Enhancing Equity in Genomics: Incorporating Measures of Structural Racism, Discrimination, and Social Determinants of Health

IF 2.3 3区 哲学 Q1 ETHICS Hastings Center Report Pub Date : 2024-12-21 DOI:10.1002/hast.4927
Ramya M. Rajagopalan, Matteo D'Antonio, Joan H. Fujimura
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Abstract

The everyday harms of structural racism and discrimination, perpetuated through institutions, laws, policies, and practices, constitute social determinants of health, but measures that account for their debilitating effects are largely missing in genetic studies of complex diseases. Drawing on insights from the social sciences and public health, we propose critical methodologies for incorporating tools that measure structural racism and discrimination within genetic analyses. We illustrate how including these measures may strengthen the accuracy and utility of findings for diverse communities, clarify elusive relationships between genetics and environment in a racialized society, and support greater equity within genomics and precision health research. This approach may also support efforts to build and sustain vital partnerships with communities and with other fields of research inquiry, centering community expertise and lived experiences and drawing on valuable knowledge from practitioners in the social sciences and public health to innovate biomedical and genomic study designs aimed at community health priorities.

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增强基因组学的公平性:结合结构性种族主义、歧视和健康的社会决定因素的措施
结构性种族主义和歧视的日常危害,通过制度、法律、政策和实践得以延续,构成了健康的社会决定因素,但在复杂疾病的遗传研究中,大多缺乏解释其衰弱影响的措施。借鉴社会科学和公共卫生的见解,我们提出了在遗传分析中纳入测量结构性种族主义和歧视的工具的关键方法。我们说明了包括这些措施如何加强不同社区研究结果的准确性和实用性,澄清种族化社会中遗传学和环境之间难以捉摸的关系,并支持基因组学和精确健康研究中更大的公平性。这一办法还可支持努力与社区和其他研究调查领域建立和维持重要的伙伴关系,以社区专门知识和生活经验为中心,利用社会科学和公共卫生从业人员的宝贵知识,创新旨在社区卫生优先事项的生物医学和基因组研究设计。
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来源期刊
Hastings Center Report
Hastings Center Report 医学-卫生保健
CiteScore
3.50
自引率
3.00%
发文量
99
审稿时长
6-12 weeks
期刊介绍: The Hastings Center Report explores ethical, legal, and social issues in medicine, health care, public health, and the life sciences. Six issues per year offer articles, essays, case studies of bioethical problems, columns on law and policy, caregivers’ stories, peer-reviewed scholarly articles, and book reviews. Authors come from an assortment of professions and academic disciplines and express a range of perspectives and political opinions. The Report’s readership includes physicians, nurses, scholars, administrators, social workers, health lawyers, and others.
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