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Ethical Ramifications of Genetic Analysis Using DNA Arrays

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Book cover DNA Arrays

Part of the book series: Methods in Molecular Biology™ ((MIMB,volume 170))

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Abstract

Since its earliest days, the history of human genetics has been checkered with actual, perceived, and potential abuses in the application of its scientific concepts to research or clinical endeavors. Aside from obvious cases of scientific fraud and continuing controversies over natural selection and biological determinism, a long and varied history of eugenics movements grew out of the (re)discovery of Mendel’s experiments at the beginning of the twentieth century. The term eugenics was first coined by Francis Galton in 1883 and defined as the science of improving the gene pool of the human species through selective breeding. The concept was soon extended well beyond its obvious and accepted precedent of animal husbandry to encompass social as well as physical traits, as Mendelian inheritance came to be viewed as the fundamental determinant of low intelligence, mental illness, substance abuse, physical handicaps, poverty, promiscuity, prostitution, and criminality. Eugenics thus provided a logical extension to the notion that such undesirable traits could be weeded out of the population through biological means rather than traditional social welfare policy, by enactment of restricted marriage laws, mandatory sterilization, euthanasia, or outright genocide. Of course, everyone knows that such policies reached their zenith (or nadir) in Nazi Germany, where the scope of supposedly genetic social traits to be eliminated through these means expanded to include race and ethnicity.

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References

  1. Kevles, D. J. and Hood, L. (ed.) (1992) The Code of Codes: Scientific and Social Issues in the Human Genome Project, Harvard University Press, Cambridge, MA.

    Google Scholar 

  2. Nuremberg Code. (1949) Trials of War Criminals Before the Nuremberg Military Tribunals Under Control Council Law No. 10, vol. 2, U.S. Government Printing Office, Washington, DC.

    Google Scholar 

  3. National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research. (1979) The Belmont Report: Ethical Principles and Guidelines for the Protection of Human Subjects of Research, U.S. Department of Health, Education and Welfare, Washington, DC.

    Google Scholar 

  4. United States Department of Energy. (1997) Human Genome Program Report, Part 1: Overview and Progress, U.S. Department of Energy, Germantown, MD.

    Google Scholar 

  5. Grody, W. W., Kronquist, K. E., Lee, E. U., Edmond, J., and Rome, L. H. (1993) PCR-based cystic fibrosis carrier screening in a first-year medical student biochemistry laboratory. Am. J. Hum. Genet. 53, 1352–1355.

    PubMed  CAS  Google Scholar 

  6. Giardiello, F. M., Brensinger, J. D., Petersen, G. M., Luce, M. C., Hylind, L. M., Bacon, J. A., Booker, S. V., Parker, R. D., and Hamilton, S. R. (1997) The use and interpretation of commercial APC gene testing for familial adenomatous polyposis. N. Engl. J. Med. 336, 823–827.

    Article  PubMed  CAS  Google Scholar 

  7. Grody, W. W. (1999) Cystic fibrosis: Molecular diagnosis, population screening, and public policy. Arch. Pathol. Lab. Med. 123, 1041–1046.

    PubMed  CAS  Google Scholar 

  8. Geller, G., Botkin, J. R., Green, M. J., Press, N., Biesecker, B. B., Wilfond, B., Grana, G., Daly, M. B., Schneider, K., and Kahn, M. J. E. (1997) Genetic testing for susceptibility to adult-onset cancer: The process and content of informed consent. JAMA 277, 1467–1474.

    Article  PubMed  CAS  Google Scholar 

  9. Holtzman, N. A., Murphy, P. D., Watson, M. S., and Barr, P. A. (1997) Predictive genetic testing: From basic research to clinical practice. Science 278, 602–605.

    Article  PubMed  CAS  Google Scholar 

  10. Task Force on Genetic Testing. (1998) Promoting Safe and Effective Genetic Testing in the United States, Johns Hopkins University Press, Baltimore, MD.

    Google Scholar 

  11. American Society of Clinical Oncology. (1996) Statement of the American Society of Clinical Oncology: Genetic testing for cancer susceptibility. J. Clin. Oncol. 14, 81,730–81,736.

    Google Scholar 

  12. National Committee for Clinical Laboratory Standards. (1999) Molecular Diagnostic Methods for Genetic Diseases: Approved Guidelines, National Committee for Clinical Laboratory Standards, Wayne, PA.

    Google Scholar 

  13. Shattuck-Eidens, D., Oliphant, A., McClure, M., McBride, C., Gupte, J., Rubano, T., et al. (1997) BRCA1 sequence analysis in women at high risk for susceptibility mutations: Risk factor analysis and implications for genetic testing. JAMA 278, 1242–1250.

    Article  PubMed  CAS  Google Scholar 

  14. Billings, P., Cohn, M., de Cuevas, M., Beckwith, J., Alper, J., and Natowicz, M. (1992) Discrimination as a consequence of genetic testing. Am. J. Hum. Genet. 50, 476–82.

    PubMed  CAS  Google Scholar 

  15. Hudson, K. L., Rothenberg, K. H., Andrews, L. B., Kahn, M. J. E., and Collins, F. S. (1995) Genetic discrimination and health insurance: An urgent need for reform. Science 270, 391–393.

    Article  PubMed  CAS  Google Scholar 

  16. Reilly, P. R. (1998) Rethinking risks to human subjects in genetic research. Am. J. Hum. Genet. 63, 682–685.

    Article  PubMed  CAS  Google Scholar 

  17. Botkin, J. R., McMahon, W. M., Smith, K. R., and Nash, J. E. (1998) Privacy and confidentiality in the publication of pedigrees: A survey of investigators and biomedical journals. JAMA 279, 1808–1812.

    Article  PubMed  CAS  Google Scholar 

  18. Byers, P. H. and Ashkenas, J. (1998) Pedigrees—Publish? or perish the thought? Am. J. Hum. Genet. 63, 678–681.

    Article  PubMed  CAS  Google Scholar 

  19. Struewing, J. P., Abeliovich, D., Peretz, T., Avishai, N., Kaback, M. M., Collins, F. S., and Brody, L. C. (1995) The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals. Nat. Genet. 11, 198–200.

    Article  PubMed  CAS  Google Scholar 

  20. Foster, M. W., Bersten, D., and Carter, T. H. (1998) A model agreement for genetic research in socially identifiable populations. Am. J. Hum. Genet. 63, 696–702.

    Article  PubMed  CAS  Google Scholar 

  21. Juengst, E. T. (1998) Group identity and human diversity: Keeping biology straight from culture. Am. J. Hum. Genet. 63, 673–677.

    Article  PubMed  CAS  Google Scholar 

  22. Pembrey, M. E. (1998) In the light of preimplantation genetic diagnosis: Some ethical issues in medical genetics revisited. Eur. J. Hum. Genet. 6, 4–11.

    Article  PubMed  CAS  Google Scholar 

  23. Clayton, E. W., Steinberg, K. K., Khoury, M. J., Thomson, E., Andrews, L., Kahn, M. J. E., Kopelman, L. M., and Weiss, J. O. (1995) Informed consent for genetic research on stored tissue samples. JAMA 274, 1786–1792.

    Article  PubMed  CAS  Google Scholar 

  24. Knoppers, B. M. and Laberge, C. M. (1995) Research and stored tissues: Persons as sources, samples as persons? JAMA 274, 1806–1807.

    Article  PubMed  CAS  Google Scholar 

  25. Grody, W. W. (1995) Molecular pathology, informed consent, and the paraffin block. Diagn. Molec. Pathol. 4, 155–157.

    Article  CAS  Google Scholar 

  26. Grizzle, W., Grody, W. W., Noll, W. W., Sobel, M. E., Stass, S. A., Trainer, T., Travers, H., Weedn, V., and Woodruff, K. (1999) Recommended policies for uses of human tissue in research, education, and quality control. Arch. Pathol. Lab. Med. 123, 296–300.

    PubMed  CAS  Google Scholar 

  27. American Society of Human Genetics. (1996) ASHG Report: Statement on informed consent for genetic research. Am. J. Hum. Genet. 59, 471–474.

    Google Scholar 

  28. Merz, J. F., Sankar, P., Taube, S. E., and LiVolsi, V. (1997) Use of human tissues in research: Clarifying clinician and researcher roles and information flows. J. Invest. Med. 45, 252–257.

    CAS  Google Scholar 

  29. Grody, W. W. and Watson, M. S. (1997) Those elusive molecular diagnostics CPT codes. Diagn. Mol. Pathol. 6, 131–133.

    Article  PubMed  CAS  Google Scholar 

  30. Garrett, C. T. and Ferreira-Gonzalez, A. (1996) FDA regulation of analyte-specific reagents (ASRs): Implications for nucleic acid-based molecular testing. Diagn. Mol. Pathol. 5, 151–153.

    Article  PubMed  CAS  Google Scholar 

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© 2001 Humana Press Inc.

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Grody, W.W. (2001). Ethical Ramifications of Genetic Analysis Using DNA Arrays. In: Rampal, J.B. (eds) DNA Arrays. Methods in Molecular Biology™, vol 170. Humana Press. https://doi.org/10.1385/1-59259-234-1:53

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  • DOI: https://doi.org/10.1385/1-59259-234-1:53

  • Publisher Name: Humana Press

  • Print ISBN: 978-0-89603-822-6

  • Online ISBN: 978-1-59259-234-0

  • eBook Packages: Springer Protocols

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