Interrogating the Value of Return of Results for Diverse Populations: Perspectives from Precision Medicine Researchers.

Q1 Arts and Humanities AJOB Empirical Bioethics Pub Date : 2024-04-01 Epub Date: 2023-11-14 DOI:10.1080/23294515.2023.2279965
Caitlin E McMahon, Nicole Foti, Melanie Jeske, William R Britton, Stephanie M Fullerton, Janet K Shim, Sandra Soo-Jin Lee
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Abstract

Background: Over the last decade, the return of results (ROR) in precision medicine research (PMR) has become increasingly routine. Calls for individual rights to research results have extended the "duty to report" from clinically useful genetic information to traits and ancestry results. ROR has thus been reframed as inherently beneficial to research participants, without a needed focus on who benefits and how. This paper addresses this gap, particularly in the context of PMR aimed at increasing participant diversity, by providing investigator and researcher perspectives on and questions about the assumed value of ROR in PMR.

Methods: Semi-structured interviews with a purposive sample of investigators and researchers across federally funded PMR studies in three national consortia, as well as observations of study activities, focused on how PM researchers conceptualize diversity and implement inclusive practices across research stages, including navigating ROR.

Results: Interviewees (1) validated the value of ROR as a benefit of PMR, while others (2) questioned the benefit of clinically actionable results to individuals in the absence of sufficient resources for translating findings into health care for diverse and disadvantaged populations; (3) expressed uncertainties in applying the presumed value of ROR as a benefit for non-clinical results; and (4) and debated when the promise of the value of ROR may undermine trust in PMR, and divert efforts to return value beyond ROR.

Conclusions: Conceptualizations of diversity and inclusion among PM researchers and investigators raise unique ethical questions where unexamined assumptions of the value of ROR inform study recruitment efforts to enroll minoritized and under-represented populations. A lack of consideration for resources and infrastructure necessary to translate ROR into actionable information may hinder trustworthy community-research relationships. Thus, we argue for a more intentional interrogation of ROR practices as an offer of benefit and for whom.

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对不同人群结果返回值的质疑:来自精准医学研究人员的观点。
背景:在过去的十年中,精确医学研究(PMR)的结果返回(ROR)已经变得越来越常规。对研究结果个人权利的呼吁已经将“报告义务”从临床有用的遗传信息扩展到特征和祖先结果。因此,ROR被重新定义为对研究参与者本身有益,而没有必要关注谁受益以及如何受益。本文通过提供研究者和研究者对PMR中ROR的假设价值的观点和问题,解决了这一差距,特别是在PMR旨在增加参与者多样性的背景下。方法:对三个国家联盟中联邦资助的PMR研究的调查人员和研究人员进行半结构化访谈,以及对研究活动的观察,重点关注PM研究人员如何概念化多样性并实施跨研究阶段的包容性实践,包括导航ROR。结果:受访者(1)证实了ROR作为PMR益处的价值,而其他人(2)质疑在缺乏足够资源将研究结果转化为各种弱势群体的医疗保健的情况下,临床可操作结果对个人的益处;(3)表达了将ROR的假定值作为非临床结果的获益的不确定性;(4)并讨论了ROR价值的承诺何时会破坏对PMR的信任,并转移人们对ROR之外的回报价值的努力。结论:项目管理研究人员和调查人员对多样性和包容性的概念化提出了独特的伦理问题,其中未经检验的ROR价值假设为研究招募工作提供了信息,以招募少数族裔和代表性不足的人群。缺乏对将ROR转化为可操作信息所需的资源和基础设施的考虑,可能会阻碍值得信赖的社区研究关系。因此,我们主张对ROR实践进行更有意的询问,将其作为一种利益的提供以及为谁提供。
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来源期刊
AJOB Empirical Bioethics
AJOB Empirical Bioethics Arts and Humanities-Philosophy
CiteScore
3.90
自引率
0.00%
发文量
21
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