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Published in: Journal of Genetic Counseling 4/2014

01-08-2014 | Professional Issues

Genomic Counseling: Next Generation Counseling

Authors: Rachel Mills, Susanne B. Haga

Published in: Journal of Genetic Counseling | Issue 4/2014

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Abstract

Personalized medicine continues to expand with the development and increasing use of genome-based testing. While these advances present new opportunities for diagnosis and risk assessment, they also present challenges to clinical delivery. Genetic counselors will play an important role in ushering in this new era of testing; however, it will warrant a shift from traditional genetic counseling to “genomic counseling.” This shift will be marked by a move from reactive genetic testing for diagnosis of primarily single-gene diseases to proactive genome-based testing for multiple complex diseases for the purpose of disease prevention. It will also require discussion of risk information for a number of diseases, some of which may have low relative risks or weak associations, and thus, may not substantially impact clinical care. Additionally, genomic counselors will expand their roles, particularly in the area of health promotion to reduce disease risk. This additional role will require a style of counseling that is more directive than traditional counseling and require greater knowledge about risk reducing behaviors and disease screening.
Literature
go back to reference Amrhein, P. C., Miller, W. R., Yahne, C. E., Palmer, M., & Fulcher, L. (2003). Client commitment language during motivational interviewing predicts drug use outcomes. Journal of Consulting and Clinical Psychology, 71(5), 12.CrossRef Amrhein, P. C., Miller, W. R., Yahne, C. E., Palmer, M., & Fulcher, L. (2003). Client commitment language during motivational interviewing predicts drug use outcomes. Journal of Consulting and Clinical Psychology, 71(5), 12.CrossRef
go back to reference Ashley, E. A., Butte, A. J., Wheeler, M. T., Chen, R., Klein, T. E., Dewey, F. E., et al. (2010). Clinical assessment incorporating a personal genome. Lancet, 375(9725), 1525–1535.CrossRef Ashley, E. A., Butte, A. J., Wheeler, M. T., Chen, R., Klein, T. E., Dewey, F. E., et al. (2010). Clinical assessment incorporating a personal genome. Lancet, 375(9725), 1525–1535.CrossRef
go back to reference Baker, D. L., Schuette, J. L., & Uhlmann, W. R. (1998). A guide to genetic counseling. New York: Wiley-Liss. Baker, D. L., Schuette, J. L., & Uhlmann, W. R. (1998). A guide to genetic counseling. New York: Wiley-Liss.
go back to reference Battista, R. N., Blancquaert, I., Laberge, A. M., van Schendel, N., & Leduc, N. (2012). Genetics in health care: an overview of current and emerging models. Public health genomics, 15(1), 34–45.CrossRef Battista, R. N., Blancquaert, I., Laberge, A. M., van Schendel, N., & Leduc, N. (2012). Genetics in health care: an overview of current and emerging models. Public health genomics, 15(1), 34–45.CrossRef
go back to reference Biesecker, B. B. (2001). Goals of genetic counseling. Clinical genetics, 60(5), 323–330.CrossRef Biesecker, B. B. (2001). Goals of genetic counseling. Clinical genetics, 60(5), 323–330.CrossRef
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.CrossRef 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.CrossRef
go back to reference Chan, I. S., & Ginsburg, G. S. (2011). Personalized medicine: progress and promise. Annual review of genomics and human genetics, 12, 217–244.CrossRef Chan, I. S., & Ginsburg, G. S. (2011). Personalized medicine: progress and promise. Annual review of genomics and human genetics, 12, 217–244.CrossRef
go back to reference Corpas, M. (2012). A family experience of personal genomics. Journal of genetic counseling, 21(3), 386–391.CrossRef Corpas, M. (2012). A family experience of personal genomics. Journal of genetic counseling, 21(3), 386–391.CrossRef
go back to reference Darst, B., Madlensky, L., Schork, N., Topol, E., Bloss, C. (2013). Perceptions of genetic counseling services in direct-to-consumer personal genomic testing. Clinical genetics.CrossRef Darst, B., Madlensky, L., Schork, N., Topol, E., Bloss, C. (2013). Perceptions of genetic counseling services in direct-to-consumer personal genomic testing. Clinical genetics.CrossRef
go back to reference Florez, J. C., Jablonski, K. A., Bayley, N., Pollin, T. I., de Bakker, P. I., Shuldiner, A. R., et al. (2006). TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program. The New England journal of medicine, 355(3), 241–250.CrossRef Florez, J. C., Jablonski, K. A., Bayley, N., Pollin, T. I., de Bakker, P. I., Shuldiner, A. R., et al. (2006). TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program. The New England journal of medicine, 355(3), 241–250.CrossRef
go back to reference Gettig, E. (2010). Commentary on genome-guided preventive medicine-new roles for genetic counselors. Journal of genetic counseling, 19(4), 328–329.CrossRef Gettig, E. (2010). Commentary on genome-guided preventive medicine-new roles for genetic counselors. Journal of genetic counseling, 19(4), 328–329.CrossRef
go back to reference Gordon, E. S., Griffin, G., Wawak, L., Pang, H., Gollust, S. E., & Bernhardt, B. A. (2012). "It's Not Like Judgment Day": Public Understanding of and Reactions to Personalized Genomic Risk Information. Journal of genetic counseling, 21(3), 423–432.CrossRef Gordon, E. S., Griffin, G., Wawak, L., Pang, H., Gollust, S. E., & Bernhardt, B. A. (2012). "It's Not Like Judgment Day": Public Understanding of and Reactions to Personalized Genomic Risk Information. Journal of genetic counseling, 21(3), 423–432.CrossRef
go back to reference Haga, S. B. (2009). Ethical issues of predictive genetic testing for diabetes. Journal of diabetes science and technology, 3(4), 781–788.CrossRef Haga, S. B. (2009). Ethical issues of predictive genetic testing for diabetes. Journal of diabetes science and technology, 3(4), 781–788.CrossRef
go back to reference Haga, S. B., Burke, W., Ginsburg, G. S., Mills, R., & Agans, R. (2012). Primary care physicians' knowledge of and experience with pharmacogenetic testing. Clinical genetics, 82(4), 388–394.CrossRef Haga, S. B., Burke, W., Ginsburg, G. S., Mills, R., & Agans, R. (2012). Primary care physicians' knowledge of and experience with pharmacogenetic testing. Clinical genetics, 82(4), 388–394.CrossRef
go back to reference Heshka, J. T., Palleschi, C., Howley, H., Wilson, B., & Wells, P. S. (2008). A systematic review of perceived risks, psychological and behavioral impacts of genetic testing. Genetics in medicine : official journal of the American College of Medical Genetics, 10(1), 19–32.CrossRef Heshka, J. T., Palleschi, C., Howley, H., Wilson, B., & Wells, P. S. (2008). A systematic review of perceived risks, psychological and behavioral impacts of genetic testing. Genetics in medicine : official journal of the American College of Medical Genetics, 10(1), 19–32.CrossRef
go back to reference Hettema, J., Steele, J., & Miller, W. R. (2005). Motivational interviewing. Annu Rev Clin Psychol, 1, 91–111.CrossRef Hettema, J., Steele, J., & Miller, W. R. (2005). Motivational interviewing. Annu Rev Clin Psychol, 1, 91–111.CrossRef
go back to reference Hofman, K. J., Tambor, E. S., Chase, G. A., Geller, G., Faden, R. R., & Holtzman, N. A. (1993). Physicians' knowledge of genetics and genetic tests. Academic medicine : journal of the Association of American Medical Colleges, 68(8), 625–632.CrossRef Hofman, K. J., Tambor, E. S., Chase, G. A., Geller, G., Faden, R. R., & Holtzman, N. A. (1993). Physicians' knowledge of genetics and genetic tests. Academic medicine : journal of the Association of American Medical Colleges, 68(8), 625–632.CrossRef
go back to reference Hunter, A., Wright, P., Cappelli, M., Kasaboski, A., & Surh, L. (1998). Physician knowledge and attitudes towards molecular genetic (DNA) testing of their patients. Clinical genetics, 53(6), 447–455.CrossRef Hunter, A., Wright, P., Cappelli, M., Kasaboski, A., & Surh, L. (1998). Physician knowledge and attitudes towards molecular genetic (DNA) testing of their patients. Clinical genetics, 53(6), 447–455.CrossRef
go back to reference Levin, E., Riordan, S., Klein, J., & Kieran, S. (2012). Genetic counseling for personal genomic testing: optimizing client uptake of post-test telephonic counseling services. Journal of genetic counseling, 21(3), 462–468.CrossRef Levin, E., Riordan, S., Klein, J., & Kieran, S. (2012). Genetic counseling for personal genomic testing: optimizing client uptake of post-test telephonic counseling services. Journal of genetic counseling, 21(3), 462–468.CrossRef
go back to reference Markowitz, S. M., Park, E. R., Delahanty, L. M., O'Brien, K. E., & Grant, R. W. (2011). Perceived impact of diabetes genetic risk testing among patients at high phenotypic risk for type 2 diabetes. Diabetes care, 34(3), 568–573.CrossRef Markowitz, S. M., Park, E. R., Delahanty, L. M., O'Brien, K. E., & Grant, R. W. (2011). Perceived impact of diabetes genetic risk testing among patients at high phenotypic risk for type 2 diabetes. Diabetes care, 34(3), 568–573.CrossRef
go back to reference Marteau, T. M., French, D. P., Griffin, S. J., Prevost, A. T., Sutton, S., Watkinson, C., et al. (2010). Effects of communicating DNA-based disease risk estimates on risk-reducing behaviours. Cochrane Database Syst Rev, 10, CD007275. Marteau, T. M., French, D. P., Griffin, S. J., Prevost, A. T., Sutton, S., Watkinson, C., et al. (2010). Effects of communicating DNA-based disease risk estimates on risk-reducing behaviours. Cochrane Database Syst Rev, 10, CD007275.
go back to reference Marteau, T. M., & Lerman, C. (2001). Genetic risk and behavioural change. BMJ, 322(7293), 1056–1059.CrossRef Marteau, T. M., & Lerman, C. (2001). Genetic risk and behavioural change. BMJ, 322(7293), 1056–1059.CrossRef
go back to reference Mattei, J., Qi, Q., Hu, F. B., Sacks, F. M., & Qi, L. (2012). TCF7L2 genetic variants modulate the effect of dietary fat intake on changes in body composition during a weight-loss intervention. The American journal of clinical nutrition, 96(5), 1129–1136.CrossRef Mattei, J., Qi, Q., Hu, F. B., Sacks, F. M., & Qi, L. (2012). TCF7L2 genetic variants modulate the effect of dietary fat intake on changes in body composition during a weight-loss intervention. The American journal of clinical nutrition, 96(5), 1129–1136.CrossRef
go back to reference McCaffery, J. M., Jablonski, K. A., Franks, P. W., Dagogo-Jack, S., Wing, R. R., Knowler, W. C., et al. (2011). TCF7L2 polymorphism, weight loss and proinsulin:insulin ratio in the diabetes prevention program. PloS one, 6(7), e21518.CrossRef McCaffery, J. M., Jablonski, K. A., Franks, P. W., Dagogo-Jack, S., Wing, R. R., Knowler, W. C., et al. (2011). TCF7L2 polymorphism, weight loss and proinsulin:insulin ratio in the diabetes prevention program. PloS one, 6(7), e21518.CrossRef
go back to reference Middleton, A. (2012). Communication about DTC testing: commentary on a 'family experience of personal genomics'. Journal of genetic counseling, 21(3), 392–398.CrossRef Middleton, A. (2012). Communication about DTC testing: commentary on a 'family experience of personal genomics'. Journal of genetic counseling, 21(3), 392–398.CrossRef
go back to reference O'Daniel, J. M. (2010). The prospect of genome-guided preventive medicine: a need and opportunity for genetic counselors. Journal of genetic counseling, 19(4), 315–327.CrossRef O'Daniel, J. M. (2010). The prospect of genome-guided preventive medicine: a need and opportunity for genetic counselors. Journal of genetic counseling, 19(4), 315–327.CrossRef
go back to reference Ormond, K. E., Wheeler, M. T., Hudgins, L., Klein, T. E., Butte, A. J., Altman, R. B., et al. (2010). Challenges in the clinical application of whole-genome sequencing. Lancet, 375(9727), 1749–1751.CrossRef Ormond, K. E., Wheeler, M. T., Hudgins, L., Klein, T. E., Butte, A. J., Altman, R. B., et al. (2010). Challenges in the clinical application of whole-genome sequencing. Lancet, 375(9727), 1749–1751.CrossRef
go back to reference Patel, C. J., Sivadas, A., Tabassum, R., Preeprem, T., Zhao, J., Arafat, D., et al. (2013). Whole Genome Sequencing in support of Wellness and Health Maintenance. Genome medicine, 5(6), 58.CrossRef Patel, C. J., Sivadas, A., Tabassum, R., Preeprem, T., Zhao, J., Arafat, D., et al. (2013). Whole Genome Sequencing in support of Wellness and Health Maintenance. Genome medicine, 5(6), 58.CrossRef
go back to reference Pengchit, W., Walters, S. T., Simmons, R. G., Kohlmann, W., Burt, R. W., Schwartz, M. D., et al. (2011). Motivation-based intervention to promote colonoscopy screening: an integration of a fear management model and motivational interviewing. Journal of health psychology, 16(8), 1187–1197.CrossRef Pengchit, W., Walters, S. T., Simmons, R. G., Kohlmann, W., Burt, R. W., Schwartz, M. D., et al. (2011). Motivation-based intervention to promote colonoscopy screening: an integration of a fear management model and motivational interviewing. Journal of health psychology, 16(8), 1187–1197.CrossRef
go back to reference Peter, I., McCaffery, J. M., Kelley-Hedgepeth, A., Hakonarson, H., Reis, S., Wagenknecht, L. E., et al. (2012). Association of type 2 diabetes susceptibility loci with one-year weight loss in the look AHEAD clinical trial. Obesity, 20(8), 1675–1682.CrossRef Peter, I., McCaffery, J. M., Kelley-Hedgepeth, A., Hakonarson, H., Reis, S., Wagenknecht, L. E., et al. (2012). Association of type 2 diabetes susceptibility loci with one-year weight loss in the look AHEAD clinical trial. Obesity, 20(8), 1675–1682.CrossRef
go back to reference Phimister, E. G., Feero, W. G., & Guttmacher, A. E. (2012). Realizing genomic medicine. The New England journal of medicine, 366(8), 757–759.CrossRef Phimister, E. G., Feero, W. G., & Guttmacher, A. E. (2012). Realizing genomic medicine. The New England journal of medicine, 366(8), 757–759.CrossRef
go back to reference Pierce, M., Ridout, D., Harding, D., Keen, H., & Bradley, C. (2000). More good than harm: a randomised controlled trial of the effect of education about familial risk of diabetes on psychological outcomes. Br J Gen Pract, 50(460), 867–871.PubMedPubMedCentral Pierce, M., Ridout, D., Harding, D., Keen, H., & Bradley, C. (2000). More good than harm: a randomised controlled trial of the effect of education about familial risk of diabetes on psychological outcomes. Br J Gen Pract, 50(460), 867–871.PubMedPubMedCentral
go back to reference Riordan, S., Rodriguez, D. F., Kieran, S. (2012). Personal Genomic Testing as Part of the Complete Breast Cancer Risk Assessment: A Case Report. Journal of genetic counseling. Riordan, S., Rodriguez, D. F., Kieran, S. (2012). Personal Genomic Testing as Part of the Complete Breast Cancer Risk Assessment: A Case Report. Journal of genetic counseling.
go back to reference Roberts, M. E., Riegert-Johnson, D. L., & Thomas, B. C. (2011). Self diagnosis of Lynch syndrome using direct to consumer genetic testing: a case study. Journal of genetic counseling, 20(4), 327–329.CrossRef Roberts, M. E., Riegert-Johnson, D. L., & Thomas, B. C. (2011). Self diagnosis of Lynch syndrome using direct to consumer genetic testing: a case study. Journal of genetic counseling, 20(4), 327–329.CrossRef
go back to reference Scheuner, M. T., Sieverding, P., & Shekelle, P. G. (2008). Delivery of genomic medicine for common chronic adult diseases: a systematic review. JAMA : the journal of the American Medical Association, 299(11), 1320–1334.CrossRef Scheuner, M. T., Sieverding, P., & Shekelle, P. G. (2008). Delivery of genomic medicine for common chronic adult diseases: a systematic review. JAMA : the journal of the American Medical Association, 299(11), 1320–1334.CrossRef
go back to reference Sharp, R. R. (2011). Downsizing genomic medicine: approaching the ethical complexity of whole-genome sequencing by starting small. Genetics in medicine : official journal of the American College of Medical Genetics, 13(3), 191–194.CrossRef Sharp, R. R. (2011). Downsizing genomic medicine: approaching the ethical complexity of whole-genome sequencing by starting small. Genetics in medicine : official journal of the American College of Medical Genetics, 13(3), 191–194.CrossRef
go back to reference Sturm, A. C., Manickam, K. (2012). Direct-to-Consumer Personal Genomic Testing: A Case Study and Practical Recommendations for "Genomic Counseling". Journal of genetic counseling. Sturm, A. C., Manickam, K. (2012). Direct-to-Consumer Personal Genomic Testing: A Case Study and Practical Recommendations for "Genomic Counseling". Journal of genetic counseling.
go back to reference Waxler, J. L., O'Brien, K. E., Delahanty, L. M., Meigs, J. B., Florez, J. C., Park, E. R. et al. (2012) Genetic Counseling as a Tool for Type 2 Diabetes Prevention: A Genetic Counseling Framework for Common Polygenetic Disorders. Journal of genetic counseling. Waxler, J. L., O'Brien, K. E., Delahanty, L. M., Meigs, J. B., Florez, J. C., Park, E. R. et al. (2012) Genetic Counseling as a Tool for Type 2 Diabetes Prevention: A Genetic Counseling Framework for Common Polygenetic Disorders. Journal of genetic counseling.
go back to reference Zhang, X., Qi, Q., Zhang, C., Smith, S. R., Hu, F. B., Sacks, F. M., et al. (2012). FTO genotype and 2-year change in body composition and fat distribution in response to weight-loss diets: the POUNDS LOST Trial. Diabetes, 61(11), 3005–3011.CrossRef Zhang, X., Qi, Q., Zhang, C., Smith, S. R., Hu, F. B., Sacks, F. M., et al. (2012). FTO genotype and 2-year change in body composition and fat distribution in response to weight-loss diets: the POUNDS LOST Trial. Diabetes, 61(11), 3005–3011.CrossRef
Metadata
Title
Genomic Counseling: Next Generation Counseling
Authors
Rachel Mills
Susanne B. Haga
Publication date
01-08-2014
Publisher
Springer US
Published in
Journal of Genetic Counseling / Issue 4/2014
Print ISSN: 1059-7700
Electronic ISSN: 1573-3599
DOI
https://doi.org/10.1007/s10897-013-9641-z

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