Suppr超能文献

纳入少数族裔和少数民族参与遗传研究:通过改变规则来推进精神?

Inclusion of racial and ethnic minorities in genetic research: advance the spirit by changing the rules?

机构信息

Department of Health Services, University of Washington School of Public Health, WA, USA.

出版信息

J Law Med Ethics. 2011 Fall;39(3):502-12. doi: 10.1111/j.1748-720X.2011.00617.x.

Abstract

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.

摘要

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。

相似文献

引用本文的文献

8
Privacy and ethical challenges in next-generation sequencing.下一代测序中的隐私和伦理挑战。
Expert Rev Precis Med Drug Dev. 2019;4(2):95-104. doi: 10.1080/23808993.2019.1599685. Epub 2019 Apr 8.

本文引用的文献

7
The A's, G's, C's, and T's of health disparities.健康差异中的A、G、C和T
BMC Med Genomics. 2009 May 22;2:29. doi: 10.1186/1755-8794-2-29.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验