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Published in: Journal of Genetic Counseling 4/2014

01-08-2014 | Next Generation Genetic Counseling

Assessing the Integration of Genomic Medicine in Genetic Counseling Training Programs

Authors: Jessica Profato, Erynn S. Gordon, Shannan Dixon, Andrea Kwan

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

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Abstract

Medical genetics has entered a period of transition from genetics to genomics. Genetic counselors (GCs) may take on roles in the clinical implementation of genomics. This study explores the perspectives of program directors (PDs) on including genomic medicine in GC training programs, as well as the status of this integration. Study methods included an online survey, an optional one-on-one telephone interview, and an optional curricula content analysis. The majority of respondents (15/16) reported that it is important to include genomic medicine in program curricula. Most topics of genomic medicine are either “currently taught” or “under development” in all participating programs. Interview data from five PDs and one faculty member supported the survey data. Integrating genomics in training programs is challenging, and it is essential to develop genomics resources for curricula.
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Literature
go back to reference Bernhardt, B. A., Zayac, C., Gordon, E. S., Wawak, L., Pyeritz, R. E., & Gollust, S. E. (2012). Incorporating direct-to consumer genomic information into patient care: attitudes and experiences of primary care physicians. Personalized Medicine, 9(7), 683–692.PubMedPubMedCentralCrossRef Bernhardt, B. A., Zayac, C., Gordon, E. S., Wawak, L., Pyeritz, R. E., & Gollust, S. E. (2012). Incorporating direct-to consumer genomic information into patient care: attitudes and experiences of primary care physicians. Personalized Medicine, 9(7), 683–692.PubMedPubMedCentralCrossRef
go back to reference Billings, L. K., & Florez, J. C. (2010). The genetics of type 2 diabetes: what have we learned from GWAS? Annals of the New York Academy of Sciences, 1212, 59–77.PubMedPubMedCentralCrossRef Billings, L. K., & Florez, J. C. (2010). The genetics of type 2 diabetes: what have we learned from GWAS? Annals of the New York Academy of Sciences, 1212, 59–77.PubMedPubMedCentralCrossRef
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.PubMedCrossRef Chan, I. S., & Ginsburg, G. S. (2011). Personalized medicine: progress and promise. Annual Review of Genomics and Human Genetics, 12, 217–244.PubMedCrossRef
go back to reference Collins, F. S., & Guttmacher, A. E. (2001). Genetics moves into the medical mainstream. Journal of the American Medical Association, 286(18), 2322–2324.PubMedCrossRef Collins, F. S., & Guttmacher, A. E. (2001). Genetics moves into the medical mainstream. Journal of the American Medical Association, 286(18), 2322–2324.PubMedCrossRef
go back to reference Ginsburg, G. S., & Willard, H. F. (2009). Genomic and personalized medicine: foundations and applications. Translational Research, 154(6), 277–287.PubMedCrossRef Ginsburg, G. S., & Willard, H. F. (2009). Genomic and personalized medicine: foundations and applications. Translational Research, 154(6), 277–287.PubMedCrossRef
go back to reference Giovanni, M. A., Fickie, M. R., Lehmann, L. S., Green, R. C., Meckley, L. M., Veenstra, D., et al. (2010). Health-care referrals from direct-to-consumer genetic testing. Genetic Testing and Molecular Biomarkers, 14(6), 817–819.PubMedPubMedCentralCrossRef Giovanni, M. A., Fickie, M. R., Lehmann, L. S., Green, R. C., Meckley, L. M., Veenstra, D., et al. (2010). Health-care referrals from direct-to-consumer genetic testing. Genetic Testing and Molecular Biomarkers, 14(6), 817–819.PubMedPubMedCentralCrossRef
go back to reference Green, E. D., Guyer, M. S., & National Human Genome Research Institute. (2011). Charting a course for genomic medicine from base pairs to bedside. Nature, 470(7333), 204–213.PubMedCrossRef Green, E. D., Guyer, M. S., & National Human Genome Research Institute. (2011). Charting a course for genomic medicine from base pairs to bedside. Nature, 470(7333), 204–213.PubMedCrossRef
go back to reference Guttmacher, A. E., Porteous, M. E., & McInerney, J. D. (2007). Educating health-care professionals about genetics and genomics. Nature Reviews Genetics, 8(2), 151–157.PubMedCrossRef Guttmacher, A. E., Porteous, M. E., & McInerney, J. D. (2007). Educating health-care professionals about genetics and genomics. Nature Reviews Genetics, 8(2), 151–157.PubMedCrossRef
go back to reference Kaufman, D. J., Bollinger, J. M., Dvoskin, R. L., & Scott, J. A. (2012). Risky business: risk perception and the use of medical services among customers of DTC personal genetic testing. Journal of Genetic Counseling, 21(3), 413–422.PubMedCrossRef Kaufman, D. J., Bollinger, J. M., Dvoskin, R. L., & Scott, J. A. (2012). Risky business: risk perception and the use of medical services among customers of DTC personal genetic testing. Journal of Genetic Counseling, 21(3), 413–422.PubMedCrossRef
go back to reference Khoury, M. J. (2010). Dealing with the evidence dilemma in genomics and personalized medicine. Clinical Pharmacology and Therapeutics, 87(6), 635–638.PubMedCrossRef Khoury, M. J. (2010). Dealing with the evidence dilemma in genomics and personalized medicine. Clinical Pharmacology and Therapeutics, 87(6), 635–638.PubMedCrossRef
go back to reference Klitzman, R., Chung, W., Marder, K., Shanmugham, A., Chin, L. J., Stark, M., et al. (2013). Attitudes and practices among internists concerning genetic testing. Journal of Genetic Counseling, 22(1), 90–100.PubMedCrossRef Klitzman, R., Chung, W., Marder, K., Shanmugham, A., Chin, L. J., Stark, M., et al. (2013). Attitudes and practices among internists concerning genetic testing. Journal of Genetic Counseling, 22(1), 90–100.PubMedCrossRef
go back to reference Kraja, A. T., Hunt, S. C., Rao, D. C., Dávila-Román, V. G., Arnett, D. K., & Province, M. A. (2011). Genetics of hypertension and cardiovascular disease and their interconnected pathways: lessons from large studies. Current Hypertension Reports, 13(1), 46–54.PubMedPubMedCentralCrossRef Kraja, A. T., Hunt, S. C., Rao, D. C., Dávila-Román, V. G., Arnett, D. K., & Province, M. A. (2011). Genetics of hypertension and cardiovascular disease and their interconnected pathways: lessons from large studies. Current Hypertension Reports, 13(1), 46–54.PubMedPubMedCentralCrossRef
go back to reference Lander, E. S. (2011). Initial impact of the sequencing of the human genome. Nature, 470(7333), 187–197.PubMedCrossRef Lander, E. S. (2011). Initial impact of the sequencing of the human genome. Nature, 470(7333), 187–197.PubMedCrossRef
go back to reference Marshall, E. (2011). Human genome 10th anniversary. Waiting for the revolution. Science, 331(6017), 526–529.PubMedCrossRef Marshall, E. (2011). Human genome 10th anniversary. Waiting for the revolution. Science, 331(6017), 526–529.PubMedCrossRef
go back to reference Mavaddat, N., Antoniou, A. C., Easton, D. F., & Garcia-Closas, M. (2010). Genetic susceptibility to breast cancer. Molecular Oncology, 4(3), 174–191.PubMedPubMedCentralCrossRef Mavaddat, N., Antoniou, A. C., Easton, D. F., & Garcia-Closas, M. (2010). Genetic susceptibility to breast cancer. Molecular Oncology, 4(3), 174–191.PubMedPubMedCentralCrossRef
go back to reference Metcalfe, S. A., Aitken, M., & Gaff, C. L. (2008). The importance of program evaluation: how can it be applied to diverse genetics education settings? Journal of Genetic Counseling, 17(2), 170–179.PubMedCrossRef Metcalfe, S. A., Aitken, M., & Gaff, C. L. (2008). The importance of program evaluation: how can it be applied to diverse genetics education settings? Journal of Genetic Counseling, 17(2), 170–179.PubMedCrossRef
go back to reference Nippert, I., Harris, H. J., Julian-Reynier, C., Kristoffersson, U., Ten Kate, L. P., Anionwu, E., et al. (2011). Confidence of primary care physicians in their ability to carry out basic medical genetic tasks – a European survey in five countries – Part 1. Journal of Community Genetics, 2(1), 1–11.PubMedCrossRef Nippert, I., Harris, H. J., Julian-Reynier, C., Kristoffersson, U., Ten Kate, L. P., Anionwu, E., et al. (2011). Confidence of primary care physicians in their ability to carry out basic medical genetic tasks – a European survey in five countries – Part 1. Journal of Community Genetics, 2(1), 1–11.PubMedCrossRef
go back to reference O’Daniel, J. M. (2011). The prospect of genome-guided preventative medicine: a need and opportunity for genetic counselors. Journal of Genetic Counseling, 19(4), 315–327.CrossRef O’Daniel, J. M. (2011). The prospect of genome-guided preventative medicine: a need and opportunity for genetic counselors. Journal of Genetic Counseling, 19(4), 315–327.CrossRef
go back to reference Rees, G., Young, M. A., Gaff, C., & Martin, P. R. (2006). A qualitative study of health professionals’ views regarding provision of information about health-protective behaviors during genetic consultation for breast cancer. Journal of Genetic Counseling, 15(2), 95–104.PubMedCrossRef Rees, G., Young, M. A., Gaff, C., & Martin, P. R. (2006). A qualitative study of health professionals’ views regarding provision of information about health-protective behaviors during genetic consultation for breast cancer. Journal of Genetic Counseling, 15(2), 95–104.PubMedCrossRef
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, 21(3), 402–412.PubMedCrossRef 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, 21(3), 402–412.PubMedCrossRef
go back to reference Weitzel, J. N., Blazer, K. R., Macdonald, D. J., Culver, J. O., & Offit, K. (2011). Genetics, genomics, and cancer risk assessment: State of the Art and future directions in the Era of personalized medicine. CA: A Cancer Journal for Clinicians, 61(5), 327–359. Weitzel, J. N., Blazer, K. R., Macdonald, D. J., Culver, J. O., & Offit, K. (2011). Genetics, genomics, and cancer risk assessment: State of the Art and future directions in the Era of personalized medicine. CA: A Cancer Journal for Clinicians, 61(5), 327–359.
Metadata
Title
Assessing the Integration of Genomic Medicine in Genetic Counseling Training Programs
Authors
Jessica Profato
Erynn S. Gordon
Shannan Dixon
Andrea Kwan
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/s10897-013-9677-0

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