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Impact of Direct to Consumer Genetic Testing

Impact of Direct to Consumer Genetic Testing
直接对消费者基因检测的影响
批准号:
7987948
负责人:
Robert C. Green
金额:
$41.1万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-26 至 2011-04-01

项目摘要

项目成果

Robert C. Green的其他基金

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中文摘要
翻译
描述(由申请人提供):快速识别常见复杂疾病的遗传风险因素为公共卫生带来了巨大的机遇和挑战。遗传信息越来越多地被用作商业努力的一部分,包括直接面向消费者(DTC)的基因检测,向消费者提供常见疾病的风险信息。很少收集到经验数据来了解DTC测试消费者的特征、心理、行为和健康影响以及与DTC服务相关的伦理、法律和社会问题。在拟议的研究中,我们将调查提供DTC基因检测的两家领先的美国公司(23andMe和Navigenics)的用户,了解他们对常见疾病基因检测的反应,包括心脏病、糖尿病、阿尔茨海默病、关节炎、乳腺癌、结肠癌、肺癌和前列腺癌。每家公司现在都有成千上万的客户,每家公司都预计未来几年将有广泛的销售。每个人都同意允许我们的小组使用第三方数据收集和分析程序对消费者进行调查,这将使我们能够独立考虑这种形式的DTC测试的好处和风险。这些公司还同意提供基因检测信息(在得到受访者同意的情况下)用于分析。在收到基因检测结果之前,我们将通过互联网对1000名消费者(每家公司500名)进行调查,并在收到结果后的1-2周和6个月对该样本进行再次调查。为了开展拟议的研究,我们组建了一个跨学科的专家团队,他们的背景包括医学、基因检测政策与实践、健康传播、遗传咨询、健康心理学、卫生法、生物伦理学和网络调查设计。许多团队成员都曾合作过elsi资助的相关研究。我们的目标如下:1)描述谁寻求基因检测及其原因,收集人口统计学信息,寻求检测的动机,以及对遗传学的理解;2)描述DTC基因检测的影响,包括心理影响、风险认知和理解以及服务的个人效用;3)评估消费者在健康行为、保险变更、信息寻求以及与家庭和医疗保健提供者的沟通等方面对其遗传信息的使用情况。这项研究将产生的结果可转化为指导这一迅速崛起领域的实践和政策的建议。
英文摘要
DESCRIPTION (provided by applicant): The rapid identification of genetic risk factors for common, complex diseases poses great opportunities and challenges for public health. Genetic information is increasingly being utilized as part of commercial efforts, including direct-to-consumer (DTC) genetic testing to provide risk information on common diseases to consumers. Very few empirical data have been gathered to understand the characteristics of DTC test consumers, the psychological, behavioral and health impact, and the ethical, legal and social issues associated with DTC services. In the proposed research, we will survey users of the two leading US companies providing DTC genetic testing (23andMe and Navigenics) regarding their response to genetic tests for common diseases of interest, including heart disease, diabetes, Alzheimer's disease, arthritis, and breast, colon, lung and prostate cancers. Each company now has thousands of customers and each anticipates extensive sales in coming years. Each has agreed to allow our group to survey consumers using third-party data collection and analysis procedures that will enable an independent consideration of the benefits and risks of DTC testing in this format. The companies have also agreed to provide genetic test information (with respondents' permission) for analyses. A total of 1000 consumers (500 from each company) will be surveyed via the Internet before receipt of genetic test results, and we will survey this sample again at 1-2 weeks and six months following receipt of results. To carry out the proposed research, we have assembled an interdisciplinary team of experts with backgrounds in medicine, genetic testing policy and practice, health communication, genetic counseling, health psychology, health law, bioethics and web survey design. Many team members have collaborated on prior, related ELSI-funded research. Our aims are as follows: 1) to describe who seeks genetic testing and why, collecting information on demographics, motivations for seeking testing, and understanding of genetics; 2) to describe the impact of DTC genetic testing, including psychological impact, risk perceptions and comprehension, and personal utility of services; and 3) to assess what consumers do with their genetic information in the domains of health behaviors, insurance changes, information seeking, and communication with family and health care providers. This study will produce results that can be translated into recommendations to guide practice and policy in this rapidly emerging area. PUBLIC HEALTH RELEVANCE: Genetic information is increasingly being utilized as part of commercial efforts, including direct-to-consumer (DTC) genetic testing to provide risk information on common diseases to consumers. We will survey customers of the two leading DTC genetic test services in the U.S., using independent third party data collection and analysis to provide data on who is ordering these tests and why, and what its benefits and risks may be. This study will produce results that can be translated into recommendations to guide practice and policy in this rapidly emerging area.
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Implementation of Whole Genome Sequencing as Screening in a Diverse Cohort of Healthy Infants
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    10652609
  • 项目类别:
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  • 财政年份:
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  • 负责人:
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  • 依托单位:
Implementation of Whole Genome Sequencing as Screening in a Diverse Cohort of Healthy Infants
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Experiences and Outcomes in Early Adopters of Predispositional Sequencing
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Experiences and Outcomes in Early Adopters of Predispositional Sequencing
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  • 项目类别:
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    $80.0万
  • 财政年份:
    2018
  • 负责人:
    Robert C. Green
  • 依托单位:
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