Literature DB >> 30611438

Reconciling Opportunistic and Population Screening in Clinical Genomics.

Kyle B Brothers1, Jason L Vassy2, Robert C Green3.   

Abstract

Opportunistic genomic screening is becoming increasingly common as laboratories adopt recommendations to report secondary genomic findings. In parallel, interest in using genome sequencing as a population screening test has grown rapidly. We consider here 3 potential applications of genome sequencing for preventive medicine: (1) provider-ordered predispositional testing in healthy adults, (2) indication-based testing with opportunistic screening of secondary results, and (3) population screening in the public health context. We conclude that despite superficial similarities, there are important and fundamental differences in the way medical risks and benefits can be addressed in these 3 contexts. Recommendations to report secondary genomic findings should not be interpreted as an endorsement of population genomic screening. Ongoing work is developing the evidence that will be needed to fully justify current and future initiatives in population genomic screening. Ongoing work is developing the evidence that will be needed to fully justify current and future initiatives in population genomic screening.
Copyright © 2018 Mayo Foundation for Medical Education and Research. All rights reserved.

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Year:  2019        PMID: 30611438      PMCID: PMC6339566          DOI: 10.1016/j.mayocp.2018.08.028

Source DB:  PubMed          Journal:  Mayo Clin Proc        ISSN: 0025-6196            Impact factor:   7.616


  29 in total

1.  Look before you leap: genomic screening in obstetrics and gynecology.

Authors:  Michael C Adams; Jonathan S Berg; Mark D Pearlman; Neeta L Vora
Journal:  Obstet Gynecol       Date:  2015-06       Impact factor: 7.661

2.  Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Authors:  Robert C Green; Katrina A B Goddard; Gail P Jarvik; Laura M Amendola; Paul S Appelbaum; Jonathan S Berg; Barbara A Bernhardt; Leslie G Biesecker; Sawona Biswas; Carrie L Blout; Kevin M Bowling; Kyle B Brothers; Wylie Burke; Charlisse F Caga-Anan; Arul M Chinnaiyan; Wendy K Chung; Ellen W Clayton; Gregory M Cooper; Kelly East; James P Evans; Stephanie M Fullerton; Levi A Garraway; Jeremy R Garrett; Stacy W Gray; Gail E Henderson; Lucia A Hindorff; Ingrid A Holm; Michelle Huckaby Lewis; Carolyn M Hutter; Pasi A Janne; Steven Joffe; David Kaufman; Bartha M Knoppers; Barbara A Koenig; Ian D Krantz; Teri A Manolio; Laurence McCullough; Jean McEwen; Amy McGuire; Donna Muzny; Richard M Myers; Deborah A Nickerson; Jeffrey Ou; Donald W Parsons; Gloria M Petersen; Sharon E Plon; Heidi L Rehm; J Scott Roberts; Dan Robinson; Joseph S Salama; Sarah Scollon; Richard R Sharp; Brian Shirts; Nancy B Spinner; Holly K Tabor; Peter Tarczy-Hornoch; David L Veenstra; Nikhil Wagle; Karen Weck; Benjamin S Wilfond; Kirk Wilhelmsen; Susan M Wolf; Julia Wynn; Joon-Ho Yu
Journal:  Am J Hum Genet       Date:  2016-07-07       Impact factor: 11.025

3.  Comprehension and Data-Sharing Behavior of Direct-To-Consumer Genetic Test Customers.

Authors:  Scott P McGrath; Jason Coleman; Lotfollah Najjar; Ann Fruhling; Dhundy R Bastola
Journal:  Public Health Genomics       Date:  2016-03-08       Impact factor: 2.000

4.  The impact of personal genomics on risk perceptions and medical decision-making.

Authors:  Joshua L Krieger; Fiona Murray; J Scott Roberts; Robert C Green
Journal:  Nat Biotechnol       Date:  2016-09-08       Impact factor: 54.908

Review 5.  Human Genome Sequencing at the Population Scale: A Primer on High-Throughput DNA Sequencing and Analysis.

Authors:  Rachel L Goldfeder; Dennis P Wall; Muin J Khoury; John P A Ioannidis; Euan A Ashley
Journal:  Am J Epidemiol       Date:  2017-10-15       Impact factor: 4.897

6.  Aggregate penetrance of genomic variants for actionable disorders in European and African Americans.

Authors:  Pradeep Natarajan; Nina B Gold; Alexander G Bick; Heather McLaughlin; Peter Kraft; Heidi L Rehm; Gina M Peloso; James G Wilson; Adolfo Correa; Jonathan G Seidman; Christine E Seidman; Sekar Kathiresan; Robert C Green
Journal:  Sci Transl Med       Date:  2016-11-09       Impact factor: 17.956

7.  Points to consider in the clinical application of genomic sequencing.

Authors: 
Journal:  Genet Med       Date:  2012-08       Impact factor: 8.822

8.  Communication challenges for nongeneticist physicians relaying clinical genomic results.

Authors:  Nonie S Arora; J Kelly Davis; Christine Kirby; Amy L McGuire; Robert C Green; J S Blumenthal-Barby; Peter A Ubel
Journal:  Per Med       Date:  2017-09-15       Impact factor: 2.512

9.  ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.

Authors: 
Journal:  Genet Med       Date:  2014-11-13       Impact factor: 8.822

10.  A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health.

Authors:  Muin J Khoury; W Gregory Feero; David A Chambers; Lawrence C Brody; Nazneen Aziz; Robert C Green; A Cecile J W Janssens; Michael F Murray; Laura Lyman Rodriguez; Joni L Rutter; Sheri D Schully; Deborah M Winn; George A Mensah
Journal:  PLoS Med       Date:  2018-08-02       Impact factor: 11.069

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  10 in total

Review 1.  Management of Secondary Genomic Findings.

Authors:  Alexander E Katz; Robert L Nussbaum; Benjamin D Solomon; Heidi L Rehm; Marc S Williams; Leslie G Biesecker
Journal:  Am J Hum Genet       Date:  2020-07-02       Impact factor: 11.025

2.  Where is genetic medicine headed? Exploring the perspectives of Canadian genetic professionals on future trends using the Delphi method.

Authors:  Kennedy Borle; Nicola Kopac; Nick Dragojlovic; Elisabet Rodriguez Llorian; Jan M Friedman; Alison M Elliott; Larry D Lynd
Journal:  Eur J Hum Genet       Date:  2022-01-15       Impact factor: 5.351

3.  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

4.  Comprehension and personal value of negative non-diagnostic genetic panel testing.

Authors:  Christin Hoell; Sharon Aufox; Nora Nashawaty; Melanie F Myers; Maureen E Smith
Journal:  J Genet Couns       Date:  2020-09-18       Impact factor: 2.537

5.  Personalized medicine, digital technology and trust: a Kantian account.

Authors:  Bjørn K Myskja; Kristin S Steinsbekk
Journal:  Med Health Care Philos       Date:  2020-09-04

6.  Precision Population Medicine in Primary Care: The Sanford Chip Experience.

Authors:  Kurt D Christensen; Megan Bell; Carrie L B Zawatsky; Lauren N Galbraith; Robert C Green; Allison M Hutchinson; Leila Jamal; Jessica L LeBlanc; Jennifer R Leonhard; Michelle Moore; Lisa Mullineaux; Natasha Petry; Dylan M Platt; Sherin Shaaban; April Schultz; Bethany D Tucker; Joel Van Heukelom; Elizabeth Wheeler; Emilie S Zoltick; Catherine Hajek
Journal:  Front Genet       Date:  2021-03-12       Impact factor: 4.599

7.  Family history assessment significantly enhances delivery of precision medicine in the genomics era.

Authors:  Yasmin Bylstra; Weng Khong Lim; Sylvia Kam; Koei Wan Tham; R Ryanne Wu; Jing Xian Teo; Sonia Davila; Jyn Ling Kuan; Sock Hoai Chan; Nicolas Bertin; Cheng Xi Yang; Steve Rozen; Bin Tean Teh; Khung Keong Yeo; Stuart Alexander Cook; Saumya Shekhar Jamuar; Geoffrey S Ginsburg; Lori A Orlando; Patrick Tan
Journal:  Genome Med       Date:  2021-01-07       Impact factor: 11.117

8.  Parental Guidance Suggested: Engaging Parents as Partners in Research Studies of Genomic Screening for a Pediatric Population.

Authors:  Sabrina N Powell; Grace Byfield; Ashley Bennetone; Annabelle M Frantz; Langston K Harrison; Erin R James-Crook; Heather Osborne; Thomas H Owens; Jonathan L Shaw; Julianne O'Daniel; Laura V Milko
Journal:  Front Genet       Date:  2022-03-25       Impact factor: 4.772

9.  Opportunistic genomic screening. Recommendations of the European Society of Human Genetics.

Authors:  Guido de Wert; Wybo Dondorp; Angus Clarke; Elisabeth M C Dequeker; Christophe Cordier; Zandra Deans; Carla G van El; Florence Fellmann; Ros Hastings; Sabine Hentze; Heidi Howard; Milan Macek; Alvaro Mendes; Chris Patch; Emmanuelle Rial-Sebbag; Vigdis Stefansdottir; Martina C Cornel; Francesca Forzano
Journal:  Eur J Hum Genet       Date:  2020-11-22       Impact factor: 4.246

10.  Characteristics and experiences of patients from a community-based and consumer-directed hereditary cancer population screening initiative.

Authors:  Veronica Greve; Katherine Odom; Susanna Pudner; Neil E Lamb; Sara J Cooper; Kelly East
Journal:  HGG Adv       Date:  2021-08-24
  10 in total

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