Michie Marsha, Henderson Gail, Garrett Joanne, Corbie-Smith Giselle
University of North Carolina-Chapel Hill, Chapel Hill, NC 27599-8040, USA.
J Empir Res Hum Res Ethics. 2011 Jun;6(2):57-70. doi: 10.1525/jer.2011.6.2.57.
Human genome research depends upon participants who donate genetic samples, but few studies have explored in depth the motivations of genetic research donors. This mixed methods study examines telephone interviews with 752 sample donors in a U.S. genetic epidemiology study investigating colorectal cancer. Quantitative and qualitative results indicate that most participants wanted to help society, and that many also wanted information about their own health, even though such information was not promised. Qualitative analysis reveals that donors believed their samples contributed to a scientific "common good"; imagined samples as information rather than tissues; and often blurred distinctions between research and diagnostic testing of samples. Differences between African American and White perspectives were distinct from educational and other possible explanatory factors.
人类基因组研究依赖于捐赠基因样本的参与者,但很少有研究深入探讨基因研究捐赠者的动机。这项混合方法研究调查了美国一项针对结直肠癌的基因流行病学研究中的752名样本捐赠者的电话访谈。定量和定性结果表明,大多数参与者希望帮助社会,而且许多人也希望获得有关自身健康的信息,尽管并未承诺会提供此类信息。定性分析显示,捐赠者认为他们的样本有助于实现科学的“共同利益”;将样本视为信息而非组织;并且常常模糊样本研究与诊断测试之间的区别。非裔美国人和白人观点之间的差异与教育及其他可能的解释因素截然不同。