Department of Health Services, University of Washington School of Public Health, WA, USA.
J Law Med Ethics. 2011 Fall;39(3):502-12. doi: 10.1111/j.1748-720X.2011.00617.x.
Genetic research aimed at understanding human health and disease is grounded in the study of genetic variation. The inclusion of research subjects with diverse ancestral backgrounds is essential for genetic and genomic research that fully explores human diversity. Large-scale cohort studies and biobanks in Europe and the United States often do not include the breadth of ethnic and racial diversity observed in their countries' citizens. This article explores the findings of a qualitative study of U.S. scientists' understanding and views of the NIH Policy and Guidelines on the Inclusion of Minorities as Subjects in Clinical Research. The findings suggest that the policy restricts how scientists use racial and ethnic categories to define and report their study populations and does little to motivate their efforts to increase the inclusion of non-European ancestral populations in genetic and genomic research.
旨在理解人类健康和疾病的遗传研究基于对遗传变异的研究。纳入具有不同祖先背景的研究对象对于充分探索人类多样性的遗传和基因组研究至关重要。欧洲和美国的大规模队列研究和生物库通常不包括其国家公民所观察到的种族和民族多样性的广度。本文探讨了对美国科学家对 NIH 政策和准则的理解和看法的定性研究的结果,该政策和准则规定了少数群体作为临床研究对象的纳入。研究结果表明,该政策限制了科学家如何使用种族和民族类别来定义和报告他们的研究人群,并且几乎没有促使他们努力增加非欧洲祖先人群在遗传和基因组研究中的纳入。