Skip to main content
Erschienen in: Journal of Genetic Counseling 6/2014

01.12.2014 | Professional Issues

Genetic Information, Non-Discrimination, and Privacy Protections in Genetic Counseling Practice

verfasst von: Anya E. R. Prince, Myra I. Roche

Erschienen in: Journal of Genetic Counseling | Ausgabe 6/2014

Einloggen, um Zugang zu erhalten

Abstract

The passage of the Genetic Information Non Discrimination Act (GINA) was hailed as a pivotal achievement that was expected to calm the fears of both patients and research participants about the potential misuse of genetic information. However, 6 years later, patient and provider awareness of legal protections at both the federal and state level remains discouragingly low, thereby, limiting their potential effectiveness. The increasing demand for genetic testing will expand the number of individuals and families who could benefit from obtaining accurate information about the privacy and anti-discriminatory protections that GINA and other laws extend. In this paper we describe legal protections that are applicable to individuals seeking genetic counseling, review the literature on patient and provider fears of genetic discrimination and examine their awareness and understandings of existing laws, and summarize how genetic counselors currently discuss genetic discrimination. We then present three genetic counseling cases to illustrate issues of genetic discrimination and provide relevant information on applicable legal protections. Genetic counselors have an unprecedented opportunity, as well as the professional responsibility, to disseminate accurate knowledge about existing legal protections to their patients. They can strengthen their effectiveness in this role by achieving a greater knowledge of current protections including being able to identify specific steps that can help protect genetic information.
Fußnoten
1
This article presents general information about the law in order to educate genetic counselors about legal protections regarding genetic discrimination. It is not legal advice. Professional legal advice should always be sought before any legal action is taken. Application of the law may vary across situations because it is dependent on individually specific circumstances and on the applicable state and federal law.
 
Literatur
Zurück zum Zitat Ader, T., Susswein, L. R., Callanan, N. P., & Evans, J. P. (2009). Attitudes and practice of genetic counselors regarding anonymous testing for BRCA1/2. Journal of Genetic Counseling, 18(6), 606–617.PubMedCrossRef Ader, T., Susswein, L. R., Callanan, N. P., & Evans, J. P. (2009). Attitudes and practice of genetic counselors regarding anonymous testing for BRCA1/2. Journal of Genetic Counseling, 18(6), 606–617.PubMedCrossRef
Zurück zum Zitat Allain, D. C., Friedman, S., & Senter, L. (2012). Consumer awareness and attitudes about insurance discrimination post enactment of the genetic information Nondiscrimination Act. Familial Cancer, 11(4), 637–644.PubMedCrossRef Allain, D. C., Friedman, S., & Senter, L. (2012). Consumer awareness and attitudes about insurance discrimination post enactment of the genetic information Nondiscrimination Act. Familial Cancer, 11(4), 637–644.PubMedCrossRef
Zurück zum Zitat Americans with Disabilities Act of 1990 (ADA), Pub. L. 101-336. (1990). Americans with Disabilities Act of 1990 (ADA), Pub. L. 101-336. (1990).
Zurück zum Zitat Americans with Disabilities Act Amendments Act (ADAAA) of 2008, Pub. L. 110-325. (2008). Americans with Disabilities Act Amendments Act (ADAAA) of 2008, Pub. L. 110-325. (2008).
Zurück zum Zitat Association for Molecular Pathology (AMP) et al. v. Myriad Genetics, Inc. et al., 569 U.S. 12-398. (2013). Association for Molecular Pathology (AMP) et al. v. Myriad Genetics, Inc. et al., 569 U.S. 12-398. (2013).
Zurück zum Zitat Baruch, S., & Hudson, K. (2008). Civilian and military genetics: nondiscrimination policy in a Post-GINA World. The American Journal of Human Genetics, 83(4), 435–444.CrossRef Baruch, S., & Hudson, K. (2008). Civilian and military genetics: nondiscrimination policy in a Post-GINA World. The American Journal of Human Genetics, 83(4), 435–444.CrossRef
Zurück zum Zitat Bombard, Y., Palin, J., Friedman, J. M., Veenstra, G., Creighton, S., Bottorff, J. L., & Hayden, M. R. (2012). Beyond the patient: the broader impact of genetic discrimination among individuals at risk of Huntington disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B(2), 217–226.CrossRef Bombard, Y., Palin, J., Friedman, J. M., Veenstra, G., Creighton, S., Bottorff, J. L., & Hayden, M. R. (2012). Beyond the patient: the broader impact of genetic discrimination among individuals at risk of Huntington disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B(2), 217–226.CrossRef
Zurück zum Zitat Cal-GINA, Senate Bill No. 559. (2011). (codified in scattered sections of the California code). Cal-GINA, Senate Bill No. 559. (2011). (codified in scattered sections of the California code).
Zurück zum Zitat Code of Federal Regulations (CFR), Definitions Specific to GINA, 29 C.F.R. §1635.3. (2013). Code of Federal Regulations (CFR), Definitions Specific to GINA, 29 C.F.R. §1635.3. (2013).
Zurück zum Zitat Dorsey, E. R., Darwin, K. C., Nichols, P. E., Kwok, J. H., Bennet, C., Rosenthal, L. S., Bombard, Y., et al. (2013). Knowledge of the Genetic Information Nondiscrimination act among individuals affected by Huntington disease. Clinical Genetics, 84(3), 251–257.PubMedCrossRef Dorsey, E. R., Darwin, K. C., Nichols, P. E., Kwok, J. H., Bennet, C., Rosenthal, L. S., Bombard, Y., et al. (2013). Knowledge of the Genetic Information Nondiscrimination act among individuals affected by Huntington disease. Clinical Genetics, 84(3), 251–257.PubMedCrossRef
Zurück zum Zitat Genetic Information Nondiscrimination Act of 2008 (GINA), Pub. L. No. 110-233. (2008). (codified as amended in scattered sections of 26, 29, and 42 U.S.C.). Genetic Information Nondiscrimination Act of 2008 (GINA), Pub. L. No. 110-233. (2008). (codified as amended in scattered sections of 26, 29, and 42 U.S.C.).
Zurück zum Zitat Goh, A. M., Chiu, E., Yastrubetskaya, O., Erwin, C., Williams, J. K., Juhl, A. R., & Paulsen, J. S. (2013). Perception, experience, and response to genetic discrimination in Huntington’s disease: the Australian results of The International RESPOND-HD study. Genetic Testing and Molecular Biomarkers, 17(2), 115–121.PubMedCentralPubMedCrossRef Goh, A. M., Chiu, E., Yastrubetskaya, O., Erwin, C., Williams, J. K., Juhl, A. R., & Paulsen, J. S. (2013). Perception, experience, and response to genetic discrimination in Huntington’s disease: the Australian results of The International RESPOND-HD study. Genetic Testing and Molecular Biomarkers, 17(2), 115–121.PubMedCentralPubMedCrossRef
Zurück zum Zitat Guz v. Bechtel National, Inc., 24 Cal. 4th 317,8 P.3d 1089, 100 Cal. Rptr. 2d 352. (2000). Guz v. Bechtel National, Inc., 24 Cal. 4th 317,8 P.3d 1089, 100 Cal. Rptr. 2d 352. (2000).
Zurück zum Zitat Hadley, D. W., Jenkins, J., Dimond, E., Nakahara, K., Grogan, L., Liewehr, D. J., Steinberg, S. M., et al. (2003). Genetic counseling and testing in families with hereditary nonpolyposis colorectal cancer. Archives of Internal Medicine, 163(5), 573–582.PubMedCrossRef Hadley, D. W., Jenkins, J., Dimond, E., Nakahara, K., Grogan, L., Liewehr, D. J., Steinberg, S. M., et al. (2003). Genetic counseling and testing in families with hereditary nonpolyposis colorectal cancer. Archives of Internal Medicine, 163(5), 573–582.PubMedCrossRef
Zurück zum Zitat Haga, S., Barry, W., Mills, R., Ginsburg, G., Svetkey, L., Sullivan, J., & Willard, H. (2013). Public Knowledge of and attitudes toward genetics and genetic testing. Genetic Testing and Molecular Biomarkers, 17(4), 327–335.PubMedCentralPubMedCrossRef Haga, S., Barry, W., Mills, R., Ginsburg, G., Svetkey, L., Sullivan, J., & Willard, H. (2013). Public Knowledge of and attitudes toward genetics and genetic testing. Genetic Testing and Molecular Biomarkers, 17(4), 327–335.PubMedCentralPubMedCrossRef
Zurück zum Zitat Hall, M. A., & Rich, S. S. (2000). Patients’ fear of genetic discrimination by health insurers: the impact of legal protections. Genetics in Medicine, 2(4), 214–221.PubMedCrossRef Hall, M. A., & Rich, S. S. (2000). Patients’ fear of genetic discrimination by health insurers: the impact of legal protections. Genetics in Medicine, 2(4), 214–221.PubMedCrossRef
Zurück zum Zitat Hall, M. A., McEwen, J. E., Barton, J. C., Walker, A. P., Howe, E. G., Reiss, J. A., Power, T. E., et al. (2005). Concerns in a primary care population about genetic discrimination by insurers. Genetics in Medicine, 5(7), 745. Hall, M. A., McEwen, J. E., Barton, J. C., Walker, A. P., Howe, E. G., Reiss, J. A., Power, T. E., et al. (2005). Concerns in a primary care population about genetic discrimination by insurers. Genetics in Medicine, 5(7), 745.
Zurück zum Zitat Huang, M. Y., Huston, S. A., & Perri, M. (2013). Awareness of the US Genetic Information Nondiscrimination Act of 2008: an online survey. Journal of Pharmaceutical Health Services Research, 4(4), 235–238.CrossRef Huang, M. Y., Huston, S. A., & Perri, M. (2013). Awareness of the US Genetic Information Nondiscrimination Act of 2008: an online survey. Journal of Pharmaceutical Health Services Research, 4(4), 235–238.CrossRef
Zurück zum Zitat Jolie, A. (2013). My Medical Choices. The New York Times, p. A25. Jolie, A. (2013). My Medical Choices. The New York Times, p. A25.
Zurück zum Zitat Joly, Y., Feze, I. N., & Simard, J. (2013). Genetic discrimination and life insurance: a systematic review of the evidence. BMC Medicine, 11, 25.PubMedCentralPubMedCrossRef Joly, Y., Feze, I. N., & Simard, J. (2013). Genetic discrimination and life insurance: a systematic review of the evidence. BMC Medicine, 11, 25.PubMedCentralPubMedCrossRef
Zurück zum Zitat Kocarnik, J., & Fullerton, S. (2014). Returning pleiotropic results from genetic testing to patients and research participants. Journal of the American Medical Association, 311(8), 795–796.PubMedCentralPubMedCrossRef Kocarnik, J., & Fullerton, S. (2014). Returning pleiotropic results from genetic testing to patients and research participants. Journal of the American Medical Association, 311(8), 795–796.PubMedCentralPubMedCrossRef
Zurück zum Zitat Laedtke, A. L., O’Neill, S. M., Rubinstein, W. S., & Vogel, K. J. (2012). Family physicians’ awareness and knowledge of the Genetic Information Non-Discrimination Act (GINA). Journal of Genetic Counselin\g, 21(2), 345–352.CrossRef Laedtke, A. L., O’Neill, S. M., Rubinstein, W. S., & Vogel, K. J. (2012). Family physicians’ awareness and knowledge of the Genetic Information Non-Discrimination Act (GINA). Journal of Genetic Counselin\g, 21(2), 345–352.CrossRef
Zurück zum Zitat Lapham, E. V., Kozma, C., & Weiss, J. O. (1996). Genetic discrimination: perspectives of consumers. Science, 5287(274), 621–624.CrossRef Lapham, E. V., Kozma, C., & Weiss, J. O. (1996). Genetic discrimination: perspectives of consumers. Science, 5287(274), 621–624.CrossRef
Zurück zum Zitat Matloff, E. T., Shappell, H., Brierley, K., Bernhardt, B. A., McKinnon, W., & Peshkin, B. N. (2000). What would you do? Specialists’ perspectives on cancer genetic testing, prophylactic surgery, and insurance discrimination. Journal of Clinical Oncology, 12(18), 2484–2492. Matloff, E. T., Shappell, H., Brierley, K., Bernhardt, B. A., McKinnon, W., & Peshkin, B. N. (2000). What would you do? Specialists’ perspectives on cancer genetic testing, prophylactic surgery, and insurance discrimination. Journal of Clinical Oncology, 12(18), 2484–2492.
Zurück zum Zitat Matloff, E. T., Bonadies, D. C., Moyer, A., & Brierley, K. L. (2014). Changes in specialists’ perspectives on cancer genetic testing, prophylactic surgery and insurance discrimination: then and now. Journal of Genetic Counseling, 23(2), 164–171.PubMedCrossRef Matloff, E. T., Bonadies, D. C., Moyer, A., & Brierley, K. L. (2014). Changes in specialists’ perspectives on cancer genetic testing, prophylactic surgery and insurance discrimination: then and now. Journal of Genetic Counseling, 23(2), 164–171.PubMedCrossRef
Zurück zum Zitat New Jersey Code, NJS § 17B:30-12. (2008). New Jersey Code, NJS § 17B:30-12. (2008).
Zurück zum Zitat Pamarti, A. (2011). Genetic Information Nondiscrimination Act (GINA) and Its Affect on Genetic Counseling Practice: A Survey of Genetic Counselors. Unpublished Masters Thesis. Brandies University, Massachusetts. Pamarti, A. (2011). Genetic Information Nondiscrimination Act (GINA) and Its Affect on Genetic Counseling Practice: A Survey of Genetic Counselors. Unpublished Masters Thesis. Brandies University, Massachusetts.
Zurück zum Zitat Patient Protection and Affordable Care Act, 42 U.S.C. § 18001 et seq. (2010). Patient Protection and Affordable Care Act, 42 U.S.C. § 18001 et seq. (2010).
Zurück zum Zitat Pollitz, K., Peshkin, B. N., Bangit, E., & Lucia, K. (2007). Genetic discrimination in health insurance: current legal protections and industry practices. Inquiry, 44(3), 350–368.PubMed Pollitz, K., Peshkin, B. N., Bangit, E., & Lucia, K. (2007). Genetic discrimination in health insurance: current legal protections and industry practices. Inquiry, 44(3), 350–368.PubMed
Zurück zum Zitat Prince, A. (2012). Genetic information and medical records – a cautionary tale for patients, healthcare professionals, and insurance companies. Health Lawyer, 5(24), 29–33. Prince, A. (2012). Genetic information and medical records – a cautionary tale for patients, healthcare professionals, and insurance companies. Health Lawyer, 5(24), 29–33.
Zurück zum Zitat Rothstein, M. A. (2008). GINA, the ADA, and genetic discrimination in employment. Journal of Law, Medicine, & Ethics, 36(4), 837–840.CrossRef Rothstein, M. A. (2008). GINA, the ADA, and genetic discrimination in employment. Journal of Law, Medicine, & Ethics, 36(4), 837–840.CrossRef
Zurück zum Zitat Sharpe, N. F., & Carter, R. F. (2006). Genetic testing: Care, consent, and liability (p. 153). New Jersey: John Wiley & Sons. Sharpe, N. F., & Carter, R. F. (2006). Genetic testing: Care, consent, and liability (p. 153). New Jersey: John Wiley & Sons.
Zurück zum Zitat Equal Employment Opportunity Commission (EEOC) – Where individuals must file a complaint of employment discrimination. Equal Employment Opportunity Commission (EEOC) – Where individuals must file a complaint of employment discrimination.
Zurück zum Zitat Cancer Legal Resource Center – Organization has a free national telephone assistance line where patients can ask questions about cancer and genetic-related legal issues. Cancer Legal Resource Center – Organization has a free national telephone assistance line where patients can ask questions about cancer and genetic-related legal issues.
Zurück zum Zitat Patient Advocate Foundation – Organization offers assistance with insurance appeals as well as general resources for patients. Patient Advocate Foundation – Organization offers assistance with insurance appeals as well as general resources for patients.
Metadaten
Titel
Genetic Information, Non-Discrimination, and Privacy Protections in Genetic Counseling Practice
verfasst von
Anya E. R. Prince
Myra I. Roche
Publikationsdatum
01.12.2014
Verlag
Springer US
Erschienen in
Journal of Genetic Counseling / Ausgabe 6/2014
Print ISSN: 1059-7700
Elektronische ISSN: 1573-3599
DOI
https://doi.org/10.1007/s10897-014-9743-2

Weitere Artikel der Ausgabe 6/2014

Journal of Genetic Counseling 6/2014 Zur Ausgabe

Update Gynäkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert – ganz bequem per eMail.