3.8 Article

Willingness to participate in genomics research and desire for personal results among underrepresented minority patients: a structured interview study

期刊

JOURNAL OF COMMUNITY GENETICS
卷 4, 期 4, 页码 469-482

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s12687-013-0154-0

关键词

Genomicsresearch; Interest; Interviews; Patients; Personal results

资金

  1. Seed Grant Program of The Charles Bronfman Institute for Personalized Medicine from the National Center for Advancing Translational Sciences, National Institutes of Health [UL1RR029887]
  2. electronic medical records and genomics (eMERGE) network of the National Human Genome Research Institute, National Institutes of Health [U01HG006380]

向作者/读者索取更多资源

Patients from traditionally underrepresented communities need to be involved in discussions around genomics research including attitudes towards participation and receiving personal results. Structured interviews, including openended and closed-ended questions, were conducted with 205 patients in an inner-city hospital outpatient clinic: 48 % of participants self-identified as Black or African American, 29 % Hispanic, 10 % White; 49 % had an annual household income of <$20,000. When the potential for personal results to be returned was not mentioned, 82 % of participants were willing to participate in genomics research. Reasons for willingness fell into four themes: altruism; benefit to family members; personal health benefit; personal curiosity and improving understanding. Reasons for being unwilling fell into five themes: negative perception of research; not personally relevant; negative feelings about procedures (e.g., blood draws); practical barriers; and fear of results. Participants were more likely to report that they would participate in genomics research if personal results were offered than if they were not offered (89 vs. 62 % respectively, p<0.001). Participants were more interested in receiving personal genomic risk results for cancer, heart disease and type 2 diabetes than obesity (89, 89, 91, 80 % respectively, all p<0.001). The only characteristic consistently associated with interest in receiving personal results was disease-specific worry. There was considerable willingness to participate in and desire for personal results from genomics research in this sample of predominantly low-income, Hispanic and African American patients. When returning results is not practical, or even when it is, alternatively or additionally providing generic information about genomics and health may also be a valuable commodity to underrepresented minority and other populations considering participating in genomics research.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据