研究相关基因检测结果的回归和基因歧视问题:不同群体参与基因研究的促进因素和障碍。

IF 1.3 4区 医学 Q4 GENETICS & HEREDITY
Public Health Genomics Pub Date : 2020-01-01 Epub Date: 2020-04-14 DOI:10.1159/000507056
Andrea N Burnett-Hartman, Erica Blum-Barnett, Nikki M Carroll, Sarah D Madrid, Cabell Jonas, Kristen Janes, Monica Alvarado, Ruth Bedoy, Valerie Paolino, Nazneen Aziz, Elizabeth A McGlynn
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引用次数: 14

摘要

背景:大多数遗传学研究缺乏必要的多样性,以确保所有群体都能从遗传研究中受益。目的:探讨基因研究参与的促进因素和障碍。方法:于2017年11月15日至2018年2月28日,对受邀加入Kaiser Permanente (KP)生物库(KP research Bank)的成年会员进行研究和医疗保健遗传学调查。根据人口统计学特征,采用logistic回归计算校正比值比(ORs)和95%置信区间(ci),比较不同结果回归情景下人群参与基因研究的意愿和基因歧视问题。结果:共有57,331名KP成员受邀参与,其中10,369人完成了调查(回复率为18%)。受访者中65%为女性,44%为非西班牙裔白人(NH White), 22%为亚洲/夏威夷原住民或其他太平洋岛民(Asian/PI), 19%为非西班牙裔黑人(NH Black), 16%为西班牙裔。愿意参与基因研究的受访者从没有结果的22%到有健康相关基因结果的87%不等。我们还发现了种族/民族的差异;当没有结果返回时,亚洲/ pi,西班牙裔和NH黑人比NH白人更不愿意参与(p < 0.05)。然而,当结果返回时,参与意愿的差异在新罕布什尔州黑人和西班牙裔人中消失了。遗传歧视问题在亚洲/ pi、西班牙裔和NH黑人中比在NH白人中更为普遍(p < 0.05)。结论:禁止返回结果和不解决基因歧视问题的政策可能会导致基因研究中不同群体的代表性更低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Return of Research-Related Genetic Test Results and Genetic Discrimination Concerns: Facilitators and Barriers of Genetic Research Participation in Diverse Groups.

Background: Most genetics studies lack the diversity necessary to ensure that all groups benefit from genetic research.

Objectives: To explore facilitators and barriers to genetic research participation.

Methods: We conducted a survey on genetics in research and healthcare from November 15, 2017 to February 28, 2018 among adult Kaiser Permanente (KP) members who had been invited to participate in the KP biobank (KP Research Bank). We used logistic regression to calculate adjusted odds ratios (ORs) and 95% confidence intervals (CIs) comparing the willingness to participate in genetic research under different return of results scenarios and genetic discrimination concerns between groups, according to their demographic characteristics.

Results: A total of 57,331 KP members were invited to participate, and 10,369 completed the survey (18% response rate). Respondents were 65% female, 44% non-Hispanic White (NH White), 22% Asian/Native Hawaiian or other Pacific Islander (Asian/PI), 19% non-Hispanic Black (NH Black), and 16% Hispanic. Respondents willing to participate in genetic research ranged from 22% with no results returned to 87% if health-related genetic results were returned. We also found variation by race/ethnicity; when no results were to be returned, Asian/PIs, Hispanics, and NH Blacks were less likely to want to participate than NH Whites (p < 0.05). However, when results were returned, disparities in the willingness to participate disappeared for NH Blacks and Hispanics. Genetic discrimination concerns were more prevalent in Asian/PIs, Hispanics, and NH Blacks than in NH Whites (p < 0.05).

Conclusions: Policies that prohibit the return of results and do not address genetic discrimination concerns may contribute to a greater underrepresentation of diverse groups in genetic research.

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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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