Literature DB >> 33715055

The promise of public health ethics for precision medicine: the case of newborn preventive genomic sequencing.

Ainsley J Newson1.   

Abstract

Precision medicine aims to tailor medical treatment to match individual characteristics and to stratify individuals to concentrate benefits and avoid harm. It has recently been joined by precision public health-the application of precision medicine at population scale to decrease morbidity and optimise population health. Newborn preventive genomic sequencing (NPGS) provides a helpful case study to consider how we should approach ethical questions in precision public health. In this paper, I use NPGS as a case in point to argue that both precision medicine and precision public health need public health ethics. I make this argument in two parts. First, I claim that discussions of ethics in precision medicine and NPGS tend to focus on predominantly individualistic concepts from medical ethics such as autonomy and empowerment. This highlights some deficiencies, including overlooking that choice is subject to constraints and that an individual's place in the world might impact their capacity to 'be responsible'. Second, I make the case for using a public health ethics approach when considering ethics and NPGS, and thus precision public health more broadly. I discuss how precision public health needs to be construed as a collective enterprise and not just as an aggregation of individual interests. I also show how analysing collective values and interests through concepts such as solidarity can enrich ethical discussion of NPGS and highlight previously overlooked issues. With this approach, bioethics can contribute to more just and more appropriate applications of precision medicine and precision public health, including NPGS.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.

Entities:  

Year:  2021        PMID: 33715055     DOI: 10.1007/s00439-021-02269-0

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  51 in total

1.  Public Health in the Precision-Medicine Era.

Authors:  Ronald Bayer; Sandro Galea
Journal:  N Engl J Med       Date:  2015-08-06       Impact factor: 91.245

Review 2.  Empowerment in healthcare policy making: three domains of substantive controversy.

Authors:  Luca Chiapperino; Per-Anders Tengland
Journal:  Health Promot J Austr       Date:  2015-12

3.  Revisiting Wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years.

Authors:  Anne Andermann; Ingeborg Blancquaert; Sylvie Beauchamp; Véronique Déry
Journal:  Bull World Health Organ       Date:  2008-04       Impact factor: 9.408

4.  The expansion of newborn screening: is reproductive benefit an appropriate pursuit?

Authors:  Yvonne Bombard; Fiona A Miller; Robin Z Hayeems; Denise Avard; Bartha M Knoppers; Martina C Cornel; Pascal Borry
Journal:  Nat Rev Genet       Date:  2009-10       Impact factor: 53.242

5.  Making Sense of the Genome Remains a Work in Progress.

Authors:  Wylie Burke
Journal:  JAMA       Date:  2018-09-25       Impact factor: 56.272

6.  Personal utility in genomic testing: is there such a thing?

Authors:  Eline M Bunnik; A Cecile J W Janssens; Maartje H N Schermer
Journal:  J Med Ethics       Date:  2014-05-28       Impact factor: 2.903

7.  Whole Genome Sequencing and Newborn Screening.

Authors:  Jeffrey R Botkin; Erin Rothwell
Journal:  Curr Genet Med Rep       Date:  2016-02-01

8.  Screening in the dark: ethical considerations of providing screening tests to individuals when evidence is insufficient to support screening populations.

Authors:  Ingrid M Burger; Nancy E Kass
Journal:  Am J Bioeth       Date:  2009-04       Impact factor: 11.229

9.  The role of exome sequencing in newborn screening for inborn errors of metabolism.

Authors:  Jennifer M Puck; Steven E Brenner; Aashish N Adhikari; Renata C Gallagher; Yaqiong Wang; Robert J Currier; George Amatuni; Laia Bassaganyas; Flavia Chen; Kunal Kundu; Mark Kvale; Sean D Mooney; Robert L Nussbaum; Savanna S Randi; Jeremy Sanford; Joseph T Shieh; Rajgopal Srinivasan; Uma Sunderam; Hao Tang; Dedeepya Vaka; Yangyun Zou; Barbara A Koenig; Pui-Yan Kwok; Neil Risch
Journal:  Nat Med       Date:  2020-08-10       Impact factor: 53.440

10.  The promise and peril of genomic screening in the general population.

Authors:  Michael C Adams; James P Evans; Gail E Henderson; Jonathan S Berg
Journal:  Genet Med       Date:  2015-11-05       Impact factor: 8.822

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  2 in total

1.  The case for screening in early life for 'non-treatable' disorders: ethics, evidence and proportionality. A report from the Health Council of the Netherlands.

Authors:  Shona Kalkman; Wybo Dondorp
Journal:  Eur J Hum Genet       Date:  2022-02-07       Impact factor: 5.351

2.  Newborn Screening by Genomic Sequencing: Opportunities and Challenges.

Authors:  David Bick; Arzoo Ahmed; Dasha Deen; Alessandra Ferlini; Nicolas Garnier; Dalia Kasperaviciute; Mathilde Leblond; Amanda Pichini; Augusto Rendon; Aditi Satija; Alice Tuff-Lacey; Richard H Scott
Journal:  Int J Neonatal Screen       Date:  2022-07-15
  2 in total

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