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本文引用的文献

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Return of research results from genomic biobanks: cost matters.基因组生物样本库研究结果的反馈:成本很重要。
Genet Med. 2013 Feb;15(2):103-5. doi: 10.1038/gim.2012.105. Epub 2012 Aug 30.
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Population studies: return of research results and incidental findings Policy Statement.人群研究:研究结果和偶然发现的回报政策声明。
Eur J Hum Genet. 2013 Mar;21(3):245-7. doi: 10.1038/ejhg.2012.152. Epub 2012 Jul 11.
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To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.是否告知?遗传学背景下偶然发现的伦理思考系统综述。
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Managing incidental findings and research results in genomic research involving biobanks and archived data sets.管理涉及生物库和存档数据集的基因组研究中的偶发发现和研究结果。
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Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study.公众对个体基因研究结果返还的偏好:一项定性焦点小组研究的结果。
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Practical implementation issues and challenges for biobanks in the return of individual research results.生物银行在个体研究结果回报方面的实际实施问题和挑战。
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What research participants want to know about genetic research results: the impact of "genetic exceptionalism".研究参与者想了解的关于基因研究结果的内容:“基因例外论”的影响。
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Disclosure of individual genetic data to research participants: the debate reconsidered.向研究参与者披露个体基因数据:重新审议该争议。
Trends Genet. 2011 Feb;27(2):41-7. doi: 10.1016/j.tig.2010.11.004. Epub 2010 Dec 27.
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The return of individual research findings in paediatric genetic research.儿科遗传研究中个体研究结果的回报。
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Communication of biobanks' research results: what do (potential) participants want?生物银行研究结果的交流:(潜在)参与者想要什么?
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偶然发现:制定生物样本库政策的时机尚不成熟。

Incidental findings: the time is not yet ripe for a policy for biobanks.

作者信息

Viberg Jennifer, Hansson Mats G, Langenskiöld Sophie, Segerdahl Pär

机构信息

Department of Public Health and Caring Sciences, Centre for Research Ethics & Bioethics, Uppsala University, Uppsala, Sweden.

Department of Public Health and Caring Sciences, Health Economics, Uppsala University, Uppsala, Sweden.

出版信息

Eur J Hum Genet. 2014 Apr;22(4):437-41. doi: 10.1038/ejhg.2013.217. Epub 2013 Sep 25.

DOI:10.1038/ejhg.2013.217
PMID:24065111
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3953922/
Abstract

Incidental findings (IFs) are acknowledged to be among the most important ethical issues to consider in biobank research. Genome-wide association studies and disease-specific genetic research might reveal information about individual participants that are not related to the research purpose, but may be relevant to those participants' future health. In this article, we provide a synopsis of arguments for and against the disclosure of IFs in biobank research. We argue that arguments that do not distinguish between communications about pathogenic conditions and complex genetic risk for diseases fail, as preferences and decisions may be far more complex in the latter case. The principle of beneficence, for example, often supports the communication of incidentally discovered diseases, but if communication of risk is different, the beneficence of such communication is not equally evident. By conflating the latter form of communication with the former, the application of ethical principles to IFs in biobank research sometimes becomes too easy and frictionless. Current empirical surveys of people's desire to be informed about IFs do not provide sufficient guidance because they rely on the same notion of risk communication as a form of communication about actual health and disease. Differently designed empirical research and more reflection on biobank research and genetic risk information is required before ethical principles can be applied to support the adoption of a reasonable and comprehensive policy for handling IFs.

摘要

偶然发现(IFs)被认为是生物样本库研究中需要考虑的最重要的伦理问题之一。全基因组关联研究和特定疾病的基因研究可能会揭示与个体参与者相关但与研究目的无关的信息,但这些信息可能与参与者未来的健康状况有关。在本文中,我们概述了支持和反对在生物样本库研究中披露偶然发现的观点。我们认为,那些没有区分关于致病状况的沟通和疾病复杂遗传风险的沟通的观点是站不住脚的,因为在后一种情况下,偏好和决策可能要复杂得多。例如,行善原则通常支持传达偶然发现的疾病,但如果风险沟通不同,这种沟通的行善性就不那么明显了。通过将后一种沟通形式与前一种混为一谈,伦理原则在生物样本库研究中对偶然发现的应用有时变得过于简单和顺畅。目前关于人们希望了解偶然发现的实证调查没有提供足够的指导,因为它们依赖于与关于实际健康和疾病的沟通相同的风险沟通概念。在伦理原则能够应用于支持采用合理和全面的偶然发现处理政策之前,需要进行不同设计的实证研究,并对生物样本库研究和基因风险信息进行更多反思。