Emily Hoedt
Jay Horvat
Mitch Duncan
Sarah Valkenborghs
Emily Freeman
Source :
BMJ Open, Vol 13, Iss 7 (2023)
Publication Year :
2023
Publisher :
BMJ Publishing Group, 2023.

Abstract

Introduction Multiple cohort studies have been established to investigate the impact of early life factors on development and health outcomes. In Australia the majority of these studies were established more than 20 years ago and, although longitudinal in nature, are inherently susceptible to socioeconomic, environmental and cultural influences which change over time. Additionally, rapid leaps in technology have increased our understanding of the complex role of gene–environment interactions in life course health, highlighting the need for new cohort studies with repeated biological sampling and in-depth phenotype data across the first 1000 days of life from conception.Methods and analysis The Newcastle 1000 (NEW1000) Study, based in the regional city of Newcastle, New South Wales, was developed after an extensive consultation process involving 3 years of discussion with key stakeholders and healthcare consumer organisations and seven healthcare consumer workshops. This prospective population-based pregnancy cohort study will recruit 500 families per year for 5 years, providing detailed, longitudinal, multisystem phenotyping, repeated ultrasound measures and serial sample collection to investigate healthcare consumer identified health outcomes of priority. Stage 1 will involve recruitment of pregnant participants and their partners at 14 weeks gestation, with dense phenotype data and biological samples collected at 14, 20, 28 and 36 weeks gestation and serial ultrasound measures at 20, 28, 36 and 40 weeks, with postpartum follow-up at 6 weeks and 6 months. Biological samples will be used for biomarker discovery and sequencing of the genome, transcriptome, epigenome, microbiome and metabolome.Ethics and dissemination Ethics approval was obtained from Hunter New England Local Health District Ethics Committee (2020/ETH02881). Outcomes will be published in peer-reviewed journals, disseminated to participants through the NEW1000 website, presented at scientific conferences, and written reports to local, state and national government bodies and key stakeholders in the healthcare system to inform policy and evidence-based practice.

Subjects

Subjects :
Medicine

Details

Language :
English
ISSN :
20446055
Volume :
13
Issue :
7
Database :
Directory of Open Access Journals
Journal :
BMJ Open
Publication Type :
Academic Journal
Accession number :
edsdoj.1924df6211664567b65f03d9a26669ac
Document Type :
article
Full Text :
https://doi.org/10.1136/bmjopen-2023-072205