Literature DB >> 22814860

Public awareness and use of direct-to-consumer personal genomic tests from four state population-based surveys, and implications for clinical and public health practice.

Katherine Kolor1, Debra Duquette, Amy Zlot, Joan Foland, Beth Anderson, Rebecca Giles, Jennifer Wrathall, Muin J Khoury.   

Abstract

PURPOSE: Direct-to-consumer personal genomic tests are widely available, but population-based data are limited on awareness and use of these tests among the general public in the United States.
METHODS: We assessed awareness and use of direct-to-consumer personal genomic tests in Connecticut, Michigan, Oregon, and Utah using the 2009 Behavioral Risk Factor Surveillance System and compared the state results to the 2008 national HealthStyles survey results.
RESULTS: Awareness was the highest in Oregon (29.1%) and the lowest in Michigan (15.8%). Factors associated with awareness across all states and nationally were higher education, higher income, and increasing age, except among those 75 years or older. Less than 1% of respondents had used the tests, with about one-half to three-quarters of those sharing the results with a health-care provider.
CONCLUSIONS: Awareness of direct-to-consumer genetic tests is greater in this study as compared with a related study conducted in 2006, whereas use is similarly low in both studies. The few respondents who reported using the tests often reported sharing their results with their health-care provider, indicating an important opportunity for health-care providers to offer patient education regarding these tests. Public health agencies have important roles in surveillance, education, and policy development on direct-to-consumer genomic tests.

Entities:  

Mesh:

Year:  2012        PMID: 22814860      PMCID: PMC5624323          DOI: 10.1038/gim.2012.67

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  28 in total

1.  Science and regulation. Regulating direct-to-consumer personal genome testing.

Authors:  Amy L McGuire; Barbara J Evans; Timothy Caulfield; Wylie Burke
Journal:  Science       Date:  2010-10-08       Impact factor: 47.728

2.  Perception of direct-to-consumer genetic testing and direct-to-consumer advertising of genetic tests among members of a large managed care organization.

Authors:  Alanna Kulchak Rahm; Heather Spencer Feigelson; Nicole Wagner; Anh Quynh Le; Eve Halterman; Nadine Cornish; James W Dearing
Journal:  J Genet Couns       Date:  2012-01-26       Impact factor: 2.537

3.  Risky business: risk perception and the use of medical services among customers of DTC personal genetic testing.

Authors:  David J Kaufman; Juli M Bollinger; Rachel L Dvoskin; Joan A Scott
Journal:  J Genet Couns       Date:  2012-01-26       Impact factor: 2.537

4.  Public awareness and use of direct-to-consumer genetic tests: results from 3 state population-based surveys, 2006.

Authors:  Katrina A B Goddard; Debra Duquette; Amy Zlot; Jenny Johnson; Ann Annis-Emeott; Patrick W Lee; Mary Pat Bland; Karen L Edwards; Kristin Oehlke; Rebecca T Giles; Ann Rafferty; Michelle L Cook; Muin J Khoury
Journal:  Am J Public Health       Date:  2008-12-23       Impact factor: 9.308

5.  Direct-to-consumer genetic testing: reliable or risky?

Authors:  David H Spencer; Christina Lockwood; Eric Topol; James P Evans; Robert C Green; Elizabeth Mansfield; Zivana Tezak
Journal:  Clin Chem       Date:  2011-09-01       Impact factor: 8.327

Review 6.  Direct to consumer genetic testing: a systematic review of position statements, policies and recommendations.

Authors:  H Skirton; L Goldsmith; L Jackson; A O'Connor
Journal:  Clin Genet       Date:  2012-04-08       Impact factor: 4.438

7.  Genomic risk profiling: attitudes and use in personal and clinical care of primary care physicians who offer risk profiling.

Authors:  Susanne B Haga; Madeline M Carrig; Julianne M O'Daniel; Lori A Orlando; Ley A Killeya-Jones; Geoffrey S Ginsburg; Alex Cho
Journal:  J Gen Intern Med       Date:  2011-02-11       Impact factor: 5.128

8.  Community interest in predictive genetic testing for susceptibility to major depressive disorder in a large national sample.

Authors:  A Wilde; B Meiser; P B Mitchell; D Hadzi-Pavlovic; P R Schofield
Journal:  Psychol Med       Date:  2010-12-15       Impact factor: 7.723

9.  Informational content, literacy demands, and usability of websites offering health-related genetic tests directly to consumers.

Authors:  Christina R Lachance; Lori A H Erby; Beth M Ford; Vincent C Allen; Kimberly A Kaphingst
Journal:  Genet Med       Date:  2010-05       Impact factor: 8.822

10.  A survey of UK public interest in internet-based personal genome testing.

Authors:  Lynn F Cherkas; Juliette M Harris; Elana Levinson; Tim D Spector; Barbara Prainsack
Journal:  PLoS One       Date:  2010-10-19       Impact factor: 3.240

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  20 in total

1.  Moving the Needle on Action Around Evidence-Based Screening for Hereditary Conditions: Preparing State Chronic Disease Directors to Advance Precision Public Health.

Authors:  Amy Ponte; Samantha Greenberg; Karen Greendale; Laura Senier
Journal:  Public Health Rep       Date:  2019-03-21       Impact factor: 2.792

2.  Does personal genome testing drive service utilization in an adult preventive medicine clinic?

Authors:  Ny Hoang; Robin Hayeems; Jill Davies; Shuye Pu; Syed Wasim; Lea Velsher; James Aw; Sébastien Chénier; Dimitri J Stavropoulos; Riyana Babul-Hirji; Rosanna Weksberg; Cheryl Shuman
Journal:  J Community Genet       Date:  2017-04-03

3.  Attitudes about regulation among direct-to-consumer genetic testing customers.

Authors:  Juli Murphy Bollinger; Robert C Green; David Kaufman
Journal:  Genet Test Mol Biomarkers       Date:  2013-04-06

4.  Segmenting by risk perceptions: predicting young adults' genetic-belief profiles with health and opinion-leader covariates.

Authors:  Rachel A Smith; Marisa Greenberg; Roxanne L Parrott
Journal:  Health Commun       Date:  2013-10-10

5.  Direct-to-Consumer Genetic Testing and Personal Genomics Services: A Review of Recent Empirical Studies.

Authors:  J Scott Roberts; Jenny Ostergren
Journal:  Curr Genet Med Rep       Date:  2013-09

6.  Racial minority group interest in direct-to-consumer genetic testing: findings from the PGen study.

Authors:  Latrice Landry; Daiva Elena Nielsen; Deanna Alexis Carere; J Scott Roberts; Robert C Green
Journal:  J Community Genet       Date:  2017-09-04

7.  Differences in attitudes toward genetic testing among the public, patients, and health-care professionals in Korea.

Authors:  Heesang Eum; Mangyeong Lee; Junghee Yoon; Juhee Cho; Eun Sook Lee; Kui Son Choi; Sangwon Lee; So-Youn Jung; Myong Cheol Lim; Sun-Young Kong; Yoon Jung Chang
Journal:  Eur J Hum Genet       Date:  2018-06-18       Impact factor: 4.246

Review 8.  Understanding patient and provider perceptions and expectations of genomic medicine.

Authors:  Michael J Hall; Andrea D Forman; Susan V Montgomery; Kim L Rainey; Mary B Daly
Journal:  J Surg Oncol       Date:  2014-07-03       Impact factor: 3.454

9.  Public awareness of genetic nondiscrimination laws in four states and perceived importance of life insurance protections.

Authors:  Alicia A Parkman; Joan Foland; Beth Anderson; Debra Duquette; Holly Sobotka; Mary Lynn; Shelley Nottingham; William David Dotson; Katherine Kolor; Summer L Cox
Journal:  J Genet Couns       Date:  2014-09-23       Impact factor: 2.537

10.  Racial and ethnic differences in knowledge and attitudes about genetic testing in the US: Systematic review.

Authors:  Juan R Canedo; Stephania T Miller; Hector F Myers; Maureen Sanderson
Journal:  J Genet Couns       Date:  2019-01-21       Impact factor: 2.537

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