Lowery Jan T, Axell Lisen, Ku Lisa, Todd Emily B, Kao Dave, Rafaels Nick, Taylor Matt R G, Kudron Elizabeth, Wicks Stephen, Jirikowic Jean, Shalowitz Elise, Crooks Kristy R
Colorado Center for Personalized Medicine, Anschutz Medical Campus, Aurora, CO.
Colorado School of Public Health, Aurora, CO.
Genet Med Open. 2024 May 18;2:101852. doi: 10.1016/j.gimo.2024.101852. eCollection 2024.
To describe our process for returning genetic results to participants in the Colorado Center for Personalized Medicine biobank.
Enrollment in the biobank is open to all adult UCHealth patients. Participants who provided a sample that was genotyped and signed the proper consent were eligible to receive results. Genetic data were generated using a custom genotyping array and confirmed via Sanger sequencing. We used 2 models for returning results and conducted interviews with participants to assess satisfaction with our process, follow-up care, and family communication.
As of July 2022, 73,313 participants had provided a sample and proper consent. Of these, 10,489 samples were genotyped, 137 (1.3%) had initial results, and 62 were confirmed and eligible for return. We returned results to 51 participants, 33% for cardiac risk, 31% cancer, 15% familial hypercholesterolemia, and 21% for other conditions (11 participants refused or did not respond). Less than half of participants had a relevant family history. The majority of participants were glad to receive results and satisfied with our process.
Although array-based genotyping has known limitations that reduce its accuracy, we were able to identify persons with underlying genetic risk who were previously unaware. It is important to establish a process for returning results that follows clinical guidelines, protects participant autonomy, and is amenable to all participants.
描述我们向科罗拉多个性化医学生物样本库参与者反馈基因检测结果的流程。
该生物样本库向所有成年UCHealth患者开放招募。提供了经基因分型的样本并签署了适当知情同意书的参与者有资格获得检测结果。基因数据通过定制基因分型阵列生成,并经桑格测序确认。我们采用两种模式反馈结果,并对参与者进行访谈,以评估他们对我们的流程、后续护理及家庭沟通的满意度。
截至2022年7月,73313名参与者提供了样本并签署了适当知情同意书。其中,10489份样本进行了基因分型,137份(1.3%)有初步结果,62份经确认且符合结果反馈条件。我们向51名参与者反馈了结果,其中33%为心脏疾病风险,31%为癌症,15%为家族性高胆固醇血症,21%为其他疾病(11名参与者拒绝或未回应)。不到一半的参与者有相关家族病史。大多数参与者很高兴收到结果,并对我们的流程感到满意。
尽管基于阵列的基因分型存在已知局限性,会降低其准确性,但我们仍能够识别出此前未意识到自身存在潜在遗传风险的人群。建立一个遵循临床指南、保护参与者自主权且适用于所有参与者的结果反馈流程非常重要。