Where There’s a Web, There’s a Way: Commercial Genetic Testing and the Internet
- 1 April 2003
- journal article
- Published by S. Karger AG in Public Health Genomics
- Vol. 6 (1), 46-57
- https://doi.org/10.1159/000069538
Abstract
The Internet has become a ‘global marketplace’, enabling consumers to purchase health care products and services, including genetic testing, through a variety of national and international sources. A web search for commercial (for-profit) genetic testing companies found 12 with a web presence that were offering adult genetic susceptibility testing, of which 3 offered direct-to-consumer access. In this paper, Canada – with its educated population and universal health care system – will serve as a case study for illustrating the social, ethical and policy issues (e.g., information privacy, just access to health care, product safety, and access to unbiased health information) arising with Internet-based access to commercial genetic testing. Health professionals, policy makers and consumers in all developed nations will be faced with complex technical, social and ethical issues, but without further discussion it will not be possible to determine how best to manage and maximise the benefits of this increased accessibility and choice, while minimising the associated personal and social costs.Keywords
This publication has 15 references indexed in Scilit:
- Risk-Reducing Salpingo-oophorectomy in Women with aBRCA1orBRCA2MutationNew England Journal of Medicine, 2002
- Ethics and genetics: susceptibility testing in the workplace.Journal of Business Ethics, 2002
- Tamoxifen and Breast Cancer Incidence Among Women With Inherited Mutations in BRCA1 and BRCA2JAMA, 2001
- Playing Fair with Consumer Privacy in the Global On-line EnvironmentInformation & Communications Technology Law, 2001
- Harbinger of Hope or Commodity Fetishism: “Re-cognizing” Dementia in an Age of Therapeutic AgentsInternational Psychogeriatrics, 2001
- Misconceptions about the use of genetic tests in populationsThe Lancet, 2001
- Beyond consent: ethical and social issues in genetic testingNature Reviews Genetics, 2001
- Laws Restricting Health Insurers' Use of Genetic Information: Impact on Genetic DiscriminationAmerican Journal of Human Genetics, 2000
- ‘There’s this thing in our family’: predictive testing and the construction of risk for Huntington DiseaseSociology of Health & Illness, 1999
- Are Practicing and Future Physicians Prepared to Obtain Informed Consent? The Case of Genetic Testing forSusceptibility to Breast CancerPublic Health Genomics, 1998