Literature DB >> 16113531

Attitudes and misconceptions about predictive genetic testing for cancer risk.

Abigail L Rose1, Nikki Peters, Judy A Shea, Katrina Armstrong.   

Abstract

OBJECTIVE: To describe awareness, knowledge, and attitudes about genetic testing for cancer risk among the general public.
RESULTS: Thirty-eight adults participated in focus groups in West Philadelphia, Pennsylvania. Participants' beliefs about what genetic testing is ranged from 'dianetics' to an accurate description of DNA analysis. Themes included misconceptions about genetic tests, the ability to gain control of one's life through genetic testing, anxiety that might be caused by testing, risk of insurance and employment discrimination, use of genetic information for racial or ethnic discrimination, concerns about medical information confidentiality and lack of informed consent.
CONCLUSIONS: Although there was some accurate understanding of what genetic testing is and how the results could be used, there also exist significant misconceptions. In many cases, misconceptions may be barriers to uptake of genetic testing. Dispelling these misconceptions is an important step in the translation of advances in human genomics into improvements in health.

Entities:  

Keywords:  Empirical Approach; Genetics and Reproduction

Mesh:

Year:  2005        PMID: 16113531     DOI: 10.1159/000086757

Source DB:  PubMed          Journal:  Community Genet        ISSN: 1422-2795


  19 in total

1.  Prenatal genetic testing: an investigation of determining factors affecting the decision-making process.

Authors:  Monica Pivetti; Giannino Melotti
Journal:  J Genet Couns       Date:  2012-04-03       Impact factor: 2.537

Review 2.  Global trends on fears and concerns of genetic discrimination: a systematic literature review.

Authors:  Annet Wauters; Ine Van Hoyweghen
Journal:  J Hum Genet       Date:  2016-01-07       Impact factor: 3.172

Review 3.  Improved understanding of genetic and genomic influences on drug disposition and action : implications for children.

Authors:  Denise Avard; Yann Joly
Journal:  Paediatr Drugs       Date:  2008       Impact factor: 3.022

Review 4.  Ethical issues of predictive genetic testing for diabetes.

Authors:  Susanne B Haga
Journal:  J Diabetes Sci Technol       Date:  2009-07-01

5.  The risks of absolute medical confidentiality.

Authors:  M A Crook
Journal:  Sci Eng Ethics       Date:  2011-05-25       Impact factor: 3.525

6.  Concerns about cancer risk and experiences with genetic testing in a diverse population of patients with breast cancer.

Authors:  Reshma Jagsi; Kent A Griffith; Allison W Kurian; Monica Morrow; Ann S Hamilton; John J Graff; Steven J Katz; Sarah T Hawley
Journal:  J Clin Oncol       Date:  2015-04-06       Impact factor: 44.544

7.  Genetic knowledge and attitudes of parents of children with congenital heart defects.

Authors:  Sara M Fitzgerald-Butt; Jennifer Klima; Kelly Kelleher; Deena Chisolm; Kim L McBride
Journal:  Am J Med Genet A       Date:  2014-09-24       Impact factor: 2.802

8.  The influence of health care policies and health care system distrust on willingness to undergo genetic testing.

Authors:  Katrina Armstrong; Mary Putt; Chanita Hughes Halbert; David Grande; Jerome Sanford Schwartz; Kaijun Liao; Noora Marcus; Mirar Bristol Demeter; Judy Shea
Journal:  Med Care       Date:  2012-05       Impact factor: 2.983

9.  Evolving perspectives on genetic discrimination in health insurance among health care providers.

Authors:  Carin R Huizenga; Katrina Lowstuter; Kimberly C Banks; Veronica I Lagos; Virginia O Vandergon; Jeffrey N Weitzel
Journal:  Fam Cancer       Date:  2010-06       Impact factor: 2.375

10.  "Is it really worth it to get tested?": primary care patients' impressions of predictive SNP testing for colon cancer.

Authors:  Kara-Grace Leventhal; William Tuong; Beth N Peshkin; Yasmin Salehizadeh; Mary B Fishman; Susan Eggly; Kevin FitzGerald; Marc D Schwartz; Kristi D Graves
Journal:  J Genet Couns       Date:  2012-08-22       Impact factor: 2.537

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