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Published in: Medicine, Health Care and Philosophy 4/2020

Open Access 01-12-2020 | Scientific Contribution

«If you give them your little finger, they’ll tear off your entire arm»: losing trust in biobank research

Authors: Lars Ursin, Borgunn Ytterhus, Erik Christensen, John-Arne Skolbekken

Published in: Medicine, Health Care and Philosophy | Issue 4/2020

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Abstract

Why do some people withdraw from biobank studies? To our knowledge, very few studies have been done on the reflections of biobank ex-participants. In this article, we report from such a study. 16 years ago, we did focus group interviews with biobank participants and ex-participants. We found that the two groups interestingly shared worries concerning the risks involved in possible novel uses of their biobank material, even though they drew opposite conclusions from their worries. Revisiting these interviews today reveals a remarkable relevance to present concerns, since the possible developments that worried ex-participants and participants 16 years ago now are becoming realities. Drawing on conceptual distinctions by sociologist and philosopher Niklas Luhmann, we argue that while ex-participants express a loss of trust in the biobank institution to manage the use of their biobank material in a legitimate way, remaining participants expressed confidence in the management of the biobank institution to secure their interests. This analysis brings out important aspects of emerging trends in biobank research participation.
Literature
go back to reference Aramoana, Jaclyn, and Jonathan Koea. 2020. An integrative review of barriers to indigenous peoples’ participation in biobanking and genomic research. JCO Global Oncology 6: 83–91.CrossRef Aramoana, Jaclyn, and Jonathan Koea. 2020. An integrative review of barriers to indigenous peoples’ participation in biobanking and genomic research. JCO Global Oncology 6: 83–91.CrossRef
go back to reference Boers, Sarah N., Johannes J.M. van Delden, and Annelien L. Bredenoord. 2015. Broad consent is consent for governance. American Journal of Bioethics 15 (9): 53–55.CrossRef Boers, Sarah N., Johannes J.M. van Delden, and Annelien L. Bredenoord. 2015. Broad consent is consent for governance. American Journal of Bioethics 15 (9): 53–55.CrossRef
go back to reference Flavio, D’Abramo, Jan Schildmann, and Jochen Vollmann. 2015. Research participants’ perceptions and views on consent for biobank research: A review of empirical data and ethical analysis. BMC Medical Ethics 16: 60.CrossRef Flavio, D’Abramo, Jan Schildmann, and Jochen Vollmann. 2015. Research participants’ perceptions and views on consent for biobank research: A review of empirical data and ethical analysis. BMC Medical Ethics 16: 60.CrossRef
go back to reference De Vries, RG, G. Raymond, Kerry A. Ryan, Linda Gordon, Chris D. Krenz, Tom Tomlinson, Scott Jewell, and Scott Y.H. Kim. 2019. Biobanks and the moral concerns of donors: A democratic deliberation. Qualitative Health Research 29 (13): 1942–1953.CrossRef De Vries, RG, G. Raymond, Kerry A. Ryan, Linda Gordon, Chris D. Krenz, Tom Tomlinson, Scott Jewell, and Scott Y.H. Kim. 2019. Biobanks and the moral concerns of donors: A democratic deliberation. Qualitative Health Research 29 (13): 1942–1953.CrossRef
go back to reference Domaradzki, Jan, and Jakub Pawlikowski. 2019. Public attitudes toward biobanking of human biological material for research purposes: A literature review. International Journal of Environmental Research and Public Health 16 (12): 2209.CrossRef Domaradzki, Jan, and Jakub Pawlikowski. 2019. Public attitudes toward biobanking of human biological material for research purposes: A literature review. International Journal of Environmental Research and Public Health 16 (12): 2209.CrossRef
go back to reference Garrison, Nanibaa’ A, Nila A. Sathe, Armand H. Matheny Antommaria, Ingrid A. Holm, Saskia C. Sanderson, Maureen E. Smith, Melissa L. McPheeters, and Ellen W. Clayton., 2016. A systematic literature review of individuals’ perspectives on broad consent and data sharing in the United States. Genetics in Medicine 18 (7): 663–671.CrossRef Garrison, Nanibaa’ A, Nila A. Sathe, Armand H. Matheny Antommaria, Ingrid A. Holm, Saskia C. Sanderson, Maureen E. Smith, Melissa L. McPheeters, and Ellen W. Clayton., 2016. A systematic literature review of individuals’ perspectives on broad consent and data sharing in the United States. Genetics in Medicine 18 (7): 663–671.CrossRef
go back to reference Goisauf, Melania, and Anna P. Durnová. 2019. From engaging publics to engaging knowledges: Enacting “appropriateness” in the Austrian biobank infrastructure. Public Understanding of Science 28 (3): 275–289.CrossRef Goisauf, Melania, and Anna P. Durnová. 2019. From engaging publics to engaging knowledges: Enacting “appropriateness” in the Austrian biobank infrastructure. Public Understanding of Science 28 (3): 275–289.CrossRef
go back to reference Grimen, Harald. 2009. Hva er tillit? [What is trust?]. Oslo: Universitetsforlaget. Grimen, Harald. 2009. Hva er tillit? [What is trust?]. Oslo: Universitetsforlaget.
go back to reference Hardin, Russell. 2002. Trust and trustworthiness. New York: Russell Sage Foundation. Hardin, Russell. 2002. Trust and trustworthiness. New York: Russell Sage Foundation.
go back to reference Helgesson, Gert, Mats G. Hansson, Johnny Ludvigsson, and Ulrica Swartling. 2009. Practical matters, rather than lack of trust, motivate nono-participation in a long-term cohort trial. Pediatric Diabetes 10: 408–412.CrossRef Helgesson, Gert, Mats G. Hansson, Johnny Ludvigsson, and Ulrica Swartling. 2009. Practical matters, rather than lack of trust, motivate nono-participation in a long-term cohort trial. Pediatric Diabetes 10: 408–412.CrossRef
go back to reference Jostein, Holmen, May Britt Kjelsaas, Øystein Krüger, Hanne Ellekjær, Grete Bratberg, Turid LingaasHolmen, Kristian Midthjell, Per ArneStavnås, and Steinar Krogstad. 2004. Befolkningens holdninger til genetisk epidemiologi illustrert ved spørsmål om fornyet samtykke til 61.246 personer—Helseundersøkelsen i Nord-Trøndelag (HUNT). Norsk Epidemiologi 14: 27–31. Jostein, Holmen, May Britt Kjelsaas, Øystein Krüger, Hanne Ellekjær, Grete Bratberg, Turid LingaasHolmen, Kristian Midthjell, Per ArneStavnås, and Steinar Krogstad. 2004. Befolkningens holdninger til genetisk epidemiologi illustrert ved spørsmål om fornyet samtykke til 61.246 personer—Helseundersøkelsen i Nord-Trøndelag (HUNT). Norsk Epidemiologi 14: 27–31.
go back to reference Holmström, Susanne. 2005. Reframing public relations: The evolution of a reflective paradigm for organizational legitimization. Public Relations Review 31 (4): 497–504.CrossRef Holmström, Susanne. 2005. Reframing public relations: The evolution of a reflective paradigm for organizational legitimization. Public Relations Review 31 (4): 497–504.CrossRef
go back to reference Holmström, Susanne. 2007. Niklas Luhmann: contingency, Risk, trust and reflection. Public Relations Review 33 (3): 255–262.CrossRef Holmström, Susanne. 2007. Niklas Luhmann: contingency, Risk, trust and reflection. Public Relations Review 33 (3): 255–262.CrossRef
go back to reference Alma, Husedzinovic, Dominik Ose, Christoph Schickhardt, Stefan Fröhling, and Eva C. Winkler. 2015. Stakeholders’ perspectives on biobank-based genomic research: Systematic review of the literature. European Journal of Human Genetics 23: 1607–1614.CrossRef Alma, Husedzinovic, Dominik Ose, Christoph Schickhardt, Stefan Fröhling, and Eva C. Winkler. 2015. Stakeholders’ perspectives on biobank-based genomic research: Systematic review of the literature. European Journal of Human Genetics 23: 1607–1614.CrossRef
go back to reference Kowal, Emma, Ashley Greenwood, and Rebekah E. McWirther. 2015. All in the blood: A review of aboriginal Australians’ cultural beliefs about blood and implications for biospecimen research. Journal of Empirical Research on Human Research Ethics 10 (4): 347–359.CrossRef Kowal, Emma, Ashley Greenwood, and Rebekah E. McWirther. 2015. All in the blood: A review of aboriginal Australians’ cultural beliefs about blood and implications for biospecimen research. Journal of Empirical Research on Human Research Ethics 10 (4): 347–359.CrossRef
go back to reference Kraft, Stephanie A., Mildred K. Cho, Katherine Gillespie, Meghan Halley, Nina Varsava, Kelly E. Ormond, Harold S. Luft, Benjamin S. Wilfond, and Sandra Soo-Jin Lee. 2018. Beyond consent: Building trusting relationships with diverse populations in precision medicine research. American Journal of Bioethics 18 (4): 3–20.CrossRef Kraft, Stephanie A., Mildred K. Cho, Katherine Gillespie, Meghan Halley, Nina Varsava, Kelly E. Ormond, Harold S. Luft, Benjamin S. Wilfond, and Sandra Soo-Jin Lee. 2018. Beyond consent: Building trusting relationships with diverse populations in precision medicine research. American Journal of Bioethics 18 (4): 3–20.CrossRef
go back to reference Kvale, S. 1996. Interviews: An introduction to qualitative research interviewing. Thousand Oaks, CA: Sage Publications. Kvale, S. 1996. Interviews: An introduction to qualitative research interviewing. Thousand Oaks, CA: Sage Publications.
go back to reference Lee, Sandrea S.-J., Mildred K. Cho, Stephanie A. Kraft, Nina Varsava, Katie Gillespie, Kelly E. Ormond, Benjamin S. Wilfond, and David Magnus. 2019. “I don’t want to be Henrietta Lacks”: Diverse patient perspectives on donating biospecimens for precision medicine research. Genetics in Medicine 21 (1): 107–113.CrossRef Lee, Sandrea S.-J., Mildred K. Cho, Stephanie A. Kraft, Nina Varsava, Katie Gillespie, Kelly E. Ormond, Benjamin S. Wilfond, and David Magnus. 2019. “I don’t want to be Henrietta Lacks”: Diverse patient perspectives on donating biospecimens for precision medicine research. Genetics in Medicine 21 (1): 107–113.CrossRef
go back to reference Luhmann, Niklas. 1979. Trust and power. New York: Wiley. Luhmann, Niklas. 1979. Trust and power. New York: Wiley.
go back to reference Luhmann, Niklas. 1990. Soziologische Aufklärung. Opladen: Westdeutscher Verlag.CrossRef Luhmann, Niklas. 1990. Soziologische Aufklärung. Opladen: Westdeutscher Verlag.CrossRef
go back to reference Luhmann, Niklas. 2000/1988. Familiarity, confidence, trust: Problems and alternatives. In Trust: Making and breaking cooperative relations, ed. Diego Gambetta, 94–107. Oxford: Basil Blackwell. Luhmann, Niklas. 2000/1988. Familiarity, confidence, trust: Problems and alternatives. In Trust: Making and breaking cooperative relations, ed. Diego Gambetta, 94–107. Oxford: Basil Blackwell.
go back to reference Melas, Philippe A., Louise K. Sjöholm, Tord Forsner, Maigun Edhborg, Niklas Juth, Yvonne Forsell, and Catharina Lavebratt. 2010. Examining the public refusal to consent to DNA biobanking: Empirical data from a Swedish population-based study. Journal of Medical Ethics 36: 93–98.CrossRef Melas, Philippe A., Louise K. Sjöholm, Tord Forsner, Maigun Edhborg, Niklas Juth, Yvonne Forsell, and Catharina Lavebratt. 2010. Examining the public refusal to consent to DNA biobanking: Empirical data from a Swedish population-based study. Journal of Medical Ethics 36: 93–98.CrossRef
go back to reference Nooruddin, Mohammed, Courtney Scherr, Paula Friedman, Ramesh Subrahmanyam, Jeff Banagan, Diana Moreno, Myurani Sathyanarayanan, Edith Nutescu, Tharani Jeyaram, Mary Harris, Honghong Zhang, Adriana Rodriguez, Mohammed Shaazuddin, Minoli Perera, and Matthew Tuck. 2020. Why African Americans say “No”: A study of pharmacogenomic research participation. Ethnicity & Disease 30 (Suppl 1): 159–166.CrossRef Nooruddin, Mohammed, Courtney Scherr, Paula Friedman, Ramesh Subrahmanyam, Jeff Banagan, Diana Moreno, Myurani Sathyanarayanan, Edith Nutescu, Tharani Jeyaram, Mary Harris, Honghong Zhang, Adriana Rodriguez, Mohammed Shaazuddin, Minoli Perera, and Matthew Tuck. 2020. Why African Americans say “No”: A study of pharmacogenomic research participation. Ethnicity & Disease 30 (Suppl 1): 159–166.CrossRef
go back to reference Offe, Claus. 1999. How can we trust our fellow citizens? In Democracy and trust, ed. Mark E. Warren, 42–87. Cambridge: Cambridge University Press.CrossRef Offe, Claus. 1999. How can we trust our fellow citizens? In Democracy and trust, ed. Mark E. Warren, 42–87. Cambridge: Cambridge University Press.CrossRef
go back to reference Ridgeway, J.L., L.C. Han, J.E. Olson, K.A. Lackore, B.A. Koenig, T.J. Beebe, and J.Y. Ziegenfuss. 2013. Potential bias in the bank: What distinguishes refusers, nonresponders and participants in a clinic-based biobank? Public Health Genomics 16: 118–126.CrossRef Ridgeway, J.L., L.C. Han, J.E. Olson, K.A. Lackore, B.A. Koenig, T.J. Beebe, and J.Y. Ziegenfuss. 2013. Potential bias in the bank: What distinguishes refusers, nonresponders and participants in a clinic-based biobank? Public Health Genomics 16: 118–126.CrossRef
go back to reference Sanderson, Saskia C., Kyle B. Brothers, Nathaniel D. Mercaldo, Ellen Wright Clayton, Armand H. MathenyAntommaria, Sharon A. Aufox, Murray H. Brilliant, Diego Campos, David S. Carrell, John J.M. Connolly, Pat Conway, Stephanie M. Fullerton, Nanibaa A. Garrison, Carol R. Horowitz, Gail P. Jarvik, David Kaufman, Terrie E. Kitchner, Rongling Li, Evette Ludman, Catherine A. McCarty, Jennifer B. McCormick, Valerie D. McManus, Melanie F. Myers, Aaron Scrol, Janet L. Williams, Martha J. Shrubsole, Jonathan S. Schildcrout, Maureen E. Smith, and Ingrid A. Holm. 2017. Public attitudes toward consent and data sharing in biobank research: A large multi-site experimental survey in the US. American Journal of Human Genetics 100: 414–427.CrossRef Sanderson, Saskia C., Kyle B. Brothers, Nathaniel D. Mercaldo, Ellen Wright Clayton, Armand H. MathenyAntommaria, Sharon A. Aufox, Murray H. Brilliant, Diego Campos, David S. Carrell, John J.M. Connolly, Pat Conway, Stephanie M. Fullerton, Nanibaa A. Garrison, Carol R. Horowitz, Gail P. Jarvik, David Kaufman, Terrie E. Kitchner, Rongling Li, Evette Ludman, Catherine A. McCarty, Jennifer B. McCormick, Valerie D. McManus, Melanie F. Myers, Aaron Scrol, Janet L. Williams, Martha J. Shrubsole, Jonathan S. Schildcrout, Maureen E. Smith, and Ingrid A. Holm. 2017. Public attitudes toward consent and data sharing in biobank research: A large multi-site experimental survey in the US. American Journal of Human Genetics 100: 414–427.CrossRef
go back to reference Seligman, Adam B. 1998. Trust and sociability: On the limits of confidence and role expectations. American Journal of Economics and Sociology 57 (4): 391–404.CrossRef Seligman, Adam B. 1998. Trust and sociability: On the limits of confidence and role expectations. American Journal of Economics and Sociology 57 (4): 391–404.CrossRef
go back to reference Skolbekken, J.A., L.Ø. Ursin, B. Solberg, E. Christensen, and B. Ytterhus. 2005. Not worth the paper it's written on? Informed consent and biobank research in a Norwegian context. Critical Public Health 15 (4): 335–347.CrossRef Skolbekken, J.A., L.Ø. Ursin, B. Solberg, E. Christensen, and B. Ytterhus. 2005. Not worth the paper it's written on? Informed consent and biobank research in a Norwegian context. Critical Public Health 15 (4): 335–347.CrossRef
go back to reference Steinsbekk, Kristin Solum, and B. Berge Solberg. 2011. Biobanks-when is re-consent necessary? Public Health Ethics 4 (3): 236–250.CrossRef Steinsbekk, Kristin Solum, and B. Berge Solberg. 2011. Biobanks-when is re-consent necessary? Public Health Ethics 4 (3): 236–250.CrossRef
go back to reference Williams, Pamela Holtzclaw, Lynne S. Nemeth, Jennifer E. Sanner, and Lorraine Q. Frazier. 2013. Thematic analysis of cardiac care patients’ explanations for declining contribution to a genomic research-based biobank. American Journal of Critical Care 22 (4): 320–327.CrossRef Williams, Pamela Holtzclaw, Lynne S. Nemeth, Jennifer E. Sanner, and Lorraine Q. Frazier. 2013. Thematic analysis of cardiac care patients’ explanations for declining contribution to a genomic research-based biobank. American Journal of Critical Care 22 (4): 320–327.CrossRef
Metadata
Title
«If you give them your little finger, they’ll tear off your entire arm»: losing trust in biobank research
Authors
Lars Ursin
Borgunn Ytterhus
Erik Christensen
John-Arne Skolbekken
Publication date
01-12-2020
Publisher
Springer Netherlands
Published in
Medicine, Health Care and Philosophy / Issue 4/2020
Print ISSN: 1386-7423
Electronic ISSN: 1572-8633
DOI
https://doi.org/10.1007/s11019-020-09969-w

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