转化科学、DNA 商业化和知情同意:特定术语的必要性》,《H3Africa 项目回顾的启示》。

IF 1.3 4区 医学 Q4 GENETICS & HEREDITY Public Health Genomics Pub Date : 2022-01-25 DOI:10.1159/000521371
Patricia Marshall, Charmaine D M Royal, Ruth Chadwick
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引用次数: 0

摘要

在过去的十年中,基因组研究、其应用以及将其转化为医疗保健产品和服务以造福公众健康的进程不断加快。这些进展对于实现基因组研究在促进改善健康和疾病预防、诊断和治疗方面的潜力至关重要。尽管机遇巨大,但伴随着基因组研究商业化的蓬勃发展和日益全球化,各种伦理挑战和问题也随之而来。未经授权使用非洲人 DNA 样本开发 DNA 芯片的可能性扩大了对基因组研究中商业化、利益共享和适当同意的含义、意义和影响的讨论。非洲人类遗传与健康(H3Africa)联盟的领导召集了一个专家小组,审查 H3Africa 联盟项目中采用的研究伦理实践,并就商业化问题提出建议。18 位研究者提交了涉及数据共享和基因信息使用的项目文件。共审查了与这 18 个项目相关的 39 份知情同意书。所有 18 个项目都明确规定样本将用于未来的研究。只有不到一半的项目用文字说明样本可用于药物或产品开发,DNA 样本不会出售,利润也不会与参与者分享。有四个项目提到了商业化。对同意文件中包含的信息进行分析有助于开发商业化类型学。该类型学确定了有关特定商业化实例可接受性的考虑因素。用于产品开发转化研究的 DNA 样本需要一个透明的商业化框架,以便为同意程序提供信息。
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Translational Science, DNA Commercialization, and Informed Consent: The Need for Specific Terminology, Insights from a Review of H3Africa Projects.

In the past decade, there has been an acceleration in genomic research, its applications, and its translation into healthcare products and services for the benefit of public health. These advances are critical to realizing the potential of genomic research for facilitating improved health and disease prevention, diagnosis, and treatment. Despite its tremendous opportunities, the dynamic and increasingly global landscape of genomic research commercialization has been accompanied by a variety of ethical challenges and concerns. The potential for unauthorized use of DNA samples from African people to develop a DNA chip amplifies discussion on the meanings, implications, and impacts of commercialization, benefit sharing, and appropriate consent in genomic research. Leadership of the Human Heredity and Health in Africa (H3Africa) Consortium convened a panel of experts to review research ethics practices employed in H3Africa Consortium projects and make recommendations regarding commercialization. Eighteen investigators submitted documents for projects involving data sharing and use of genetic information. A total of 39 informed consent documents associated with the 18 projects were reviewed. All 18 projects specified that samples would be used in future research. Less than half of the projects included language noting that samples could be used in drug or product development, that DNA samples would not be sold, and that profits would not be shared with participants. Four projects referred to commercialization. Analysis of information included in consent documents contributed to the development of a Commercialization Typology. The Typology identifies factors to consider regarding acceptability of particular instances of commercialization. DNA samples for translational research in product development require a transparent commercialization framework to inform the consent process.

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来源期刊
Public Health Genomics
Public Health Genomics 医学-公共卫生、环境卫生与职业卫生
CiteScore
2.90
自引率
0.00%
发文量
14
审稿时长
>12 weeks
期刊介绍: ''Public Health Genomics'' is the leading international journal focusing on the timely translation of genome-based knowledge and technologies into public health, health policies, and healthcare as a whole. This peer-reviewed journal is a bimonthly forum featuring original papers, reviews, short communications, and policy statements. It is supplemented by topic-specific issues providing a comprehensive, holistic and ''all-inclusive'' picture of the chosen subject. Multidisciplinary in scope, it combines theoretical and empirical work from a range of disciplines, notably public health, molecular and medical sciences, the humanities and social sciences. In so doing, it also takes into account rapid scientific advances from fields such as systems biology, microbiomics, epigenomics or information and communication technologies as well as the hight potential of ''big data'' for public health.
期刊最新文献
"The Biggest Struggle:" Navigating Trust and Uncertainty in Genetic Variant Interpretation. "Should I let them know I have this?": Multifaceted genetic discrimination and limited awareness of legal protections amongst individuals with hereditary cancer syndromes. Who's on your genomics research team? Consumer experiences from Australia. Development and Pilot Testing of Evidence-Based Interventions to Improve Adherence after Receiving a Genetic Result. Co-creating the experience of consent for newborn genome sequencing (The Generation Study).
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