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The Ethics and Governance of Human Genetic Databases

The Ethics and Governance of Human Genetic Databases European Perspectives

Author: Matti Hayry; Ruth Chadwick; Vilhjalmur Arnasun; Gardar Arnason
Publisher: Cambridge University Press
ISBN: 9780521856621
Published In: April 2007
Format: Hardback
Jurisdiction: European Union ? Disclaimer:
Countri(es) stated herein are used as reference only

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Contents

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The Medical Biobank of Umea in Sweden, deCODE's Health Sector Database in Iceland, the Estonian Genome Project and the UK Biobank contain health data and genetic data from large populations. Some include genealogical or lifestyle information. They are resources for research in human genetics and medicine, exploring interaction between genes, lifestyle, environmental factors and health and diseases.
The collection, storage and use of this data raise ethical, legal and social issues. In this book, bioethics scholars examine whether existing ethical frameworks and social policies reflect people's concerns, and how they may need to change in light of new scientific and technological developments. The ethical issues of social justice, genetic discrimination, informational privacy, trust in science and consent to participation in database research are analyzed, whilst an empirical survey, conducted in the four countries, demonstrates public views of privacy and related moral values in the context of human genetic databases.
- Provides the reader with new information and analysis
- Involves a range of disciplines and national perspectives
- Deals with cutting edge issues affecting the future of health care
Contents:
Introduction Vilhjalmur Arnason
Part I. Background:
1. On human genetic databases Gardar Arnason
2. American principles, European values, and the mezzanine rules of ethical genetic data banking Matti Hayry and Tuija Takala
3. Languages of privacy Salvor Nordal
Part II. Social Concerns:
4. A sociological perspective: public perceptions of privacy and their trust in institutions managing and regulating genetic databases Kjell E. Eriksson, Margret L. Gudmundsdottir, Kulliki Korts, Sue Weldon
5. Estonia Kulliki Korts
6. Iceland Margret Lilja Gudmundsdottir and Salvor Nordal
7. Sweden Kjell E. Eriksson
8. United Kingdom Sue Weldon
9. Public discourses on human genetic databases Piia Tammpuu
Part III. Legal Issues:
10. Regulating human genetic databases in Europe Jane Kaye
11. Consent and population genetic databases Hordur Helgi Helgason
12. Third party's interests in population genetic databases Lotta Wendel
13. Transforming principles of biolaw into national legislation Ants Nomper
14. Governance of population genetic databases Susan M. C. Gibbons
15. The legal jigsaw governing population genetic databases Jane Kaye
Part IV. Ethical Questions:
16. Introduction Vilhjalmur Arnason
17. Pursuing equality: questions of Social justice and population genomics Sarah Wilson and Ruth Chadwick
18. Benefit-sharing and biobanks Kadri Simm
19. Genetic discrimination Lena Halldenius
20. Privacy Salvor Nordal
21. Trust Margit Sutrop
22. Consent Sigurdur Kristinsson and Vilhjalmur Arnason
Part V. Political Considerations:
23. Impact of biobanks on ethical frameworks Ruth Chadwick and Mark Cutter
24. Genetics, rhetoric and policy Gardar Arnason
25. Genetic databases and governance Rainer Kattel
26. Conclusion: bioethical analysis of the results Matti Hayry and Tuija Takala.