Literature DB >> 28749054

The Precision Medicine Nation.

Maya Sabatello, Paul S Appelbaum.   

Abstract

The United States' ambitious Precision Medicine Initiative proposes to accelerate exponentially the adoption of precision medicine, an approach to health care that tailors disease diagnosis, treatment, and prevention to individual variability in genes, environment, and lifestyle. It aims to achieve this by creating a cohort of volunteers for precision medicine research, accelerating biomedical research innovation, and adopting policies geared toward patients' empowerment. As strategies to implement the PMI are formulated, critical consideration of the initiative's ethical and sociopolitical dimensions is needed. Drawing on scholarship of nationalism and democracy, we discuss the PMI's construction of what we term "genomic citizenship"; the possible normative obligations arising therefrom; and the ethical, legal, and social challenges that will ensue. Although the PMI is a work in progress, discussion of the existing and emerging issues can facilitate the development of policies, structures, and procedures that can maximize the initiative's ability to produce equitable and socially sensitive outcomes. Our analysis can also be applied to other population-based, precision medicine research programs.
© 2017 The Hastings Center.

Entities:  

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Year:  2017        PMID: 28749054      PMCID: PMC5568692          DOI: 10.1002/hast.736

Source DB:  PubMed          Journal:  Hastings Cent Rep        ISSN: 0093-0334            Impact factor:   2.683


  55 in total

Review 1.  Protecting communities in pharmacogenetic and pharmacogenomic research.

Authors:  C Weijer; P B Miller
Journal:  Pharmacogenomics J       Date:  2004       Impact factor: 3.550

Review 2.  Discourse ethics as an ethics of responsibility: comparison and evaluation of citizen involvement in population genomics.

Authors:  Eric Racine
Journal:  J Law Med Ethics       Date:  2003       Impact factor: 1.718

3.  Guidelines for adolescent health research. A position paper of the Society for Adolescent Medicine.

Authors:  John S Santelli; Audrey Smith Rogers; Walter D Rosenfeld; Robert H DuRant; Nancy Dubler; Madlyn Morreale; Abigail English; Sheryl Lyss; Yolanda Wimberly; Anna Schissel
Journal:  J Adolesc Health       Date:  2003-11       Impact factor: 5.012

Review 4.  Genetic testing for hereditary cancers: the impact of gender on interest, uptake and ethical considerations.

Authors:  Lori d'Agincourt-Canning; Patricia Baird
Journal:  Crit Rev Oncol Hematol       Date:  2006-04-04       Impact factor: 6.312

5.  Population genomics and research ethics with socially identifable groups.

Authors:  Joan L McGregor
Journal:  J Law Med Ethics       Date:  2007       Impact factor: 1.718

6.  Educating underserved Latino communities about family health history using lay health advisors.

Authors:  K A Kaphingst; C R Lachance; A Gepp; L Hoyt D'Anna; B Rios-Ellis
Journal:  Public Health Genomics       Date:  2009-12-29       Impact factor: 2.000

7.  Proxy consent to research: the legal landscape.

Authors:  Elyn R Saks; Laura B Dunn; Jessica Wimer; Michael Gonzales; Scott Kim
Journal:  Yale J Health Policy Law Ethics       Date:  2008

8.  Genetic counselors' attitudes towards individuals with schizophrenia: desire for social distance and endorsement of stereotypes.

Authors:  Holly Feret; Laura Conway; Jehannine C Austin
Journal:  Patient Educ Couns       Date:  2010-03-07

9.  The therapeutic misconception: problems and solutions.

Authors:  Charles W Lidz; Paul S Appelbaum
Journal:  Med Care       Date:  2002-09       Impact factor: 2.983

10.  Issues concerning feedback about genetic testing and risk of depression.

Authors:  Kay Wilhelm; Bettina Meiser; Philip B Mitchell; Adam W Finch; Jennifer E Siegel; Gordon Parker; Peter R Schofield
Journal:  Br J Psychiatry       Date:  2009-05       Impact factor: 9.319

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  9 in total

1.  Should UK primary care be an early adopter of genomic medicine?

Authors:  Donna Dickenson; Imran Rafi; John Spicer; Andrew Papanikitas
Journal:  Br J Gen Pract       Date:  2019-07       Impact factor: 5.386

2.  Return of Value in the New Era of Biomedical Research-One Size Will Not Fit All.

Authors:  Dmitry Khodyakov; Alexandra Mendoza-Graf; Sandra Berry; Camille Nebeker; Elizabeth Bromley
Journal:  AJOB Empir Bioeth       Date:  2019-10-03

3.  The physician-patient relationship in the age of precision medicine.

Authors:  Gil Eyal; Maya Sabatello; Kathryn Tabb; Rachel Adams; Matthew Jones; Frank R Lichtenberg; Alondra Nelson; Kevin Ochsner; John Rowe; Deborah Stiles; Kavita Sivaramakrishnan; Kristen Underhill; Paul S Appelbaum
Journal:  Genet Med       Date:  2018-09-14       Impact factor: 8.822

4.  A roadmap for precision medicine research recruitment: empirical assessment of the public's willingness to participate.

Authors:  Kelsey Moriarty; Susan M Wolf; Patricia M Veach; Bonnie LeRoy; Ian M MacFarlane; Heather A Zierhut
Journal:  Per Med       Date:  2020-08-17       Impact factor: 2.512

5.  What's in a Name? The Politics of 'Precision Medicine'.

Authors:  Sarah Chan; Sonja Erikainen
Journal:  Am J Bioeth       Date:  2018-04       Impact factor: 11.229

Review 6.  Predictably unequal: understanding and addressing concerns that algorithmic clinical prediction may increase health disparities.

Authors:  Jessica K Paulus; David M Kent
Journal:  NPJ Digit Med       Date:  2020-07-30

7.  Contested futures: envisioning "Personalized," "Stratified," and "Precision" medicine.

Authors:  Sonja Erikainen; Sarah Chan
Journal:  New Genet Soc       Date:  2019-07-12

Review 8.  Governing Personalized Health: A Scoping Review.

Authors:  Philipp Trein; Joël Wagner
Journal:  Front Genet       Date:  2021-04-21       Impact factor: 4.599

9.  Precision Health: The Role of the Social and Behavioral Sciences in Advancing the Vision.

Authors:  Eric Hekler; Jasmin A Tiro; Christine M Hunter; Camille Nebeker
Journal:  Ann Behav Med       Date:  2020-11-01
  9 in total

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