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首页> 外文期刊>Journal of Community Genetics >Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study
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Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study

机译:种族和种族多样化生物库参与者参与和遗传信息需求的原因:焦点小组研究

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摘要

In order for DNA biobanks to be a valuable reservoir of genetic information, large numbers of participants from all racial and ethnic backgrounds need to be recruited. This study explored reasons for participating in a new biobank among primarily Hispanic and African American individuals, as well as their general attitudes towards genetic research, and their views on obtaining genetic tests. Focus groups were conducted with Mount Sinai Biobank participants recruited from predominantly lower income, minority communities. The topic guide included questions on The Mount Sinai Biobank, genetic research, and genetic testing. All focus groups were audio recorded, transcribed, and analyzed using thematic analysis. The six focus groups comprised 43 participants: 39 females and four males, aged 27–76 years, with a median household income category of $20,000–$39,999. Twenty-one participants were Hispanic, 20 African American, one Asian, and one White. Participants’ reasons for participating in the biobank included altruism, personal and family benefit, and general curiosity. Although there was evidence of conflation between genetic research and genetic testing, most participants held positive views of genetic research and expressed interest in receiving personal genetic test results. Participants wanted to learn more about genetic research and suggested various venues such as health fairs for disseminating information. Participation in biobanks by racial and ethnic minorities is apparently driven by altruism, and desire for personal or collective health benefits. Participants had generally positive attitudes, limited understanding of genetics and genetic research, and made useful suggestions regarding information dissemination mechanisms.
机译:为了使DNA生物库成为有价值的遗传信息库,需要招募来自各个种族和种族背景的大量参与者。这项研究探讨了主要在西班牙裔和非裔美国人中参加新生物库的原因,以及他们对基因研究的一般态度,以及他们对获得基因检测的看法。焦点小组是与西奈山生物银行的参与者进行的,这些参与者是从收入较低的少数族裔社区招募的。主题指南包括有关西奈山生物库,遗传研究和基因检测的问题。所有专题小组都进行了录音,转录和主题分析。六个焦点小组由43位参与者组成:39位女性和4位男性,年龄在27-76岁之间,家庭收入中位数为20,000-39,999美元。 21名参与者是西班牙裔,20名非裔美国人,1名亚裔和1名白人。参与者参加生物库的原因包括利他主义,个人和家庭利益以及人们的好奇心。尽管有证据表明基因研究和基因检测之间存在混淆,但大多数参与者对基因研究持积极态度,并表示有兴趣获得个人基因检测结果。参与者希望了解有关基因研究的更多信息,并建议在各种场所(例如健康博览会)进行信息传播。种族和少数族裔人士参与生物银行显然是由利他主义以及对个人或集体健康利益的渴望驱动的。与会者普遍持积极态度,对遗传学和遗传研究的了解有限,并对信息传播机制提出了有益的建议。

著录项

  • 来源
    《Journal of Community Genetics》 |2011年第3期|p.153-163|共11页
  • 作者单位

    Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine, 1428 Madison Avenue, Box 1497, New York, NY, 10029, USA;

    Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine, 1428 Madison Avenue, Box 1497, New York, NY, 10029, USA;

    Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine, 1428 Madison Avenue, Box 1497, New York, NY, 10029, USA;

    Department of Urology, Mount Sinai School of Medicine, New York, NY, USA;

    Department of Nursing, Mount Sinai School of Medicine, New York, NY, USA;

    Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine, 1428 Madison Avenue, Box 1497, New York, NY, 10029, USA;

    Department of Health Evidence and Policy, Mount Sinai School of Medicine, New York, NY, USA;

    Department of Preventive Medicine, Mount Sinai School of Medicine, New York, NY, USA;

    Department of Health Evidence and Policy,;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    African American; DNA biobank; Focus groups; Hispanics; Motives;

    机译:非裔美国人;DNA生物库;重点人群;西班牙裔;动机;

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