“给我家人的未来礼物”:对参与基因研究的态度

IF 1.3 4区 医学 Q4 GENETICS & HEREDITY
Sarah D Madrid, Erica Blum-Barnett, Amy A Lemke, Vivian Pan, Valerie Paolino, Elizabeth A McGlynn, Andrea N Burnett-Hartman
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引用次数: 0

摘要

背景:需要广泛参与基因研究,以促进疾病治疗和预防的公平进展。目的:本研究的目的是评估参与基因研究的动机和关注点。方法:于2017-2018年冬季向来自美国7个地区的57331名Kaiser Permanente (KP)成年会员发送研究和医疗保健遗传学调查,以评估他们对医疗保健和研究中基因检测的态度。该调查包括一个开放式问题,即成员为什么愿意或不愿意参与基因研究。对这个问题的开放文本回答在定性分析软件Dedoose中进行编码,并使用主题分析方法进行分析。代码摘要按照主要主题、次要主题和典型引用进行组织。结果:在10,369名完成调查的参与者中,2,645名(25%)提供了评论,描述了他们愿意或不愿意参与涉及基因检测的研究的原因。提供文本评论的受访者中有64%为女性,49%为非西班牙裔白人,17%为亚洲/太平洋岛民,20%为西班牙裔,14%为NH黑人。确定的主要主题是:(1)利他主义;(2)决策和规划;(三)数据使用;(4)数据安全。这些主题在每个种族和族裔群体中都是一致的。结论:为了促进基因研究的广泛参与,重要的是招聘材料要解决基因研究参与的主要动机,包括利他主义和可能将结果用于个人决策。研究材料还应解决对可能滥用遗传信息的担忧以及对潜在数据泄露的担忧。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
"A Gift to My Family for Their Future": Attitudes about Genetic Research Participation.

Background: Broad participation in genetic research is needed to promote equitable advances in disease treatment and prevention.

Objectives: The objective of the study was to assess motivations for, and concerns about, genetic research participation.

Methods: The Genetics in Research and Health Care Survey was sent in winter 2017-2018 to 57,331 adult Kaiser Permanente (KP) members from 7 US regions to assess attitudes about genetic testing in health care and research. The survey included an open-ended question on why members would or would not participate in genetic research. Open text responses to this question were coded in the qualitative analysis software Dedoose and analyzed using a thematic analysis approach. Code summaries were organized by major themes, subthemes, and exemplary quotes.

Results: Of the 10,369 participants who completed the survey, 2,645 (25%) provided a comment describing reasons they would or would not participate in research involving genetic testing. Respondents who provided a text comment were 64% female, 49% non-Hispanic (NH) White, 17% Asian/Pacific Islander, 20% Hispanic, and 14% NH Black. The primary themes identified were (1) altruism; (2) decision-making and planning; (3) data use; and (4) data security. These major themes were consistent across each race and ethnic group.

Conclusions: To promote broad participation in genetic research, it is important that recruitment materials address the primary motivators for genetic research participation, including altruism and the potential use of results for personal decision-making. Study materials should also address concerns about possible misuse of genetic information and fears over potential data breaches.

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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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