Literature DB >> 21629297

Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?

Heidi Carmen Howard1, Denise Avard, Pascal Borry.   

Abstract

The genetic testing of minors within the direct-to-consumer (DTC) genetic testing (GT) context has been given relatively little attention. The issue of testing healthy children for diseases that would only develop in adulthood raises many important ethical, legal and social issues. As genetic testing is now available outside of the traditional health care system, often without even the intermediate of a health care professional, we surveyed 37 DTC GT companies regarding their policies for testing in children. Although the response rate is relatively low (35%, 13/37), our findings reveal that a clear majority of companies do perform genetic testing in minors. As such, companies testing for adult onset diseases are acting in contradiction of established professional guidelines, which state, among others, that, for predictive genetic testing, the availability of therapeutic or preventive measures is necessary for testing to be performed in asymptomatic minors. The community of stakeholders in children's health care and genetic testing should, therefore, decide which standards need to be upheld by DTC GT companies and ensure that these are met.

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Mesh:

Year:  2011        PMID: 21629297      PMCID: PMC3198149          DOI: 10.1038/ejhg.2011.94

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  21 in total

1.  The UK's policy on genetic testing services supplied direct to the public -- two spheres and two tiers.

Authors:  Neil A Holtzman
Journal:  Community Genet       Date:  1998

2.  Where there's a web, there's a way: commercial genetic testing and the Internet.

Authors:  Bryn Williams-Jones
Journal:  Community Genet       Date:  2003

3.  Blurring lines. The research activities of direct-to-consumer genetic testing companies raise questions about consumers as research subjects.

Authors:  Heidi C Howard; Bartha Maria Knoppers; Pascal Borry
Journal:  EMBO Rep       Date:  2010-07-16       Impact factor: 8.807

Review 4.  The current landscape for direct-to-consumer genetic testing: legal, ethical, and policy issues.

Authors:  Stuart Hogarth; Gail Javitt; David Melzer
Journal:  Annu Rev Genomics Hum Genet       Date:  2008       Impact factor: 8.929

Review 5.  Ethical and clinical practice considerations for genetic counselors related to direct-to-consumer marketing of genetic tests.

Authors:  Christopher H Wade; Benjamin S Wilfond
Journal:  Am J Med Genet C Semin Med Genet       Date:  2006-11-15       Impact factor: 3.908

Review 6.  Carrier testing in minors: a systematic review of guidelines and position papers.

Authors:  Pascal Borry; Jean-Pierre Fryns; Paul Schotsmans; Kris Dierickx
Journal:  Eur J Hum Genet       Date:  2006-02       Impact factor: 4.246

7.  Consent and internet-enabled human genomics.

Authors:  Greg Gibson; Gregory P Copenhaver
Journal:  PLoS Genet       Date:  2010-06-24       Impact factor: 5.917

8.  Health-related direct-to-consumer genetic testing: a review of companies' policies with regard to genetic testing in minors.

Authors:  Pascal Borry; Heidi C Howard; Karine Sénécal; Denise Avard
Journal:  Fam Cancer       Date:  2009-06-02       Impact factor: 2.375

9.  Points to consider: ethical, legal, and psychosocial implications of genetic testing in children and adolescents. American Society of Human Genetics Board of Directors, American College of Medical Genetics Board of Directors.

Authors: 
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025

10.  Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market.

Authors:  Pascal Borry; Martina C Cornel; Heidi C Howard
Journal:  J Community Genet       Date:  2010-10-08
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  16 in total

1.  An exploration of genetic health professionals' experience with direct-to-consumer genetic testing in their clinical practice.

Authors:  Gemma R Brett; Sylvia A Metcalfe; David J Amor; Jane L Halliday
Journal:  Eur J Hum Genet       Date:  2012-02-08       Impact factor: 4.246

Review 2.  Direct-to-consumer personalized genomic testing.

Authors:  Cinnamon S Bloss; Burcu F Darst; Eric J Topol; Nicholas J Schork
Journal:  Hum Mol Genet       Date:  2011-08-09       Impact factor: 6.150

Review 3.  The perspective from EASAC and FEAM on direct-to-consumer genetic testing for health-related purposes.

Authors:  Robin Fears; Volker ter Meulen
Journal:  Eur J Hum Genet       Date:  2012-11-21       Impact factor: 4.246

4.  Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies.

Authors:  Josephine Johnston; John D Lantos; Aaron Goldenberg; Flavia Chen; Erik Parens; Barbara A Koenig
Journal:  Hastings Cent Rep       Date:  2018-07       Impact factor: 2.683

5.  Paternity testing under the cloak of recreational genetics.

Authors:  Nathalie Moray; Katherina E Pink; Pascal Borry; Maarten Hd Larmuseau
Journal:  Eur J Hum Genet       Date:  2017-03-08       Impact factor: 4.246

Review 6.  Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.

Authors:  Jeffrey R Botkin; John W Belmont; Jonathan S Berg; Benjamin E Berkman; Yvonne Bombard; Ingrid A Holm; Howard P Levy; Kelly E Ormond; Howard M Saal; Nancy B Spinner; Benjamin S Wilfond; Joseph D McInerney
Journal:  Am J Hum Genet       Date:  2015-07-02       Impact factor: 11.025

7.  "Would you test your children without their consent?" and other sticky dilemmas in the field of cancer genetic testing.

Authors:  Karina L Brierley; Danielle C Bonadies; Anne Moyer; Ellen T Matloff
Journal:  Fam Cancer       Date:  2014-09       Impact factor: 2.375

Review 8.  A review of quality of life after predictive testing for and earlier identification of neurodegenerative diseases.

Authors:  Jane S Paulsen; Martha Nance; Ji-In Kim; Noelle E Carlozzi; Peter K Panegyres; Cheryl Erwin; Anita Goh; Elizabeth McCusker; Janet K Williams
Journal:  Prog Neurobiol       Date:  2013-09-11       Impact factor: 11.685

9.  Experience, knowledge, and opinions about childhood genetic testing in Batten disease.

Authors:  Heather R Adams; Katherine Rose; Erika F Augustine; Jennifer M Kwon; Elisabeth A deBlieck; Frederick J Marshall; Amy Vierhile; Jonathan W Mink; Martha A Nance
Journal:  Mol Genet Metab       Date:  2013-11-04       Impact factor: 4.797

10.  Health care providers and direct-to-consumer access and advertising of genetic testing in the United States.

Authors:  Melanie F Myers
Journal:  Genome Med       Date:  2011-12-28       Impact factor: 15.266

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