Refining a Multifaceted Model of Perceived Utility of Genomic Sequencing Results.

IF 1.3 4区 医学 Q4 GENETICS & HEREDITY Public Health Genomics Pub Date : 2023-01-01 Epub Date: 2023-08-22 DOI:10.1159/000531782
Devan M Duenas, Leslie Riddle, Claudia Guerra, Mikaella Caruncho, Hannah Lewis, Kathryn M Porter, Stephanie A Kraft, Katherine P Anderson, Barbara Biesecker, Marian J Gilmore, Jamilyn M Zepp, Michael C Leo, Benjamin S Wilfond, Galen Joseph
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Abstract

Introduction: Research on the perceived utility of genomic sequencing has focused primarily on pediatric populations and on individuals and families with rare genetic diseases. Here, we evaluate how well a multifaceted perceived utility model developed with these populations applies to a diverse, adult population aged 18-49 at risk for hereditary cancer and propose new considerations for the model.

Methods: Participants received clinical genomic sequencing in the Cancer Health Assessments Reaching Many (CHARM) study. Semi-structured qualitative interviews were conducted with a subset of participants at 1 and 6 months after results disclosure. We used an approach influenced by grounded theory to examine perceptions of the utility of genomic sequencing and analyzed how utility in CHARM mapped to the published multifaceted perceived utility model, noting which domains were represented or absent and which were most salient to our population.

Results: Participants' discussions of utility often involved multiple domains and revealed the variety of ways in which receiving sequencing results can impact one's life. Results demonstrated that an individual's perception of utility can change over the life course when sequenced at a relatively young age and may be influenced by the resources available to them to act on the results.

Conclusion: Our findings demonstrate the relevance of a multifaceted perceived utility model for a diverse adult population at risk for hereditary cancer. We identified refinements that could make the model more robust, including emphasizing the overlapping nature of the domains and the importance of life stage and personal resources to the perception of utility.

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完善基因组测序结果的感知效用的多方面模型。
引言:关于基因组测序的实用性的研究主要集中在儿科人群以及患有罕见遗传病的个人和家庭。在此,我们评估了利用这些人群开发的多方面感知实用新型在多大程度上适用于18-49岁有遗传性癌症风险的多样化成年人群,并提出了该模型的新考虑因素。方法:参与者在癌症健康评估达到许多(CHARM)研究中接受临床基因组测序。在结果披露后的一个月和六个月,对一部分参与者进行了半结构化的定性访谈。我们使用了一种受基础理论影响的方法来检验对基因组测序效用的感知,并分析了CHARM中的效用如何映射到已发表的多方面感知效用模型,注意哪些领域被代表或不存在,哪些领域对我们的人群最为突出。结果:参与者对效用的讨论通常涉及多个领域,并揭示了接收测序结果对一个人生活的各种影响。研究结果表明,当在相对年轻的时候进行测序时,个体的效用感知可能会在整个生命过程中发生变化,并可能受到可用于对结果采取行动的资源的影响。讨论/结论:我们的研究结果证明了多方面感知实用新型与遗传性癌症风险的不同成年人群的相关性。我们确定了可以使模型更加稳健的改进,包括强调领域的重叠性质,以及人生阶段和个人资源对效用感知的重要性。
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来源期刊
Public Health Genomics
Public Health Genomics 医学-公共卫生、环境卫生与职业卫生
CiteScore
2.90
自引率
0.00%
发文量
14
审稿时长
>12 weeks
期刊介绍: ''Public Health Genomics'' is the leading international journal focusing on the timely translation of genome-based knowledge and technologies into public health, health policies, and healthcare as a whole. This peer-reviewed journal is a bimonthly forum featuring original papers, reviews, short communications, and policy statements. It is supplemented by topic-specific issues providing a comprehensive, holistic and ''all-inclusive'' picture of the chosen subject. Multidisciplinary in scope, it combines theoretical and empirical work from a range of disciplines, notably public health, molecular and medical sciences, the humanities and social sciences. In so doing, it also takes into account rapid scientific advances from fields such as systems biology, microbiomics, epigenomics or information and communication technologies as well as the hight potential of ''big data'' for public health.
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