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Newcastle 1000 (NEW1000) Study: an Australian population-based prospective pregnancy cohort study design and protocol
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 socio...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351266/ https://www.ncbi.nlm.nih.gov/pubmed/37451724 http://dx.doi.org/10.1136/bmjopen-2023-072205 |
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author | Grace, Tegan Fisher, Joshua Wang, Carol Valkenborghs, Sarah R Smith, Roger Hirst, Jonathan J Mattes, Joerg Murphy, Vanessa E Pennell, Craig E |
author_facet | Grace, Tegan Fisher, Joshua Wang, Carol Valkenborghs, Sarah R Smith, Roger Hirst, Jonathan J Mattes, Joerg Murphy, Vanessa E Pennell, Craig E |
author_sort | Grace, Tegan |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10351266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-103512662023-07-18 Newcastle 1000 (NEW1000) Study: an Australian population-based prospective pregnancy cohort study design and protocol Grace, Tegan Fisher, Joshua Wang, Carol Valkenborghs, Sarah R Smith, Roger Hirst, Jonathan J Mattes, Joerg Murphy, Vanessa E Pennell, Craig E BMJ Open Obstetrics and Gynaecology 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. BMJ Publishing Group 2023-07-14 /pmc/articles/PMC10351266/ /pubmed/37451724 http://dx.doi.org/10.1136/bmjopen-2023-072205 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Obstetrics and Gynaecology Grace, Tegan Fisher, Joshua Wang, Carol Valkenborghs, Sarah R Smith, Roger Hirst, Jonathan J Mattes, Joerg Murphy, Vanessa E Pennell, Craig E Newcastle 1000 (NEW1000) Study: an Australian population-based prospective pregnancy cohort study design and protocol |
title | Newcastle 1000 (NEW1000) Study: an Australian population-based prospective pregnancy cohort study design and protocol |
title_full | Newcastle 1000 (NEW1000) Study: an Australian population-based prospective pregnancy cohort study design and protocol |
title_fullStr | Newcastle 1000 (NEW1000) Study: an Australian population-based prospective pregnancy cohort study design and protocol |
title_full_unstemmed | Newcastle 1000 (NEW1000) Study: an Australian population-based prospective pregnancy cohort study design and protocol |
title_short | Newcastle 1000 (NEW1000) Study: an Australian population-based prospective pregnancy cohort study design and protocol |
title_sort | newcastle 1000 (new1000) study: an australian population-based prospective pregnancy cohort study design and protocol |
topic | Obstetrics and Gynaecology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351266/ https://www.ncbi.nlm.nih.gov/pubmed/37451724 http://dx.doi.org/10.1136/bmjopen-2023-072205 |
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