选择性基因组检测后的家族交流和级联检测。

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY Journal of Genetic Counseling Pub Date : 2024-05-16 DOI:10.1002/jgc4.1907
Sophia M Adelson, C. L. Blout Zawatsky, M. Hickingbotham, Megan E Bell, Dylan M Platt, Jennifer R Leonhard, Emilie S. Zoltick, Catherine A Hajek, Robert C. Green, Kurt D Christensen
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引用次数: 0

摘要

结果的家属沟通和级联基因检测(CGT)可将基因筛查的益处从患者扩展到其高危亲属。虽然越来越多的医疗系统将基因筛查作为一项选择性临床服务,但关于结果共享的频率以及结果导致CGT的频率的数据却很有限。从 2018 年到 2022 年,桑福德医疗系统向其成年初级保健患者提供了桑福德芯片,这是一种选择性基因组检测,包括筛查美国医学遗传学和基因组学学会推荐的可医学操作的疾病倾向,以披露次要结果。我们分析了至少一年前收到桑福德芯片检测结果的患者报告的有关家族共享结果和 CGT 的数据。在已确定有可采取行动的医学倾向的患者中,94.6%(53/56)的患者报告至少向一位家庭成员透露了他们的检查结果,而在检查结果不明的患者中,46.7%(423/906)的患者透露了他们的检查结果(P < 0.001)。在有可采取行动倾向的患者中,52.2%(12/23)的单基因疾病风险患者和 12.1%(4/33)的携带者患者报告其亲属接受了 CGT。结果表明,虽然在选择性基因组检测中发现单基因风险促使许多高危亲属进行了 CGT,但仍有一些未经检测的高危亲属可能会从未来的 CGT 中受益。研究结果表明,加强遗传咨询、开发工具和资源以鼓励家庭成员进行 CGT,可能会使这一领域受益。
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Familial communication and cascade testing following elective genomic testing.
Familial communication of results and cascade genetic testing (CGT) can extend the benefits of genetic screening beyond the patient to their at-risk relatives. While an increasing number of health systems are offering genetic screening as an elective clinical service, data are limited about how often results are shared and how often results lead to CGT. From 2018 to 2022, the Sanford Health system offered the Sanford Chip, an elective genomic test that included screening for medically actionable predispositions for disease recommended by the American College of Medical Genetics and Genomics for secondary findings disclosure, to its adult primary care patients. We analyzed patient-reported data about familial sharing of results and CGT among patients who received Sanford Chip results at least 1 year previously. Among the patients identified with medically actionable predispositions, 94.6% (53/56) reported disclosing their result to at least one family member, compared with 46.7% (423/906) of patients with uninformative findings (p < 0.001). Of the patients with actionable predispositions, 52.2% (12/23) with a monogenic disease risk and 12.1% (4/33) with a carrier status reported that their relatives underwent CGT. Results suggest that while the identification of monogenic risk during elective genomic testing motivates CGT in many at-risk relatives, there remain untested at-risk relatives who may benefit from future CGT. Findings identify an area that may benefit from increased genetic counseling and the development of tools and resources to encourage CGT for family members.
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来源期刊
Journal of Genetic Counseling
Journal of Genetic Counseling GENETICS & HEREDITY-
CiteScore
3.80
自引率
26.30%
发文量
113
审稿时长
6 months
期刊介绍: The Journal of Genetic Counseling (JOGC), published for the National Society of Genetic Counselors, is a timely, international forum addressing all aspects of the discipline and practice of genetic counseling. The journal focuses on the critical questions and problems that arise at the interface between rapidly advancing technological developments and the concerns of individuals and communities at genetic risk. The publication provides genetic counselors, other clinicians and health educators, laboratory geneticists, bioethicists, legal scholars, social scientists, and other researchers with a premier resource on genetic counseling topics in national, international, and cross-national contexts.
期刊最新文献
The current landscape of clinical exome and genome reanalysis in the U.S. A cross-sectional survey-based exploration of diversity in the admissions committees and student cohorts of genetic counseling programs over time. An analysis of direct-to-consumer genetic testing portals and their communication of health risk and test limitations. Patient perceptions of genetic counselors' role and emotional support needs in adults with Parkinson's disease Clinical genetic counselors' use of people‐ and identity‐first language in regard to patients' identification with disability
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