Skip to main content

Biotechnology, Genetic Information, and Community

From Individual Rights to Social Duties?

  • Chapter
Genetic Information

Abstract

One of the main ethical problems in biomedical issues has been deciding who should have access to our genetic information and why. In this article I set this issue along with other ethical problems of biomedicine within a framework based on the contemporary liberal-communitarian debate, and discuss whether individual rights or social duties should have priority in the use of genetic or other health related information. However, instead of attempting to provide a clear normative stand, I want to discuss this issue from the point of view of analytical political philosophy. This means that my purpose is to clarify the complex relationship between the liberal ideal of political justice, the communitarian ethical approach and individual’s moral judgement in the issues of biomedicine. My starting point is the contemporary shift of emphasis from the liberal concept of justice towards a more communitarian ethical approach. This can be seen in the Western world in the recent tendency to supplement and balance individual rights with considerations of individual responsibilities.1 What I see should be acknowledge here is that even if the promotion of individuals’ social duties is now evidently gaining emphasis in Western medical practice, the academic discussions as well as political and legal debates are still mainly based on the ethical demands of informed consent, individual autonomy and individual rights. This may lead us to a curious situation in which explicitly individualistic and liberal philosophical, political and legal discourse still uses the language of rights,2 while in practice there is, at least implicitly, increasing social pressure for individuals to accept their social duties and give ‘the common good’ priority over their personal moral judgement.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Annas, G., Glantz, L, and Roche, P. (1995) The Genetic Privacy Act and Commentary at url http://www.ornl.gov/TechResources/...ome/resource/privacy/privacyI-5.html.

  • Avineri, S. & de-Shalit, A. (1992), Communitarianism and Individualism. Oxford University Press, New York.

    Google Scholar 

  • Chadwick, R. (1997), ‘The Philosophy of the right to know and the right not to know’ in Chadwick, Ruth, Levitt, Mairi and Shickle, Darren (eds.), The Right to Know and the Right not to Know, Avebury: Aldershot, Brookfield USA, Hong Kong, Singapore, Sydney.

    Google Scholar 

  • Chadwick, R., Levitt, M., and Shickle, D. (1997), ‘Introduction’ (1997) in Chadwick, R., Levitt, M., and Shickle, D. The Right to Know and the Right not to Know. Avebury: Aldershot, Brookfield USA, Hong Kong, Singapore, Sydney.

    Google Scholar 

  • Childress, J. & Beauchamp, T. (1979), Principles of Biomedical Ethics 4th ed. Oxford University Press: New York.

    Google Scholar 

  • Danish Council of Ethics (1993), Ethics and Mapping of the Human Genome, Protection of Sensitive Personal Information, The Danish Council of Ethics: Copenhagen.

    Google Scholar 

  • Declaration of Helsinki (1964), Recommendations guiding physicians in biomedical research involving human subjects, the 18th World medical Assembly, Bulletin of Medical Ethics, No. 128, May 1997, Bioethics Publications Ltd, Royal Society of Medicine Press: London.

    Google Scholar 

  • Etzioni, A.(1996), The Spirit of Community: The Reinvention of American Society. Touchstone: New York.

    Google Scholar 

  • Etzioni, A. (1991), HIV Testing for Infants and Pregnant Women: A Case Study in Privacy and Public Health, The Communitarian Network: Washington, DC.

    Google Scholar 

  • Etzioni, A., Cassel, C, Dougherty, C, McCollister Evarts, C, Griffith, J., Nelson, J., Osterweis, M., and Wikler, D. (1997), A Communitarian Position Paper: Core Values in Health-Care Reform, A Communitarian Approach, The Communitarian Network: Washington, DC.

    Google Scholar 

  • Ezekiel, E. (1991), The Ends of Human Life: Medical Ethics in a Liberal Policy. Harvard University Press: Cambridge.

    Google Scholar 

  • Hadjiminas G. M. (1994), Ethics and human genetics, proceedings 2nd Symposium of the Council of Europe on Bioethics, Strasbourg, 30-November–2 December 1993, Publishing & Documentation Service, Council of Europe, Council of Europe Press: Strasbourg Cedex.

    Google Scholar 

  • Hare, R.M. (1993), Essays on Bioethics, Clarendon Press: Oxford.

    Google Scholar 

  • Harris, J. (1993) Wonderwoman and Superman. The Ethics of Human Biotechnology. Oxford University Press: Oxford.

    Google Scholar 

  • Hoshino, K. (ed.) (1977), Japanese and Western Bioethics: studies in moral diversity. Kluwer: Dordrecht.

    Google Scholar 

  • MacIntyre, A. (1984), After Virtue. Duckworth: London.

    Google Scholar 

  • MacIntyre, A. (1988), Whose Justice? Which Rationality? Duckworth, London.

    Google Scholar 

  • Motulsky, A. (1993), Ethics and human genetics, proceedings 2nd Symposium of the Council of Europe on Bioethics, Strasbourg, 30–November-2 December 1993, Publishing & Documentation Service, Council of Europe, Council of Europe Press: Strasbourg Cedex.

    Google Scholar 

  • Ndinya-Achola, J.O. (1995), ‘Medical Ethics, History of: Africa’ in Reich, W.T. (ed.), Encyclopedia of Bioethics (1995), revised edition vol. 2, Georgetown University, Washington. D.C. Simon & Schuster and Prentice Hall International: London, Mexico City, New Delhi, Singapore, Sidney, Toronto.

    Google Scholar 

  • Rawls, J.(I971), Theory of Justice. Harvard University Press: Cambridge.

    Google Scholar 

  • Rawls, J.(1993), Political Liberalism. Columbia University Press: New York.

    Google Scholar 

  • Royal College of Physicians (1991), Ethical Issues in Clinical Genetics, Royal College of Physicians: London.

    Google Scholar 

  • Sandel, M. (1982), Liberalism and the Limits of Justice. Cambridge University Press: Cambridge.

    Google Scholar 

  • Tangwa, G. (1996), ‘Bioethics: An African Perspective’, Bioethics Vol. 10.No 3, 183–200.

    PubMed  Google Scholar 

  • Taylor, C. (1979), Hegel and the Modern Society. Cambridge University Press: Cambridge.

    Google Scholar 

  • Taylor, C. (1989), Sources of the Self: The Making of Moral Identity. Cambridge University Press: Cambridge.

    Google Scholar 

  • The Responsive Communitarian Platform (1997), The Communitarian Network: Washington, DC, also at url http://www.edu/~ccps/RCPlatform.html.

  • Walzer, M. (1980), Radical Principles. Reflections of an Unreconstructed Democrat. Basic Books: New York.

    Google Scholar 

  • Walzer, M. (1983), Spheres of Justice. Basic Books: New York.

    Google Scholar 

  • Wiesing, U. (1997), ‘Individual rights and genetics: the historical perspective. A comment on Ruth Chadwick’s paper’ in Chadwick, R., Levitt, M. and Shickle, D. (eds.) The Right to Know and the Right not to Know, Avebury: Aldershot, Brookfield USA, Hong Kong, Singapore, Sydney.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1999 Kluwer Academic/Plenum Publishers

About this chapter

Cite this chapter

Hellsten, S.K. (1999). Biotechnology, Genetic Information, and Community. In: Thompson, A.K., Chadwick, R.F. (eds) Genetic Information. Springer, Boston, MA. https://doi.org/10.1007/978-0-585-34586-4_28

Download citation

  • DOI: https://doi.org/10.1007/978-0-585-34586-4_28

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-0-306-46052-4

  • Online ISBN: 978-0-585-34586-4

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics