Data resource profile: the ORIGINS project databank: a collaborative data resource for investigating the developmental origins of health and disease.

IF 2.2 Q3 HEALTH CARE SCIENCES & SERVICES
International Journal of Population Data Science Pub Date : 2024-09-30 eCollection Date: 2023-01-01 DOI:10.23889/ijpds.v8i6.2388
Belinda C Davey, Wesley Billingham, Jacqueline A Davis, Lisa Gibson, Nina D'Vaz, Susan L Prescott, Desiree T Silva, Sarah Whalan
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引用次数: 0

Abstract

Introduction: The ORIGINS Project ("ORIGINS") is a longitudinal, population-level birth cohort with data and biosample collections that aim to facilitate research to reduce non-communicable diseases (NCDs) and encourage 'a healthy start to life'. ORIGINS has gathered millions of datapoints and over 400,000 biosamples over 15 timepoints, antenatally through to five years of age, from mothers, non-birthing partners and the child, across four health and wellness domains: 'Growth and development', 'Medical, biological and genetic', 'Biopsychosocial and cognitive', 'Lifestyle, environment and nutrition'.

Methods: Mothers, non-birthing partners and their offspring were recruited antenatally (between 18 and 38 weeks' gestation) from the Joondalup and Wanneroo communities of Perth, Western Australia from 2017 to 2024. Data come from several sources, including routine hospital antenatal and birthing data, ORIGINS clinical appointments, and online self-completed surveys comprising several standardised measures. Data are merged using the Medical Record Number (MRN), the ORIGINS Unique Identifier and the ORIGINS Pregnancy Number, as well as additional demographic data (e.g. name and date of birth) when necessary.

Results: The data are held on an integrated data platform that extracts, links, ingests, integrates and stores ORIGINS' data on an Amazon Web Services (AWS) cloud-based data warehouse. Data are linked, transformed for cleaning and coding, and catalogued, ready to provide to sub-projects (independent researchers that apply to use ORIGINS data) to prepare for their own analyses. ORIGINS maximises data quality by checking and replacing missing and erroneous data across the various data sources.

Conclusion: As a wide array of data across several different domains and timepoints has been collected, the options for future research and utilisation of the data and biosamples are broad. As ORIGINS aims to extend into middle childhood, researchers can examine which antenatal and early childhood factors predict middle childhood outcomes. ORIGINS also aims to link to State and Commonwealth data sets (e.g. Medicare, the National Assessment Program - Literacy and Numeracy, the Pharmaceutical Benefits Scheme) which will cater to a wide array of research questions.

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数据资源简介:ORIGINS 项目数据库:研究健康和疾病发育起源的合作数据资源。
前言:ORIGINS项目(“ORIGINS“)是一个人口水平的纵向出生队列,收集数据和生物样本,旨在促进减少非传染性疾病的研究,并鼓励”健康的生命之初”。ORIGINS收集了从产前到5岁的15个时间点的数百万个数据点和40多万份生物样本,来自母亲、非生育伴侣和儿童,涉及四个健康和保健领域:“生长和发育”、“医学、生物和遗传”、“生物、心理、社会和认知”、“生活方式、环境和营养”。方法:2017年至2024年,从西澳大利亚珀斯Joondalup和Wanneroo社区招募母亲、非生育伴侣及其后代(妊娠18至38周)。数据来自多个来源,包括常规医院产前和分娩数据、ORIGINS临床预约以及包含若干标准化措施的在线自填调查。在必要时,使用医疗记录号(MRN)、ORIGINS唯一标识符和ORIGINS妊娠编号以及其他人口统计数据(例如姓名和出生日期)合并数据。结果:数据保存在一个集成的数据平台上,该平台在基于亚马逊网络服务(AWS)的云数据仓库中提取、链接、摄取、集成和存储ORIGINS的数据。数据被链接、转换以进行清理和编码,并进行编目,准备提供给子项目(申请使用ORIGINS数据的独立研究人员),以便为他们自己的分析做准备。ORIGINS通过检查和替换各种数据源中的缺失和错误数据来最大限度地提高数据质量。结论:由于收集了多个不同领域和时间点的广泛数据,因此未来研究和利用数据和生物样本的选择是广泛的。由于ORIGINS旨在扩展到儿童中期,研究人员可以检查哪些产前和早期儿童因素可以预测儿童中期的结果。ORIGINS还旨在与州和联邦的数据集(例如医疗保险、国家评估计划-识字和算术、药品福利计划)建立联系,这将满足广泛的研究问题。
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0.00%
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