在基因组研究中代表性不足的人口:研究人员观点的定性研究
Arian Omeranovic1, Flora Nguyen Van Long1, Asma Boubaker1
1Oncology Division, CHU de Québec-Université Laval Research Center, Hôpital du Saint-Sacrement, 1050, Chemin Ste-Foy, Local J0 - 01, Quebec City, QC, G1S 4L8, Canada.
BMC medical genomics
|April 16, 2025
概括
基因组研究缺乏多样性,影响治疗创新. 研究人员建议解决殖民实践和协调人口描述符,以改善代表性不足的群体参与.
科学领域:
- 基因组学就是基因组学.
- 生物伦理学生物伦理学
- 公共卫生 公共卫生
背景情况:
- 基因组数据的有限多样性阻碍了对遗传特征,疾病和治疗反应的理解.
- 不准确的基因组数据可能会导致代表性不足的人群的有害治疗结果.
- 在基因组研究中不一致地使用人口描述符,引发了伦理和科学方面的担忧.
研究的目的:
- 探索影响少数群体参与基因组研究的社会和上下文因素.
- 从经验丰富的基因组研究人员的角度了解这些因素.
主要方法:
- 进行了13次半结构化采访,对加拿大基因组研究人员进行了采访,他们流利地说法语或英语.
- 使用专题分析分析了采访成绩单.
主要成果:
- 研究机构的地理分布和社区的脱节是参与的主要障碍.
- 远离殖民研究实践,让社区参与研究设计至关重要.
- 现有的多样性,公平性和包容性政策是不够的;人口描述符分类影响参与意愿.
结论:
- 研究人员承认低参与率的原因和解决方案,但在人口描述因素方面面临困惑.
- 需要提高教育,共识和对话来协调基因组研究中的人口描述符.
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