Literature DB >> 30600270

Returning a Genomic Result for an Adult-Onset Condition to the Parents of a Newborn: Insights From the BabySeq Project.

Ingrid A Holm1,2, Amy McGuire3, Stacey Pereira3, Heidi Rehm4,5,6,7, Robert C Green6,8,9, Alan H Beggs10,2.   

Abstract

The return of information from genomic sequencing in children, especially in early life, brings up complex issues around parental autonomy, the child's future autonomy, the best interest standard, and the best interests of the family. These issues are particularly important in considering the return of genomic results for adult-onset-only conditions in children. The BabySeq Project is a randomized trial used to explore the medical, behavioral, and economic impacts of integrating genomic sequencing into the care of newborns who are healthy or sick. We discuss a case in which a variant in a gene for an actionable, adult-onset-only condition was detected, highlighting the ethical issues surrounding the return of such finding in a newborn to the newborn's parents.
Copyright © 2019 by the American Academy of Pediatrics.

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Year:  2019        PMID: 30600270      PMCID: PMC6433124          DOI: 10.1542/peds.2018-1099H

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  25 in total

1.  Disclosing Secondary Findings from Pediatric Sequencing to Families: Considering the "Benefit to Families".

Authors:  Benjamin S Wilfond; Conrad V Fernandez; Robert C Green
Journal:  J Law Med Ethics       Date:  2015       Impact factor: 1.718

2.  Predictive genetic testing of children and the role of the best interest standard.

Authors:  Lainie Friedman Ross
Journal:  J Law Med Ethics       Date:  2013       Impact factor: 1.718

Review 3.  Human genome sequencing in health and disease.

Authors:  Claudia Gonzaga-Jauregui; James R Lupski; Richard A Gibbs
Journal:  Annu Rev Med       Date:  2012       Impact factor: 13.739

Review 4.  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

5.  Opinion: predictive testing for Huntington disease in childhood: challenges and implications.

Authors:  M Bloch; M R Hayden
Journal:  Am J Hum Genet       Date:  1990-01       Impact factor: 11.025

6.  Point-counterpoint. Ethics and genomic incidental findings.

Authors:  Amy L McGuire; Steven Joffe; Barbara A Koenig; Barbara B Biesecker; Laurence B McCullough; Jennifer S Blumenthal-Barby; Timothy Caulfield; Sharon F Terry; Robert C Green
Journal:  Science       Date:  2013-05-16       Impact factor: 47.728

7.  Meta-analysis of BRCA1 and BRCA2 penetrance.

Authors:  Sining Chen; Giovanni Parmigiani
Journal:  J Clin Oncol       Date:  2007-04-10       Impact factor: 44.544

8.  A curated gene list for reporting results of newborn genomic sequencing.

Authors:  Ozge Ceyhan-Birsoy; Kalotina Machini; Matthew S Lebo; Tim W Yu; Pankaj B Agrawal; Richard B Parad; Ingrid A Holm; Amy McGuire; Robert C Green; Alan H Beggs; Heidi L Rehm
Journal:  Genet Med       Date:  2017-01-12       Impact factor: 8.822

Review 9.  Unlocking Mendelian disease using exome sequencing.

Authors:  Christian Gilissen; Alexander Hoischen; Han G Brunner; Joris A Veltman
Journal:  Genome Biol       Date:  2011-09-14       Impact factor: 13.583

10.  Reclassification of genetic-based risk predictions as GWAS data accumulate.

Authors:  Joel Krier; Richard Barfield; Robert C Green; Peter Kraft
Journal:  Genome Med       Date:  2016-02-17       Impact factor: 11.117

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  11 in total

Review 1.  Clinical utility of genomic sequencing.

Authors:  Matthew B Neu; Kevin M Bowling; Gregory M Cooper
Journal:  Curr Opin Pediatr       Date:  2019-12       Impact factor: 2.856

2.  Knowledge and attitudes on pharmacogenetics among pediatricians.

Authors:  Shahad Rahawi; Hetanshi Naik; Kathryn V Blake; Aniwaa Owusu Obeng; Rachel M Wasserman; Yoshinori Seki; Vicky L Funanage; Kimihiko Oishi; Stuart A Scott
Journal:  J Hum Genet       Date:  2020-01-27       Impact factor: 3.172

3.  Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing.

Authors:  Zoë P Mackay; Dmitry Dukhovny; Kathryn A Phillips; Alan H Beggs; Robert C Green; Richard B Parad; Kurt D Christensen
Journal:  Value Health       Date:  2020-03-20       Impact factor: 5.725

Review 4.  Opportunities, resources, and techniques for implementing genomics in clinical care.

Authors:  Teri A Manolio; Robb Rowley; Marc S Williams; Dan Roden; Geoffrey S Ginsburg; Carol Bult; Rex L Chisholm; Patricia A Deverka; Howard L McLeod; George A Mensah; Mary V Relling; Laura Lyman Rodriguez; Cecelia Tamburro; Eric D Green
Journal:  Lancet       Date:  2019-08-05       Impact factor: 79.321

Review 5.  How does the genomic naive public perceive whole genomic testing for health purposes? A scoping review.

Authors:  Isabella A Sherburn; Keri Finlay; Stephanie Best
Journal:  Eur J Hum Genet       Date:  2022-10-19       Impact factor: 5.351

6.  Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq.

Authors:  Lainie Friedman Ross; Ellen Wright Clayton
Journal:  Pediatrics       Date:  2019-11-12       Impact factor: 7.124

7.  Polygenic risk scores in the clinic: new perspectives needed on familiar ethical issues.

Authors:  Anna C F Lewis; Robert C Green
Journal:  Genome Med       Date:  2021-01-28       Impact factor: 11.117

8.  Pediatric reporting of genomic results study (PROGRESS): a mixed-methods, longitudinal, observational cohort study protocol to explore disclosure of actionable adult- and pediatric-onset genomic variants to minors and their parents.

Authors:  Juliann M Savatt; Jennifer K Wagner; Steven Joffe; Alanna Kulchak Rahm; Marc S Williams; Angela R Bradbury; F Daniel Davis; Julie Hergenrather; Yirui Hu; Melissa A Kelly; H Lester Kirchner; Michelle N Meyer; Jessica Mozersky; Sean M O'Dell; Josie Pervola; Andrea Seeley; Amy C Sturm; Adam H Buchanan
Journal:  BMC Pediatr       Date:  2020-05-15       Impact factor: 2.125

Review 9.  FDA oversight of NSIGHT genomic research: the need for an integrated systems approach to regulation.

Authors:  Laura V Milko; Flavia Chen; Kee Chan; Amy M Brower; Pankaj B Agrawal; Alan H Beggs; Jonathan S Berg; Steven E Brenner; Ingrid A Holm; Barbara A Koenig; Richard B Parad; Cynthia M Powell; Stephen F Kingsmore
Journal:  NPJ Genom Med       Date:  2019-12-10       Impact factor: 8.617

10.  Principles of Genomic Newborn Screening Programs: A Systematic Review.

Authors:  Lilian Downie; Jane Halliday; Sharon Lewis; David J Amor
Journal:  JAMA Netw Open       Date:  2021-07-01
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