Department of Pediatrics, University of Washington, Seattle, WA 98195, USA.
Am J Med Genet A. 2013 May;161A(5):1064-72. doi: 10.1002/ajmg.a.35914.
Exome sequencing and whole genome sequencing (ES/WGS) present patients and research participants with the opportunity to benefit from a broad scope of genetic results of clinical and personal utility. Yet, this potential for benefit also risks disenfranchising populations such as African Americans (AAs) that are already underrepresented in genetic research and utilize genetic tests at lower rates than other populations. Understanding a diverse range of perspectives on consenting for ES/WGS and receiving ES/WGS results is necessary to ensure parity in genomic health care and research. We conducted a series of 13 focus groups (n = 76) to investigate if and how attitudes toward participation in ES/WGS research and return of results from ES/WGS differ between self-described AAs and non-AAs. The majority of both AAs and non-AAs were willing to participate in WGS studies and receive individual genetic results, but the fraction not interested in either was higher in AAs. This is due in part to different expectations of health benefits from ES/WGS and how results should be managed. Our results underscore the need to develop and test culturally tailored strategies for returning ES/WGS results to AAs.
外显子组测序和全基因组测序 (ES/WGS) 为患者和研究参与者提供了从广泛的临床和个人有用的遗传结果中受益的机会。然而,这种受益的潜力也有可能使非裔美国人(AA)等已经在遗传研究中代表性不足的人群失去权利,他们使用基因检测的比例低于其他人群。了解对 ES/WGS 同意和接收 ES/WGS 结果的不同观点对于确保基因组医疗保健和研究的平等性是必要的。我们进行了一系列 13 个焦点小组(n = 76)的研究,以调查自我描述的 AA 和非 AA 之间对参与 ES/WGS 研究和返回 ES/WGS 结果的态度是否以及如何不同。大多数 AA 和非 AA 都愿意参与 WGS 研究并接收个人遗传结果,但对两者都不感兴趣的比例在 AA 中更高。这部分是由于对 ES/WGS 的健康益处和结果应如何管理的不同期望。我们的研究结果强调了为 AA 返还 ES/WGS 结果制定和测试文化适应策略的必要性。