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靶向代表性:解读精准医学研究中对多样性的呼吁。

Targeting Representation: Interpreting Calls for Diversity in Precision Medicine Research.

机构信息

Division of Ethics, Department of Medical Humanities and Ethics, Columbia University, New York, NY, USA.

Department of Bioethics & Humanities, School of Medicine, University of Washington, Seattle, WA, USA.

出版信息

Yale J Biol Med. 2022 Sep 30;95(3):317-326. eCollection 2022 Sep.

Abstract

Scientists have identified a "diversity gap" in genetic samples and health data, which have been drawn predominantly from individuals of European ancestry, as posing an existential threat to the promise of precision medicine. Inadequate inclusion as articulated by scientists, policymakers, and ethicists has prompted large-scale initiatives aimed at recruiting populations historically underrepresented in biomedical research. Despite explicit calls to increase diversity, the meaning of diversity - which dimensions matter for what outcomes and why - remain strikingly imprecise. Drawing on our document review and qualitative data from observations and interviews of funders and research teams involved in five precision medicine research (PMR) projects, we note that calls for increasing diversity often focus on "representation" as the goal of recruitment. The language of representation is used flexibly to refer to two objectives: achieving sufficient genetic variation across populations and including historically disenfranchised groups in research. We argue that these dual understandings of representation are more than rhetorical slippage, but rather allow for the contemporary collection of samples and data from marginalized populations to stand in as correcting historical exclusion of social groups towards addressing health inequity. We trace the unresolved historical debates over how and to what extent researchers should procure diversity in PMR and how they contributed to ongoing uncertainty about what axes of diversity matter and why. We argue that ambiguity in the meaning of representation at the outset of a study contributes to a lack of clear conceptualization of diversity downstream throughout subsequent phases of the study.

摘要

科学家们已经发现,遗传样本和健康数据中存在“多样性差距”,这些数据主要来自欧洲血统的个体,这对精准医学的承诺构成了生存威胁。科学家、政策制定者和伦理学家认为,这种代表性不足是存在问题的,因此已经提出了大规模的倡议,旨在招募在生物医学研究中代表性不足的人群。尽管人们明确呼吁增加多样性,但多样性的含义——哪些维度对哪些结果重要,以及为什么重要——仍然非常不精确。通过对我们的文件审查以及对参与五个精准医学研究 (PMR) 项目的资助者和研究团队的观察和访谈的定性数据的分析,我们注意到,增加多样性的呼吁通常侧重于“代表性”作为招募的目标。代表性的语言被灵活地用于指代两个目标:在人群中实现足够的遗传变异,以及将历史上被剥夺权利的群体纳入研究。我们认为,这两种对代表性的理解不仅仅是修辞上的失误,而是允许当代从边缘化人群中收集样本和数据,以纠正历史上对社会群体的排斥,从而解决健康不平等问题。我们追溯了在 PMR 中,研究人员应该如何以及在多大程度上获取多样性的历史上存在争议的问题,以及这些争议如何导致了人们对多样性的哪些轴重要以及为什么重要的持续不确定性。我们认为,在研究开始时代表性的含义不明确,导致在研究的后续阶段,缺乏对多样性的明确概念化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1512/9511949/a260db69f670/yjbm_95_3_317_g01.jpg

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