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Citizens' conceptions of the genome: Related values and practical implications in a citizen forum on the use of genomic information

机译:公民的基因组的概念:在使用基因组信息的公民论坛中相关价值观和实际意义

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Background The development of large data sets, including genomic data, coupled with rapid advances in personalized medicine where citizens increasingly face complex choices about the use of their genomic information implies that citizens are essential stakeholders in genomics. They should be engaged in the ethical, legal and societal issues to produce a framework that fosters trust and allows them to guide the technology based on their values. Objective This article highlights that citizens' conceptions of the human genome inform about and make sense of their main values regarding the use of genomic information, which is critical for policymakers, experts and stakeholders to understand to maintain the public support in genomics. Method Through an inductive thematic approach, we reanalysed data collected for the Belgian citizen forum, which aimed to produce recommendations for the Ministry of Public Health and other stakeholders. Results Citizens expressed four conceptions of the genome that determined which uses of genomic information they supported: the most intimate part of individuals; ‘I am more than my genome’; the individual's property vs the common good; and uncertainty and fear. Conclusion Diversity in their conceptions reveals remaining conflicts of values among citizens, mainly regarding a conception of the genome as an individual property or a common good. However, despite differing conceptions, shared values emerged such as solidarity, privacy, no genetic discrimination and the right to an open future, where individual and common interests coexist. Patient or public contribution The panel of the citizen forum consisted of 32 citizens.
机译:背景技术大型数据集的发展,包括基因组数据,加上个性化医学的快速进步,公民日益面临复杂的选择与其基因组信息的使用意味着公民是基因组学中的基本利益相关者。他们应该从事道德,法律和社会问题,以产生促进信任的框架,并允许他们根据其价值来指导技术。目的突出显示人类基因组的公民的概念,了解并对基因组信息使用的主要价值观,这对于政策制定者,专家和利益相关者来说至关重要,以了解维持基因组织的公众支持。方法通过归纳专题方法,我们为比利时公民论坛收集的数据进行了成绩,旨在为公共卫生和其他利益攸关方提供建议。结果公民表达了该基因组的四个概念,确定了他们支持的基因组信息的哪些用途:个人最亲密的部分; “我不仅仅是我的基因组;个人的财产与共同的好处;和不确定性和恐惧。结论其概念的多样性揭示了公民之间的价值突破,主要是基因组的概念作为个人财产或共同的利益。但是,尽管有不同的概念,但共同的价值观出现了,如团结,隐私,没有遗传歧视以及个人和共同利益共存的公开未来的权利。患者或公共贡献公民论坛小组由32名公民组成。

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