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后基因组时代的生物样本库治理

Biobank governance in the post-genomic age.

作者信息

Gottweis Herbert, Lauss Georg

机构信息

Department of Political Science, University of Vienna, Vienna, Austria.

出版信息

Per Med. 2010 Mar;7(2):187-195. doi: 10.2217/pme.10.4.

Abstract

Biobank governance is about the regulation of the relationship between individual citizens, society and biobanks. Its key agenda is to link society, citizens and biobanks with respect to issues of consent, privacy, ownership, access and benefit sharing. With the transformation of biobank research from local/national activities towards transnational projects and the emergence of post-genomic medical research, biobanks need to establish novel governance structures. We consider governance solutions that focus on 'bioethical-theoretical' arguments to be of only limited value in this context. By contrast, we think the key lies in developing participatory arrangements that are responsive to the views of patients and 'lay people', and also operate on a transnational level. The social-political and communicative competence of biobank infrastructures must be improved, thereby assuring the long-term legitimacy and commitment to these often highly expensive projects from a large variety of different stakeholders over the decades.

摘要

生物样本库治理涉及对个体公民、社会与生物样本库之间关系的规范。其核心议程是在同意、隐私、所有权、获取和利益分享等问题上,将社会、公民和生物样本库联系起来。随着生物样本库研究从地方/国家活动向跨国项目转变,以及后基因组医学研究的兴起,生物样本库需要建立新的治理结构。我们认为,在这种背景下,专注于“生物伦理理论”论据的治理解决方案价值有限。相比之下,我们认为关键在于制定参与性安排,这些安排要能回应患者和“普通民众”的观点,并且在跨国层面上运作。必须提高生物样本库基础设施的社会政治和沟通能力,从而确保在几十年里,来自各种不同利益相关者的对这些通常成本高昂的项目的长期合法性和承诺。

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