Skip to main content
Top
Published in: Journal of Genetic Counseling 3/2012

01-06-2012 | Professional Issues

Direct-to-Consumer Genetic Testing: What Are We Talking About?

Authors: Meredith Weaver, Toni I. Pollin

Published in: Journal of Genetic Counseling | Issue 3/2012

Login to get access

Abstract

The term Direct-to-Consumer (DTC) genetic testing refers to many different categories of testing. This editorial addresses the issues related to DTC testing for large effect and small effect variants associated with disease. In particular, there are issues of clinical validity and utility, informativeness and residual risk. Genetic counselors are poised to address these issues because of their training in probability and statistical models. The authors suggest that genetic counselors can impact the general public’s understanding of DTC test results by: including evaluation of DTC concepts in graduate program curricula, holding AEC plenary sessions about emerging DTC concepts, and helping other professionals understand DTC concepts. Importantly, genetic counselors are advised to continue doing and promoting rigorous research on how people access and use DTC genetic testing and results, as well as gathering empirical data so that discussions of harms and benefits can go beyond theory. It is our hope that genetic counselors in practice will continue to critically evaluate claims made about emerging new tests, including those marketed DTC, in order to provide the best possible services to our patients.
Literature
go back to reference Ahlqvist, E., Ahluwalia, T. S., & Groop, L. (2011). Genetics of type 2 diabetes. Clinical Chemistry, 57(2), 241–254.PubMedCrossRef Ahlqvist, E., Ahluwalia, T. S., & Groop, L. (2011). Genetics of type 2 diabetes. Clinical Chemistry, 57(2), 241–254.PubMedCrossRef
go back to reference Antoniou, A., Pharoah, P. D., Narod, S., Risch, H. A., Eyfjord, J. E., Hopper, J. L., et al. (2003). Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies. American Journal of Human Genetics, 72(5), 1117–1130.PubMedCrossRef Antoniou, A., Pharoah, P. D., Narod, S., Risch, H. A., Eyfjord, J. E., Hopper, J. L., et al. (2003). Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies. American Journal of Human Genetics, 72(5), 1117–1130.PubMedCrossRef
go back to reference Bloss, C. S., Schork, N. J., & Topol, E. J. (2011). Effect of direct-to-consumer genomewide profiling to assess disease risk. The New England Journal of Medicine, 364(6), 524–534.PubMedCrossRef Bloss, C. S., Schork, N. J., & Topol, E. J. (2011). Effect of direct-to-consumer genomewide profiling to assess disease risk. The New England Journal of Medicine, 364(6), 524–534.PubMedCrossRef
go back to reference Blumenthal, D., Causino, N., Chang, Y. C., Culpepper, L., Marder, W., Saglam, D., et al. (1999). The duration of ambulatory visits to physicians. The Journal of Family Practice, 48(4), 264–271.PubMed Blumenthal, D., Causino, N., Chang, Y. C., Culpepper, L., Marder, W., Saglam, D., et al. (1999). The duration of ambulatory visits to physicians. The Journal of Family Practice, 48(4), 264–271.PubMed
go back to reference Burke, W., Culver, J. O., Bowen, D., Lowry, D., Durfy, S., McTiernan, A., & Andersen, M. R. (2000). Genetic counseling for women with an intermediate family history of breast cancer. American Journal of Medical Genetics, 90(5), 361–368.PubMedCrossRef Burke, W., Culver, J. O., Bowen, D., Lowry, D., Durfy, S., McTiernan, A., & Andersen, M. R. (2000). Genetic counseling for women with an intermediate family history of breast cancer. American Journal of Medical Genetics, 90(5), 361–368.PubMedCrossRef
go back to reference Giardiello, F. M., Brensinger, J. D., Petersen, G. M., Luce, M. C., Hylind, L. M., Bacon, J. A., et al. (1997). The use and interpretation of commercial APC gene testing for familial adenomatous polyposis. The New England Journal of Medicine, 336(12), 823–827.PubMedCrossRef Giardiello, F. M., Brensinger, J. D., Petersen, G. M., Luce, M. C., Hylind, L. M., Bacon, J. A., et al. (1997). The use and interpretation of commercial APC gene testing for familial adenomatous polyposis. The New England Journal of Medicine, 336(12), 823–827.PubMedCrossRef
go back to reference Grosse, S. D., Boyle, C. A., Botkin, J. R., Comeau, A. M., Kharrazi, M., Rosenfeld, M., et al. (2004). Newborn screening for cystic fibrosis: evaluation of benefits and risks and recommendations for state newborn screening programs. MMWR Recommendations and Reports: Morbidity and Mortality Weekly Report Recommendations and Reports/Centers for Disease Control, 53(RR-13), 1–36. Grosse, S. D., Boyle, C. A., Botkin, J. R., Comeau, A. M., Kharrazi, M., Rosenfeld, M., et al. (2004). Newborn screening for cystic fibrosis: evaluation of benefits and risks and recommendations for state newborn screening programs. MMWR Recommendations and Reports: Morbidity and Mortality Weekly Report Recommendations and Reports/Centers for Disease Control, 53(RR-13), 1–36.
go back to reference Grosse, S. D., & Khoury, M. J. (2006). What is the clinical utility of genetic testing? Genetics in Medicine: Official Journal of the American College of Medical Genetics, 8(7), 448–450. Grosse, S. D., & Khoury, M. J. (2006). What is the clinical utility of genetic testing? Genetics in Medicine: Official Journal of the American College of Medical Genetics, 8(7), 448–450.
go back to reference Hayat Roshanai, A., Rosenquist, R., Lampic, C., & Nordin, K. (2009). Cancer genetic counselees' self-reported psychological distress, changes in life, and adherence to recommended surveillance programs 3–7 years post counseling. Journal of Genetic Counseling, 18(2), 185–194.PubMedCrossRef Hayat Roshanai, A., Rosenquist, R., Lampic, C., & Nordin, K. (2009). Cancer genetic counselees' self-reported psychological distress, changes in life, and adherence to recommended surveillance programs 3–7 years post counseling. Journal of Genetic Counseling, 18(2), 185–194.PubMedCrossRef
go back to reference Hock, K. T., Christensen, K. D., Yashar, B. M., Roberts, J. S., Gollust, S. E., & Uhlmann, W. R. (2011). Direct-to-consumer genetic testing: an assessment of genetic counselors’ knowledge and beliefs. Genetics in Medicine: Official Journal of the American College of Medical Genetics, 13(4), 325–332. Hock, K. T., Christensen, K. D., Yashar, B. M., Roberts, J. S., Gollust, S. E., & Uhlmann, W. R. (2011). Direct-to-consumer genetic testing: an assessment of genetic counselors’ knowledge and beliefs. Genetics in Medicine: Official Journal of the American College of Medical Genetics, 13(4), 325–332.
go back to reference Lerman, C., Lustbader, E., Rimer, B., Daly, M., Miller, S., Sands, C., & Balshem, A. (1995). Effects of individualized breast cancer risk counseling: a randomized trial. Journal of the National Cancer Institute, 87(4), 286–292.PubMedCrossRef Lerman, C., Lustbader, E., Rimer, B., Daly, M., Miller, S., Sands, C., & Balshem, A. (1995). Effects of individualized breast cancer risk counseling: a randomized trial. Journal of the National Cancer Institute, 87(4), 286–292.PubMedCrossRef
go back to reference Maher, B. (2008). Personal genomes: the case of the missing heritability. Nature, 456(7218), 18–21.PubMedCrossRef Maher, B. (2008). Personal genomes: the case of the missing heritability. Nature, 456(7218), 18–21.PubMedCrossRef
go back to reference Mihaescu, R., Meigs, J., Sijbrands, E., & Janssens, A. C. (2011). Genetic risk profiling for prediction of type 2 diabetes. PLoS Currents, 3, RRN1208.PubMedCrossRef Mihaescu, R., Meigs, J., Sijbrands, E., & Janssens, A. C. (2011). Genetic risk profiling for prediction of type 2 diabetes. PLoS Currents, 3, RRN1208.PubMedCrossRef
go back to reference Myers, M. F., Chang, M. H., Jorgensen, C., Whitworth, W., Kassim, S., Litch, J. A., et al. (2006). Genetic testing for susceptibility to breast and ovarian cancer: evaluating the impact of a direct-to-consumer marketing campaign on physicians' knowledge and practices. Genetics in Medicine: Official Journal of the American College of Medical Genetics, 8(6), 361–370. Myers, M. F., Chang, M. H., Jorgensen, C., Whitworth, W., Kassim, S., Litch, J. A., et al. (2006). Genetic testing for susceptibility to breast and ovarian cancer: evaluating the impact of a direct-to-consumer marketing campaign on physicians' knowledge and practices. Genetics in Medicine: Official Journal of the American College of Medical Genetics, 8(6), 361–370.
go back to reference Pinto, D., Darvishi, K., Shi, X., Rajan, D., Rigler, D., Fitzgerald, T., et al. (2011). Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants. Nature Biotechnology, 29(6), 512–520.PubMedCrossRef Pinto, D., Darvishi, K., Shi, X., Rajan, D., Rigler, D., Fitzgerald, T., et al. (2011). Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants. Nature Biotechnology, 29(6), 512–520.PubMedCrossRef
go back to reference Sivell, S., Elwyn, G., Gaff, C. L., Clarke, A. J., Iredale, R., Shaw, C., et al. (2008). How risk is perceived, constructed and interpreted by clients in clinical genetics, and the effects on decision making: systematic review. Journal of Genetic Counseling, 17(1), 30–63.PubMedCrossRef Sivell, S., Elwyn, G., Gaff, C. L., Clarke, A. J., Iredale, R., Shaw, C., et al. (2008). How risk is perceived, constructed and interpreted by clients in clinical genetics, and the effects on decision making: systematic review. Journal of Genetic Counseling, 17(1), 30–63.PubMedCrossRef
go back to reference Voight, B. F., Scott, L. J., Steinthorsdottir, V., Morris, A. P., Dina, C., Welch, R. P., et al. (2010). Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nature Genetics, 42(7), 579–589.PubMedCrossRef Voight, B. F., Scott, L. J., Steinthorsdottir, V., Morris, A. P., Dina, C., Welch, R. P., et al. (2010). Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nature Genetics, 42(7), 579–589.PubMedCrossRef
go back to reference Watson, M., Lloyd, S., Davidson, J., Meyer, L., Eeles, R., Ebbs, S., & Murday, V. (1999). The impact of genetic counselling on risk perception and mental health in women with a family history of breast cancer. British Journal of Cancer, 79(5–6), 868–874.PubMedCrossRef Watson, M., Lloyd, S., Davidson, J., Meyer, L., Eeles, R., Ebbs, S., & Murday, V. (1999). The impact of genetic counselling on risk perception and mental health in women with a family history of breast cancer. British Journal of Cancer, 79(5–6), 868–874.PubMedCrossRef
go back to reference Wroe, A. L., Salkovskis, P. M., & Rimes, K. A. (1998). The prospect of predictive testing for personal risk: attitudes and decision making. Behaviour Research and Therapy, 36(6), 599–619.PubMedCrossRef Wroe, A. L., Salkovskis, P. M., & Rimes, K. A. (1998). The prospect of predictive testing for personal risk: attitudes and decision making. Behaviour Research and Therapy, 36(6), 599–619.PubMedCrossRef
Metadata
Title
Direct-to-Consumer Genetic Testing: What Are We Talking About?
Authors
Meredith Weaver
Toni I. Pollin
Publication date
01-06-2012
Publisher
Springer US
Published in
Journal of Genetic Counseling / Issue 3/2012
Print ISSN: 1059-7700
Electronic ISSN: 1573-3599
DOI
https://doi.org/10.1007/s10897-012-9493-y

Other articles of this Issue 3/2012

Journal of Genetic Counseling 3/2012 Go to the issue