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澳大利亚国家基因组数据治理框架的机遇:一项系统综述

Opportunities for a national genomic data governance framework in Australia: a systematic review.

作者信息

Cannizzo Fabian, Vidgen Miranda E, McWhirter Rebekah, Petersen Alan, Otlowski Margaret, Rizzi Marco, Hensley Jasmine, Newson Ainsley J

机构信息

School of Social Sciences, Faculty of Arts, Monash University, Clayton, VIC, 3800, Australia.

QIMR Berghofer, Herston, QLD, 4006, Australia.

出版信息

BMC Med Ethics. 2025 Aug 14;26(1):111. doi: 10.1186/s12910-025-01273-7.

Abstract

BACKGROUND

As with other countries, Australia is seeking to make efficient use of genomic data for use in research, clinical medicine and population health. However, to enable cross jurisdictional consistency in the management of and access to data, it will first need to establish a national framework for governing genomic data. To this end, ethical, legal and social issues are often discussed. However, the literature offers little evidence-based support for such a framework.

METHODS

To address this literature gap, we systematically reviewed two databases (Scopus and PubMed) for research articles that discussed issues and opportunities for enacting genomic data governance frameworks in the domains of research, genomic medicine and public (population) health in the Australian context.

RESULTS

Thirty-one relevant articles were included and were analysed using inductive content analysis. Our findings identified that opportunities for implementing a national genomic data governance framework concerned defining roles for patients in data governance, data management processes and increasing the public acceptance of genomic data use in healthcare and research. Additionally, they highlight differences in the opportunities and priorities for clinical and research genomics that hinder further advancement of data governance.

CONCLUSIONS

Our synthesis of the current literature on genomic data governance suggests that the current focus on individual consent as the primary mechanism for protecting data subjects and different priorities in clinical and research governance need to be addressed. Given the significance of the role of consent procedures and differences in clinical and research data in generating a data governance framework, our findings hence reveal a critical gap in the research literature. Advancing a national genomic data governance framework will require greater consensus and clarity regarding the application of ethical principles across jurisdictions and institutions.

摘要

背景

与其他国家一样,澳大利亚正寻求有效利用基因组数据用于研究、临床医学和人群健康。然而,为了在数据管理和获取方面实现跨辖区的一致性,首先需要建立一个管理基因组数据的国家框架。为此,人们经常讨论伦理、法律和社会问题。然而,文献中几乎没有基于证据的支持此类框架的内容。

方法

为了填补这一文献空白,我们系统地检索了两个数据库(Scopus和PubMed),以查找在澳大利亚背景下讨论在研究、基因组医学和公共(人群)健康领域制定基因组数据治理框架的问题和机遇的研究文章。

结果

纳入了31篇相关文章,并采用归纳性内容分析法进行分析。我们的研究结果表明,实施国家基因组数据治理框架的机遇包括确定患者在数据治理中的角色、数据管理流程以及提高公众对在医疗保健和研究中使用基因组数据的接受度。此外,这些结果还凸显了临床和研究基因组学在机遇和优先事项上的差异,这些差异阻碍了数据治理的进一步发展。

结论

我们对当前关于基因组数据治理的文献进行的综合分析表明,当前将个人同意作为保护数据主体的主要机制的重点以及临床和研究治理中的不同优先事项需要得到解决。鉴于同意程序的作用以及临床和研究数据在生成数据治理框架方面的差异的重要性,我们的研究结果因此揭示了研究文献中的一个关键空白。推进国家基因组数据治理框架将需要在跨辖区和机构应用伦理原则方面达成更大的共识并提高清晰度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7165/12355800/af552083d8ff/12910_2025_1273_Fig1_HTML.jpg

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