Faculty of Medicine, Memorial University, St. John's, Newfoundland, Canada.
Genet Med. 2012 Feb;14(2):229-35. doi: 10.1038/gim.0b013e31822e578f.
To assess the public's perception of biobank research and the relative importance they place on concerns for privacy and confidentiality, when compared with other key variables when considering participation in biobank research.
Conjoint analysis of three key attributes (research focus, research beneficiary, and privacy and confidentiality) under conditions of either blanket or specific consent.
Although the majority of our participants described themselves as private individuals, they consistently ranked privacy and confidentiality as the least important of the variables they considered. The potential beneficiary of proposed research ranked the highest under conditions of both blanket and specific consent. When completing the conjoint task under conditions of blanket consent, participants tended to act more altruistically.
The public tends to view biobanks as public goods designed primarily for public benefit. As such it tends to act altruistically with respect to the potential benefits that might accrue from research using biobanked samples. Participants expressed little concern about informational risks (i.e., privacy and confidentiality) should they choose to participate. The manner in which policy priorities are framed could impact participant value preferences with regard to a number of governance issues in biobanking.
评估公众对生物库研究的看法,以及在考虑参与生物库研究时,与其他关键变量相比,他们对隐私和保密性的重视程度。
在全有或全无同意的条件下,对三个关键属性(研究重点、研究受益人和隐私和保密性)进行联合分析。
尽管大多数参与者都将自己描述为私人个体,但他们始终将隐私和保密性列为他们考虑的变量中最不重要的因素。在全有或全无同意的条件下,拟议研究的潜在受益方排名最高。当参与者在全有同意的条件下完成联合任务时,他们往往表现出更利他的行为。
公众倾向于将生物库视为主要为公共利益设计的公共物品。因此,他们往往会对可能从使用生物库样本进行研究中获得的潜在利益表现出利他行为。如果参与者选择参与,他们对信息风险(即隐私和保密性)的关注较少。政策优先事项的制定方式可能会影响参与者对生物库治理问题的一些价值偏好。