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[对生物样本库中储存多年的血液样本进行的基因研究。大多数人愿意提供知情同意书]

[Genetic research on blood samples stored for years in biobanks. Most people are willing to provide informed consent].

作者信息

Stegmayr Birgitta, Asplund Kjell

机构信息

Institutionen för folkhälsa och klinisk medicin, Norrlands Universitetssjukhus, Umea.

出版信息

Lakartidningen. 2003 Feb 20;100(8):618-20.

PMID:12640974
Abstract

Genetic research involving biobanks has been the subject of numerous declarations, recommendations and guidelines produced by professionals, administrators, legislators and other decision-makers. Yet, there is little published empirical information on people's willingness to participate in genetic studies on blood samples that they donated many years ago, at a time when the informed consent did not include the possibility of genetic research. We here report on our experiences of obtaining informed consent for academic and as well as commercial genetic research on blood samples collected more than a decade ago. Participants in a population-based risk factor survey who had donated blood to a biobank in 1990 were contacted eleven years later (in 2001) and asked for informed consent for genetic studies. A total of 1,311 out of 1,409 participants (93%) gave their consent to use blood samples for academic genetic research, provided that an Ethics Committee had approved the research. Thirty-one participants (2.2%) did not give their consent for academic genetic research. Another 35 subjects (2.5%) did not consent to industrial genetic research even if their blood samples were anonymized. Sixty-four individuals did not reply or provided incomplete answers (together 4.8%). Of the 1,311 individuals that agreed to participate, 292 (22.3%) wanted to be informed and give their concent to every new specific project. All the others gave a general concent provided that an Ethics Committee had approved the research.

摘要

涉及生物样本库的基因研究一直是专业人士、管理人员、立法者及其他决策者发布的众多声明、建议和指导方针的主题。然而,关于人们是否愿意参与多年前捐赠血液样本的基因研究的实证信息却鲜有发表,因为当时的知情同意并不包括基因研究的可能性。我们在此报告我们在获取对十多年前采集的血液样本进行学术及商业基因研究的知情同意方面的经验。1990年向一个生物样本库献血的基于人群的风险因素调查参与者在11年后(2001年)被联系,并被要求对基因研究给予知情同意。在1409名参与者中,共有1311人(93%)同意在伦理委员会批准研究的前提下,将血液样本用于学术基因研究。31名参与者(2.2%)不同意进行学术基因研究。另外35名受试者(2.5%)即使其血液样本已匿名化,也不同意进行商业基因研究。64人未回复或提供不完整答案(共4.8%)。在同意参与的1311人中,292人(22.3%)希望收到通知并对每个新的具体项目给予同意。其他所有人在伦理委员会批准研究的前提下给予了一般同意。

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引用本文的文献

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Consent for the use of human biological samples for biomedical research: a mixed methods study exploring the UK public's preferences.同意使用人类生物样本进行生物医学研究:一项探索英国公众偏好的混合方法研究。
BMJ Open. 2013 Aug 7;3(8):e003022. doi: 10.1136/bmjopen-2013-003022.
2
Biobanks for genomics and genomics for biobanks.用于基因组学的生物样本库以及用于生物样本库的基因组学。
Comp Funct Genomics. 2003;4(6):628-34. doi: 10.1002/cfg.333.
3
Different types--different rights. Distinguishing between different perspectives on ownership of biological material.
不同类型——不同权利。区分关于生物材料所有权的不同观点。
Sci Eng Ethics. 2007 Jun;13(2):221-33. doi: 10.1007/s11948-007-9005-x.
4
Consent and anonymization in research involving biobanks: differing terms and norms present serious barriers to an international framework.涉及生物样本库的研究中的同意与匿名化:不同的术语和规范给国际框架带来了严重障碍。
EMBO Rep. 2006 Jul;7(7):661-6. doi: 10.1038/sj.embor.7400740.
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Bodily rights and property rights.身体权和财产权。
J Med Ethics. 2006 Apr;32(4):209-14. doi: 10.1136/jme.2004.011270.