"真相不应被掩盖":通过基因家谱数据库发现 NPE 的个人经验和建议。

IF 6.6 1区 医学 Q1 GENETICS & HEREDITY
Olivia Schuman , Caroline Beit , Jill Oliver Robinson , Whitney Bash Brooks , Amy L. McGuire , Christi Guerrini
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引用次数: 0

摘要

目的:在直接面向消费者(DTC)的基因检测和基因亲属查找(GRF)服务的推动下,一些基因家谱数据库的参与者发现了 "非预期父母"(NPE)。为了更好地了解这一现象的经历,我们对一大批 GRF 服务用户进行了调查,了解他们在发现 NPE 后的经历:我们使用主题分析法,分析了一批 GRF 用户(n=646)对开放式调查项目的回答,以了解这些经历以及他们对 DTC 基因检测公司和其他 GRF 用户的建议:我们发现,个人在发现 NPE 时既有积极的情感体验,也有消极的情感体验。积极方面包括加深对自我的了解、与新的家庭成员建立联系以及发现问题的答案。消极方面包括被新的遗传亲属排斥、无法从已经去世的亲属那里寻求答案,以及家庭关系受损,尤其是与母亲的关系。对许多参与者来说,发现基因后所面临的挑战是值得的,因为真相已经揭开。也许值得注意的是,一些参与者建议提供 DTC 基因检测服务的公司加强发现前的警告和发现后的支持:GRF 服务是家族研究和家谱的有力工具。尽管在发现 NPE 时可能会产生一些积极和有价值的体验,但 GRF 用户仍有可能在没有足够支持的情况下应对这种可能改变生活的体验。本研究的参与者建议 DTC 基因检测公司提供更多资源,帮助用户预测和处理 NPE 发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
“The truth should not be hidden”: Experiences and recommendations of individuals making NPE discoveries through genetic genealogy databases

Purpose

Fueled by direct-to-consumer (DTC) genetic testing and genetic-relative finder services, some participants in genetic genealogy databases are making “not parent expected” (NPE) discoveries. To better understand experiences of this phenomenon, we surveyed a large cohort of users of genetic relative finder (GRF) services concerning their experiences after an NPE discovery.

Methods

Using thematic analysis, we analyzed responses from a cohort of GRF users (n = 646) to open-ended survey items to understand these experiences and their recommendations for DTC genetic testing companies and other GRF users.

Results

We found that individuals had both positive and negative emotional experiences related to the NPE discovery. Positive aspects included deeper self-understanding, connecting with new family members, and uncovering answers to questions. Negative aspects included rejection by new genetic relatives, inability to seek answers from relatives who had already died, and impairment of family relationships, especially with mothers. For many participants, the challenges after the discovery nevertheless felt worthwhile because the truth was uncovered. Perhaps notably, some participants suggested enhanced warnings prediscovery and improved support after discovery from companies who provide DTC genetic testing services.

Conclusion

GRF services are powerful tools for family research and genealogy. Despite some possible positive and worthwhile experiences arising from making an NPE discovery, GRF users risk dealing with this potentially life-altering experience without adequate support. Participants in this study recommended an increase in resources from DTC genetic testing companies that could help users anticipate and navigate an NPE discovery.

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来源期刊
Genetics in Medicine
Genetics in Medicine 医学-遗传学
CiteScore
15.20
自引率
6.80%
发文量
857
审稿时长
1.3 weeks
期刊介绍: Genetics in Medicine (GIM) is the official journal of the American College of Medical Genetics and Genomics. The journal''s mission is to enhance the knowledge, understanding, and practice of medical genetics and genomics through publications in clinical and laboratory genetics and genomics, including ethical, legal, and social issues as well as public health. GIM encourages research that combats racism, includes diverse populations and is written by authors from diverse and underrepresented backgrounds.
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