Literature DB >> 31402353

Who's on third? Regulation of third-party genetic interpretation services.

Christi J Guerrini1, Jennifer K Wagner2, Sarah C Nelson3, Gail H Javitt4, Amy L McGuire5.   

Abstract

In recent years, third-party genetic interpretation services have emerged to help individuals understand their raw genetic data obtained from researchers, clinicians, and direct-to-consumer genetic testing companies. The objectives of these services vary but include matching users to genetic relatives, selling customized diet and fitness plans, and providing health risk assessments. As these services proliferate, concerns are being raised about their accuracy, safety, and privacy practices. Thus far, US regulatory agencies have not taken an official position with respect to third-party genetic interpretation services, which has caused uncertainty regarding whether and how they might be regulated. To clarify this area, we analyzed their potential oversight by four US agencies that generally have been active in the regulation of genetic testing services and information: the Centers for Medicare and Medicaid Services, the Food and Drug Administration, the Department of Health and Human Services' Office of Civil Rights, and the Federal Trade Commission. We conclude that the scope of federal jurisdiction over third-party genetic interpretation services-while limited-could be appropriate at this time, subject to agency clarification and appropriate exercise of oversight.

Entities:  

Keywords:  ELSI; direct-to-consumer screening and testing; genetic privacy; genetic services; health policy

Mesh:

Year:  2019        PMID: 31402353     DOI: 10.1038/s41436-019-0627-6

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


  2 in total

1.  Who Knows What, and When?: A Survey of the Privacy Policies Proffered by U.S. Direct-to-Consumer Genetic Testing Companies.

Authors:  Christopher Slobogin; James W Hazel
Journal:  Cornell J Law Public Policy       Date:  2018

2.  The Limits of FDA's Authority to Regulate Clinical Research Involving High-Throughput DNA Sequencing.

Authors:  Barbara J Evans
Journal:  Food Drug Law J       Date:  2015       Impact factor: 0.619

  2 in total
  11 in total

Review 1.  Genetic testing for hereditary gastrointestinal cancer syndromes: Interpreting results in today's practice.

Authors:  Jacquelyn M Powers; Jessica E Ebrahimzadeh; Bryson W Katona
Journal:  Curr Treat Options Gastroenterol       Date:  2019-12

2.  The Federal Trade Commission and Consumer Protections for Mobile Health Apps.

Authors:  Jennifer K Wagner
Journal:  J Law Med Ethics       Date:  2020-03       Impact factor: 1.718

3.  Core values of genomic citizen science: results from a qualitative interview study.

Authors:  Christi J Guerrini; Meredith Trejo; Isabel Canfield; Amy L McGuire
Journal:  Biosocieties       Date:  2020-09-28

4.  Direct-to-consumer genomic testing: Are nurses prepared?

Authors:  Elena Flowers; Heather Leutwyler; Janet K Shim
Journal:  Nursing       Date:  2020-08

5.  Genomic Sequencing Capacity, Data Retention, and Personal Access to Raw Data in Europe.

Authors:  Shaman Narayanasamy; Varvara Markina; Adrian Thorogood; Adriana Blazkova; Mahsa Shabani; Bartha M Knoppers; Barbara Prainsack; Robert Koesters
Journal:  Front Genet       Date:  2020-05-06       Impact factor: 4.599

6.  MySeq: privacy-protecting browser-based personal Genome analysis for genomics education and exploration.

Authors:  Michael D Linderman; Leo McElroy; Laura Chang
Journal:  BMC Med Genomics       Date:  2019-11-27       Impact factor: 3.063

7.  Parental Access to Children's Raw Genomic Data in Canada: Legal Rights and Professional Responsibility.

Authors:  Michael J S Beauvais; Adrian M Thorogood; Michael J Szego; Karine Sénécal; M'an H Zawati; Bartha Maria Knoppers
Journal:  Front Genet       Date:  2021-03-31       Impact factor: 4.599

8.  Direct-to-consumer genetic testing: Prospective users' attitudes toward information about ancestry and biological relationships.

Authors:  James W Hazel; Catherine Hammack-Aviran; Kathleen M Brelsford; Bradley A Malin; Laura M Beskow; Ellen Wright Clayton
Journal:  PLoS One       Date:  2021-11-29       Impact factor: 3.240

9.  Genomic health data generation in the UK: a 360 view.

Authors:  Elizabeth Ormondroyd; Peter Border; Judith Hayward; Andrew Papanikitas
Journal:  Eur J Hum Genet       Date:  2021-10-19       Impact factor: 5.351

Review 10.  Three decades of genetic privacy: a metaphoric journey.

Authors:  Bartha Maria Knoppers; Michael J S Beauvais
Journal:  Hum Mol Genet       Date:  2021-10-01       Impact factor: 6.150

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