Suppr超能文献

比较参与基因组研究存储库的青少年及其家长对基因组隐私和数据共享的态度。

Comparing Attitudes About Genomic Privacy and Data Sharing in Adolescents and Parents of Children Enrolled in a Genomic Research Repository.

机构信息

Genomic Medicine Center, Children's Mercy Kansas City, Kansas City, MO, USA.

School of Medicine, University of Missouri Kansas City, Kansas City, MO, USA.

出版信息

AJOB Empir Bioeth. 2024;15(1):33-40. doi: 10.1080/23294515.2023.2232780. Epub 2023 Jul 24.

Abstract

BACKGROUND

Sharing of genomic data aims to make efficient use of limited resources, which may be particularly valuable in rare disease research. Adult research participants and parents of pediatric research participants have shown support for data sharing with protections, but little is known about adolescent attitudes on genomic privacy and data sharing.

METHODS

In-depth interviews were conducted with 10 adolescents and 18 parents of children enrolled in a pediatric genomic research repository. Interview transcripts were analyzed for themes on attitudes toward genomic privacy, restricted-access data sharing, and open-access data sharing. Findings in adolescent and parent participants were compared and contrasted.

RESULTS

No adolescents endorsed privacy concerns for restricted-access data sharing. Both adolescents and parents saw value in data sharing for reaching the goals of research and discussed trust in institutions and researchers to protect their data and use it as intended. Adolescents were more likely than parents to accept open-access data sharing, including after risks were discussed.

CONCLUSIONS

In this exploratory study, adolescents and parents enrolled in a genomic research repository shared many attitudes about genomic data sharing, but adolescents were less concerned about privacy and more agreeable toward open-access data sharing. Future research is needed to investigate this hypothesis in expanded populations and settings, and to clarify whether adolescent attitudes change with age and experiences.

摘要

背景

基因组数据共享旨在有效利用有限的资源,这在罕见病研究中可能特别有价值。成年研究参与者和儿科研究参与者的父母都表示支持在保护措施下共享数据,但对于青少年对基因组隐私和数据共享的态度,我们知之甚少。

方法

对参加儿科基因组研究存储库的 10 名青少年和 18 名儿童父母进行了深入访谈。对访谈记录进行了主题分析,内容涉及对基因组隐私的态度、限制访问数据共享和开放访问数据共享。比较和对比了青少年和家长参与者的发现。

结果

没有青少年对限制访问数据共享表示隐私问题。青少年和父母都认为数据共享对于实现研究目标具有价值,并讨论了对机构和研究人员保护数据并按预期使用数据的信任。与父母相比,青少年更有可能接受开放访问数据共享,包括在讨论了风险之后。

结论

在这项探索性研究中,参加基因组研究存储库的青少年和父母对基因组数据共享有许多共同的态度,但青少年对隐私问题的担忧较少,对开放访问数据共享更持赞成态度。未来需要在更广泛的人群和环境中进行研究,以调查这一假设,并澄清青少年的态度是否会随着年龄和经验的变化而变化。

相似文献

2
Pediatric data sharing in genomic research: attitudes and preferences of parents.
Pediatrics. 2014 Apr;133(4):690-7. doi: 10.1542/peds.2013-1592. Epub 2014 Mar 10.
3
Context matters in genomic data sharing: a qualitative investigation into responses from the Australian public.
BMC Med Genomics. 2023 Apr 1;15(Suppl 3):275. doi: 10.1186/s12920-023-01452-8.
4
Sharing longitudinal, non-biological birth cohort data: a cross-sectional analysis of parent consent preferences.
BMC Med Inform Decis Mak. 2018 Nov 12;18(1):97. doi: 10.1186/s12911-018-0683-x.
5
Australian Attitudes Towards Waivers of Consent Within the Context of Genomic Data Sharing.
J Empir Res Hum Res Ethics. 2024 Jul;19(3):113-123. doi: 10.1177/15562646241261848.
6
Public perspectives regarding data-sharing practices in genomics research.
Public Health Genomics. 2011;14(6):319-24. doi: 10.1159/000324705. Epub 2011 Mar 24.
7
Ethical, Legal, and Social Issues (ELSI) of Responsible Data Sharing Involving Children in Genomics: A Systematic Literature Review of Reasons.
AJOB Empir Bioeth. 2020 Oct-Dec;11(4):233-245. doi: 10.1080/23294515.2020.1818875. Epub 2020 Sep 25.
8
Public attitudes towards genomic data sharing: results from a provincial online survey in Canada.
BMC Med Ethics. 2023 Oct 7;24(1):81. doi: 10.1186/s12910-023-00967-0.
9
Parent perspectives on privacy and governance for a pediatric repository of non-biological, research data.
J Empir Res Hum Res Ethics. 2015 Feb;10(1):88-99. doi: 10.1177/1556264614564970. Epub 2014 Dec 31.

本文引用的文献

1
National Human Genome Research Institute Genomic Data Science Analysis, Visualization, and Informatics Lab-Space: Reaching out to Clinicians.
Circ Genom Precis Med. 2023 Jun;16(3):275-276. doi: 10.1161/CIRCGEN.122.003936. Epub 2023 Apr 4.
2
Data sharing in the age of predictive psychiatry: an adolescent perspective.
Evid Based Ment Health. 2022 May;25(2):69-76. doi: 10.1136/ebmental-2021-300329. Epub 2022 Mar 28.
3
Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey.
AJOB Empir Bioeth. 2018 Jul-Sep;9(3):128-142. doi: 10.1080/23294515.2018.1505783. Epub 2018 Sep 21.
5
De-identified genomic data sharing: the research participant perspective.
J Community Genet. 2017 Jul;8(3):173-181. doi: 10.1007/s12687-017-0300-1. Epub 2017 Apr 5.
7
Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
Am J Hum Genet. 2017 Mar 2;100(3):414-427. doi: 10.1016/j.ajhg.2017.01.021. Epub 2017 Feb 9.
8
A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.
Genet Med. 2016 Jul;18(7):663-71. doi: 10.1038/gim.2015.138. Epub 2015 Nov 19.
9
Pediatric data sharing in genomic research: attitudes and preferences of parents.
Pediatrics. 2014 Apr;133(4):690-7. doi: 10.1542/peds.2013-1592. Epub 2014 Mar 10.
10
Research participants' attitudes towards the confidentiality of genomic sequence information.
Eur J Hum Genet. 2014 Aug;22(8):964-8. doi: 10.1038/ejhg.2013.276. Epub 2013 Nov 27.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验