研究生物库参与者对遗传特异性和健康记录保密性的态度。

IF 1.5 Q4 GENETICS & HEREDITY
Journal of Community Genetics Pub Date : 2024-06-01 Epub Date: 2024-03-05 DOI:10.1007/s12687-024-00704-z
Victoria Dortenzio, Rosamond Rhodes, Amanda Merkelson, Hetanshi Naik
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引用次数: 0

摘要

了解人们对基因特殊性和保密性的态度对于指导有关对电子健康记录(EHR)中存储的基因/基因组信息进行特殊保护的政策非常重要。本研究的目的是确定生物库参与者对基因特殊性和保密性的态度,以及这些态度是否与他们对返还基因结果的偏好有关。研究人员向曾经注册过 BioMe 生物库项目、拥有电子病历和电子邮件地址的患者发放了一份在线问卷。大多数参与者在回答涉及使用遗传信息和其他类型健康信息的情况时,表示了类似程度的担忧,这表明参与者希望遗传数据得到与其他类型敏感健康信息类似的保护,尤其是心理健康和家族病史记录。在 829 位受访者中,尽管他们对遗传信息和其他健康信息保密性的关注程度相似,但在 直接询问时,大多数受访者持遗传例外论者的观点。那些有文件证明他们希望遗传结果被归还的受访者和那些没有文件证明的受访者在遗传特 殊主义观点上没有差异。值得注意的是,对于许多参与者来说,他们回忆起的偏好与其记录的偏好并不一致。大多数生物银行参与者最担心的是基因、心理健康和家族史信息会失去保密性,这表明某些类型的健康信息比其他信息更 "敏感"。这些发现表明,向参与生物库研究的人保证其 "敏感 "健康信息的保密性非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Research biobank participants attitudes towards genetic exceptionalism and health record confidentiality.

Understanding attitudes towards genetic exceptionalism and confidentiality is important in guiding policies regarding special protections for genetic/genomic information stored in electronic health records (EHR). The goals of this study were to determine biobank participants' attitudes towards genetic exceptionalism and confidentiality and whether those attitudes are related to their preference for return of genetic results. An online questionnaire was distributed to patients with an EHR and email address who had previously enrolled in the BioMe Biobank program. Most participants responded with similar levels of concern in scenarios involving the use of genetic information and other types of health information, suggesting that participants want similar protections for genetic data as other types of sensitive health information, particularly mental health and family history records. Of the 829 respondents, the majority had genetic exceptionalist views when directly asked, even though their concerns about confidentiality were similar for their genetic information and other health information. There were no differences in genetic exceptionalist views between those who had a documented preference to have genetic results returned and those who did not. Notably, for many participants, their recall of preference did not align with their documented preference. The majority of biobank participants were most anxious about the loss of confidentiality for genetic, mental health, and family history information, indicating that certain types of health information are considered more "sensitive" than others. These findings suggest the importance of assuring people participating in biobank research that the confidentiality of their "sensitive" health information is secured.

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来源期刊
Journal of Community Genetics
Journal of Community Genetics GENETICS & HEREDITY-
CiteScore
3.30
自引率
5.30%
发文量
54
期刊介绍: The Journal of Community Genetics is an international forum for research in the ever-expanding field of community genetics, the art and science of applying medical genetics to human communities for the benefit of their individuals. Community genetics comprises all activities which identify persons at increased genetic risk and has an interest in assessing this risk, in order to enable those at risk to make informed decisions. Community genetics services thus encompass such activities as genetic screening, registration of genetic conditions in the population, routine preconceptional and prenatal genetic consultations, public education on genetic issues, and public debate on related ethical issues. The Journal of Community Genetics has a multidisciplinary scope. It covers medical genetics, epidemiology, genetics in primary care, public health aspects of genetics, and ethical, legal, social and economic issues. Its intention is to serve as a forum for community genetics worldwide, with a focus on low- and middle-income countries. The journal features original research papers, reviews, short communications, program reports, news, and correspondence. Program reports describe illustrative projects in the field of community genetics, e.g., design and progress of an educational program or the protocol and achievement of a gene bank. Case reports describing individual patients are not accepted.
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