Benefit-Sharing by Design: A Call to Action for Human Genomics Research

IF 7.7 2区 生物学 Q1 GENETICS & HEREDITY Annual review of genomics and human genetics Pub Date : 2024-04-12 DOI:10.1146/annurev-genom-021623-104241
Ann M. Mc Cartney, Amber Hartman Scholz, Mathieu Groussin, Ciara Staunton
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Abstract

The ethical standards for the responsible conduct of human research have come a long way; however, concerns surrounding equity remain in human genetics and genomics research. Addressing these concerns will help society realize the full potential of human genomics research. One outstanding concern is the fair and equitable sharing of benefits from research on human participants. Several international bodies have recognized that benefit-sharing can be an effective tool for ethical research conduct, but international laws, including the Convention on Biological Diversity and its Nagoya Protocol on Access and Benefit-Sharing, explicitly exclude human genetic and genomic resources. These agreements face significant challenges that must be considered and anticipated if similar principles are applied in human genomics research. We propose that benefit-sharing from human genomics research can be a bottom-up effort and embedded into the existing research process. We propose the development of a “benefit-sharing by design” framework to address concerns of fairness and equity in the use of human genomic resources and samples and to learn from the aspirations and decade of implementation of the Nagoya Protocol.
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利益共享设计:人类基因组研究行动呼吁书
负责任地开展人类研究的伦理标准已经取得了长足的进步,但在人类遗传学和基因组学研究中,与公平有关的问题依然存在。解决这些问题将有助于社会充分发挥人类基因组学研究的潜力。一个突出的问题是如何公平公正地分享人类参与研究带来的利益。一些国际机构已经认识到,利益共享可以成为符合伦理的研究行为的有效工具,但包括《生物多样性公约》及其《获取和利益共享名古屋议定书》在内的国际法明确将人类基因和基因组资源排除在外。如果要在人类基因组学研究中应用类似的原则,就必须考虑和预见这些协议所面临的重大挑战。我们建议,人类基因组学研究的惠益分享可以是一种自下而上的努力,并纳入现有的研究过程。我们建议制定一个 "设计利益共享 "框架,以解决人类基因组资源和样本使用中的公平和公正问题,并从《名古屋议定书》的愿望和十年实施过程中吸取经验教训。
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来源期刊
CiteScore
14.90
自引率
1.10%
发文量
29
期刊介绍: Since its inception in 2000, the Annual Review of Genomics and Human Genetics has been dedicated to showcasing significant developments in genomics as they pertain to human genetics and the human genome. The journal emphasizes genomic technology, genome structure and function, genetic modification, human variation and population genetics, human evolution, and various aspects of human genetic diseases, including individualized medicine.
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