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Published in: Medicine, Health Care and Philosophy 1/2019

01-03-2019 | Scientific Contribution

“I would rather have it done by a doctor”—laypeople’s perceptions of direct-to-consumer genetic testing (DTC GT) and its ethical implications

Authors: Manuel Schaper, Sabine Wöhlke, Silke Schicktanz

Published in: Medicine, Health Care and Philosophy | Issue 1/2019

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Abstract

Direct-to-consumer genetic testing (DTC GT) has been available for several years now, with varying degrees of regulation across different countries. Despite a restrictive legal framework it is possible for consumers to order genetic tests from companies located in other countries. However, German laypeople’s awareness and perceptions of DTC GT services is still unexplored. We conducted seven focus groups (participants n = 43) with German laypeople to explore their perceptions of and attitudes towards commercial genetic testing and its ethical implications. Participants were critical towards DTC GT. Criticism was directed at health-related, predictive testing, while lifestyle tests were accepted and even welcomed to some extent. Participants expressed strong reservations regarding commercial provision of genetic diagnostics and expressed a lack of trust in respective companies. They preferred non-commercial distribution within the public healthcare system. Participants also expressed high expectations of physicians’ abilities to interpret information obtained via DTC GT companies and provide counseling. Legal restrictions on commercial distribution of genetic tests were opposed, with participants arguing that it should be available to consumers. DTC GT companies are not perceived as trustworthy when compared to the public healthcare system and its professional ethical standards and practices. Laypeople rated general consumer autonomy higher than their own concerns, thus recommending against strong legal regulation. We conclude that medicine’s trustworthiness may be negatively affected if commercial provision is not visibly opposed by the medical professions, while DTC GT companies may gain in trustworthiness if they adapt to standards and practices upheld in medicine.
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Footnotes
1
Conducting a web search in early 2017, we found about 90 companies worldwide marketing genetic/genomic tests or interpretation of test results. A recent study by Plöthner et al. (2017) identified a total of 35 companies worldwide offering health-related testing, which is theoretically available for German residents.
 
2
Personal experience means that the person has undergone genetic or genomic testing in the past or witnessed it in a relative or another person. Experience with prenatal diagnostics was not considered as personal experience with genetic testing in this sense, which is why other participants were preferred during recruitment.
 
3
Lifestyle tests in this context means genetic tests delivering information on how to improve diet and exercise as well as tests serving a purely recreational or entertainment purpose.
 
4
Examples: coronary heart disease—50.2% risk/average risk 46.8%; obesity—63.4% risk/average risk 63.9%.
 
Literature
go back to reference Anderson, Emily E., and Katherine Wasson. 2015. Personal narratives of genetic testing: Expectations, emotions, and impact on self and family. Narrative Inquiry in Bioethics 5 (3): 229–235.CrossRef Anderson, Emily E., and Katherine Wasson. 2015. Personal narratives of genetic testing: Expectations, emotions, and impact on self and family. Narrative Inquiry in Bioethics 5 (3): 229–235.CrossRef
go back to reference Berg, Bruce L. 2007. Qualitative research methods for the social sciences. Boston: Pearson/Allyn & Bacon. Berg, Bruce L. 2007. Qualitative research methods for the social sciences. Boston: Pearson/Allyn & Bacon.
go back to reference Bollinger, Juli Murphy, Robert C. Green, and David Kaufman. 2013. Attitudes about regulation among direct-to-consumer genetic testing customers. Genetic Testing and Molecular Biomarkers 17 (5): 424–428.CrossRef Bollinger, Juli Murphy, Robert C. Green, and David Kaufman. 2013. Attitudes about regulation among direct-to-consumer genetic testing customers. Genetic Testing and Molecular Biomarkers 17 (5): 424–428.CrossRef
go back to reference Critchley, Christine, Dianne Nicol, Margaret Otlowski, and Don Chalmers. 2015. Public reaction to direct-to-consumer online genetic tests: Comparing attitudes, trust and intentions across commercial and conventional providers. Public Understanding of Science 24 (6): 731–750.CrossRef Critchley, Christine, Dianne Nicol, Margaret Otlowski, and Don Chalmers. 2015. Public reaction to direct-to-consumer online genetic tests: Comparing attitudes, trust and intentions across commercial and conventional providers. Public Understanding of Science 24 (6): 731–750.CrossRef
go back to reference Gollust, Sarah E., Erynn S. Gordon, C. Zayac, Georgia Griffin, M. F. Christman, R. E. Pyeritz, Lisa Wawak, and Barbara A. Bernhardt. 2012. Motivations and perceptions of early adopters of personalized genomics: Perspectives from research participants. Public Health Genomics 15 (1): 22–30. https://doi.org/10.1159/000327296.CrossRef Gollust, Sarah E., Erynn S. Gordon, C. Zayac, Georgia Griffin, M. F. Christman, R. E. Pyeritz, Lisa Wawak, and Barbara A. Bernhardt. 2012. Motivations and perceptions of early adopters of personalized genomics: Perspectives from research participants. Public Health Genomics 15 (1): 22–30. https://​doi.​org/​10.​1159/​000327296.CrossRef
go back to reference Gordon, Erynn S., Georgia Griffin, Lisa Wawak, Hauchie Pang, E. Sarah, Gollust, and Barbara A. Bernhardt. 2012. It’s not like judgment day”: Public understanding of and reactions to personalized genomic risk information. Journal of Genetic Counseling 21 (3): 423–432. https://doi.org/10.1007/s10897-011-9476-4.CrossRef Gordon, Erynn S., Georgia Griffin, Lisa Wawak, Hauchie Pang, E. Sarah, Gollust, and Barbara A. Bernhardt. 2012. It’s not like judgment day”: Public understanding of and reactions to personalized genomic risk information. Journal of Genetic Counseling 21 (3): 423–432. https://​doi.​org/​10.​1007/​s10897-011-9476-4.CrossRef
go back to reference Karsch, Fabian. 2015. Medizin zwischen Markt und Moral. Zur Kommerzialisierung ärztlicher Handlungsfelder. Bielefeld: Transcript. Karsch, Fabian. 2015. Medizin zwischen Markt und Moral. Zur Kommerzialisierung ärztlicher Handlungsfelder. Bielefeld: Transcript.
go back to reference Krippendorf, Klaus. 2013. Content analysis. An introduction to its methodology. Los Angeles: Sage. Krippendorf, Klaus. 2013. Content analysis. An introduction to its methodology. Los Angeles: Sage.
go back to reference Metschke, Rainer, and Rita Wellbrock. 2002. Datenschutz in Wissenschaft und Forschung. Materialien zum Datenschutz 28. Metschke, Rainer, and Rita Wellbrock. 2002. Datenschutz in Wissenschaft und Forschung. Materialien zum Datenschutz 28.
go back to reference O’Doherty, Kieran C., Emily Christofides, Jeffery Yen, Heidi Beate Bentzen, Wylie Burke, Nina Hallowell, Barbara A. Koenig, and Donald J. Willison. 2016. If you build it, they will come: Unintended future uses of organised health data collections. BMC Medical Ethics 17 (1): 54. https://doi.org/10.1186/s12910-016-0137-x.CrossRef O’Doherty, Kieran C., Emily Christofides, Jeffery Yen, Heidi Beate Bentzen, Wylie Burke, Nina Hallowell, Barbara A. Koenig, and Donald J. Willison. 2016. If you build it, they will come: Unintended future uses of organised health data collections. BMC Medical Ethics 17 (1): 54. https://​doi.​org/​10.​1186/​s12910-016-0137-x.CrossRef
go back to reference O’Neill, Onora. 2002. Autonomy and trust in bioethics. Cambridge: Cambridge University Press.CrossRef O’Neill, Onora. 2002. Autonomy and trust in bioethics. Cambridge: Cambridge University Press.CrossRef
go back to reference Obar, Jonathan A., and Anne Oeldorf-Hirsch. 2016. The biggest lie on the internet: Ignoring the privacy policies and terms of service policies of social networking services. Paper presented at the TPRC 44: The 44th research conference on communication, information and internet policy 2016. https://doi.org/10.2139/ssrn.2757465. Obar, Jonathan A., and Anne Oeldorf-Hirsch. 2016. The biggest lie on the internet: Ignoring the privacy policies and terms of service policies of social networking services. Paper presented at the TPRC 44: The 44th research conference on communication, information and internet policy 2016. https://​doi.​org/​10.​2139/​ssrn.​2757465.
go back to reference Oliveri, Serana, Marianna Masiero, Paola Arnaboldi, Ilaria Cutica, Chiara Fioretti, and Gabriella Pravettoni. 2016. Health orientation, knowledge, and attitudes toward genetic testing and personalized genomic services: Preliminary data from an Italian sample. BioMed Research International 2016: 6824581. https://doi.org/10.1155/2016/6824581.CrossRef Oliveri, Serana, Marianna Masiero, Paola Arnaboldi, Ilaria Cutica, Chiara Fioretti, and Gabriella Pravettoni. 2016. Health orientation, knowledge, and attitudes toward genetic testing and personalized genomic services: Preliminary data from an Italian sample. BioMed Research International 2016: 6824581. https://​doi.​org/​10.​1155/​2016/​6824581.CrossRef
go back to reference Plöthner, Marika, Mike Klora, Daniel Rudolph, and Johann-Matthias Graf von der Schulenburg. 2017. Health-related genetic direct-to-consumer tests in the German setting: The available offer and the potential implications for a solidarily financed health-care system. Public Health Genomics. https://doi.org/10.1159/000477559.CrossRef Plöthner, Marika, Mike Klora, Daniel Rudolph, and Johann-Matthias Graf von der Schulenburg. 2017. Health-related genetic direct-to-consumer tests in the German setting: The available offer and the potential implications for a solidarily financed health-care system. Public Health Genomics. https://​doi.​org/​10.​1159/​000477559.CrossRef
go back to reference Roberts, J. Scott, Michele C. Gornick, Deanna Alexis Carere, Wendy R. Uhlmann, Mack T. Ruffin, and Robert C. Green. 2017. Direct-to-consumer genetic testing: User motivations, decision making, and perceived utility of results. Public Health Genomics. https://doi.org/10.1159/000455006.CrossRef Roberts, J. Scott, Michele C. Gornick, Deanna Alexis Carere, Wendy R. Uhlmann, Mack T. Ruffin, and Robert C. Green. 2017. Direct-to-consumer genetic testing: User motivations, decision making, and perceived utility of results. Public Health Genomics. https://​doi.​org/​10.​1159/​000455006.CrossRef
go back to reference Salm, Melissa, Kristopher Abbate, Paul Appelbaum, Ruth Ottman, Wendy Chung, Karen Marder, Cheng-Shiun Leu, Roy Alcalay, Jill Goldmann, Alexander Malik Curtis, Christopher Leech, Katherine Johansen Taber, and Robert Klitzmann. 2014. Use of genetic tests among neurologists and psychiatrists: Knowledge, attitudes, behaviors, and needs for training. Journal of Genetic Counseling 23 (2): 156–163. https://doi.org/10.1007/s10897-013-9624-0.CrossRef Salm, Melissa, Kristopher Abbate, Paul Appelbaum, Ruth Ottman, Wendy Chung, Karen Marder, Cheng-Shiun Leu, Roy Alcalay, Jill Goldmann, Alexander Malik Curtis, Christopher Leech, Katherine Johansen Taber, and Robert Klitzmann. 2014. Use of genetic tests among neurologists and psychiatrists: Knowledge, attitudes, behaviors, and needs for training. Journal of Genetic Counseling 23 (2): 156–163. https://​doi.​org/​10.​1007/​s10897-013-9624-0.CrossRef
go back to reference Sherman, Kerry, Laura-Kate Shaw, Katrina Champion, Fernanda Caldeira, and Margaret McCaskill. 2015. The effect of disease risk probability and disease type on interest in clinic-based versus direct-to-consumer genetic testing services. Journal of Behavioral Medicine 38 (5): 706–714.CrossRef Sherman, Kerry, Laura-Kate Shaw, Katrina Champion, Fernanda Caldeira, and Margaret McCaskill. 2015. The effect of disease risk probability and disease type on interest in clinic-based versus direct-to-consumer genetic testing services. Journal of Behavioral Medicine 38 (5): 706–714.CrossRef
go back to reference Su, Pascal. 2013. Direct-to-consumer genetic testing: A comprehensive view. The Yale Journal of Biology and Medicine 86 (3): 359–365. Su, Pascal. 2013. Direct-to-consumer genetic testing: A comprehensive view. The Yale Journal of Biology and Medicine 86 (3): 359–365.
Metadata
Title
“I would rather have it done by a doctor”—laypeople’s perceptions of direct-to-consumer genetic testing (DTC GT) and its ethical implications
Authors
Manuel Schaper
Sabine Wöhlke
Silke Schicktanz
Publication date
01-03-2019
Publisher
Springer Netherlands
Published in
Medicine, Health Care and Philosophy / Issue 1/2019
Print ISSN: 1386-7423
Electronic ISSN: 1572-8633
DOI
https://doi.org/10.1007/s11019-018-9837-y

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