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Knowledge and utilization of genetic testing: Examining correlation to income.

机译:基因检测的知识和利用:检查与收入的相关性。

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摘要

Scientists completed mapping the human genome in April 2003. Since then, the number of genetic tests available to patients and consumers has burgeoned. This revolution has the promise of drastically changing the way that the medical community addresses diseases. However, with the promise of new types of care comes the possibility of exacerbating disparities in healthcare services. If low-income individuals do not have access to, or knowledge of, genetic testing, this could leave them further behind in terms of medical treatment in the future.This paper examines the relationship between an individual's likelihood of hearing of, or taking, a genetic test and his or her income. Specifically, the paper focuses on genetic tests for various types of cancer, which are among the most widely used and scientifically sound genetic tests available. The paper uses logistic regressions with data from the 2005 National Health Interview Survey, including information from the Cancer Module Supplement, an additional set of questions asked only in the 2005 survey. The analysis tests the hypothesis that people with lower incomes will be less likely to have heard of or taken a genetic test for cancer, controlling for demographic variables, such as education, individual medical history, family history of cancer, access to doctors, and personal attitudes about risk.The results indicate that people with higher annual family incomes are more likely than those with lower incomes to be aware of genetic testing. The results, however, find limited evidence of a relationship between income and the likelihood of having taken a genetic test among the subpopulation of people who have heard of genetic testing.In the future, access to genetic testing will likely have large effects on the effectiveness and quality of an individual's medical care. If some portions of the population are not aware of genetic tests they may be left behind. This study suggests that it may be beneficial for policy-makers and consumer advocates to target awareness campaigns towards those portions of the population that are less likely to be aware of genetic testing.
机译:科学家于2003年4月完成了人类基因组图谱的绘制。从那时起,可供患者和消费者使用的基因测试数量迅速增加。这场革命有望彻底改变医学界应对疾病的方式。但是,随着新型医疗服务的出现,可能加剧医疗保健服务之间的差距。如果低收入者无法获得基因检测或他们不了解基因检测,这可能会在将来的医疗方面使他们进一步落后。本文研究了个体听到或接受某种基因检测的可能性之间的关系。基因检测及其收入。具体而言,本文着重于针对各种类型癌症的基因测试,这些测试是最广泛使用且科学上合理的基因测试之一。这篇论文将logistic回归与2005年美国国民健康访问调查中的数据结合使用,其中包括来自癌症模块补充资料中的信息,这是仅在2005年调查中提出的另一组问题。该分析检验了以下假设:收入较低的人不太可能听说过癌症或接受了癌症的基因检测,从而控制了人口统计学变量,例如教育程度,个人病史,癌症家族史,就医机会以及个人结果表明,家庭年收入较高的人比收入较低的人更容易意识到基因检测。然而,研究结果发现,在听说过基因检测的人群中,收入与进行基因检测的可能性之间的关系的证据有限。未来,基因检测的获得可能会对有效性产生重大影响和个人医疗质量。如果人口的某些部分不了解基因检测,他们可能会被抛在后面。这项研究表明,对于决策者和消费者权益倡导者来说,将宣传运动针对不太可能了解基因检测的人群是有益的。

著录项

  • 作者

    Prince, Anya E.;

  • 作者单位

    Georgetown University.;

  • 授予单位 Georgetown University.;
  • 学科 Biology Genetics.Sociology Public and Social Welfare.
  • 学位 M.P.P.
  • 年度 2010
  • 页码 46 p.
  • 总页数 46
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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