The role of disease characteristics in the ethical debate on personal genome testing

被引:23
作者
Bunnik, Eline M. [1 ]
Schermer, Maartje H. N. [1 ]
Janssens, A. Cecile J. W. [2 ]
机构
[1] Erasmus Univ, Med Ctr, Dept Med Eth & Philosophy Med, NL-3015 GE Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Dept Epidemiol, NL-3015 GE Rotterdam, Netherlands
关键词
RISK; INFORMATION; CHILDREN; ILLNESS; OBESITY; IMPACT; LEGAL;
D O I
10.1186/1755-8794-5-4
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Background: Companies are currently marketing personal genome tests directly-to-consumer that provide genetic susceptibility testing for a range of multifactorial diseases simultaneously. As these tests comprise multiple risk analyses for multiple diseases, they may be difficult to evaluate. Insight into morally relevant differences between diseases will assist researchers, healthcare professionals, policy-makers and other stakeholders in the ethical evaluation of personal genome tests. Discussion: In this paper, we identify and discuss four disease characteristics - severity, actionability, age of onset, and the somatic/psychiatric nature of disease - and show how these lead to specific ethical issues. By way of illustration, we apply this framework to genetic susceptibility testing for three diseases: type 2 diabetes, age-related macular degeneration and clinical depression. For these three diseases, we point out the ethical issues that are relevant to the question whether it is morally justifiable to offer genetic susceptibility testing to adults or to children or minors, and on what conditions. Summary: We conclude that the ethical evaluation of personal genome tests is challenging, for the ethical issues differ with the diseases tested for. An understanding of the ethical significance of disease characteristics will improve the ethical, legal and societal debate on personal genome testing.
引用
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页数:9
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