Literature DB >> 35482015

Health equity in the implementation of genomics and precision medicine: A public health imperative.

Muin J Khoury1, Scott Bowen2, W David Dotson2, Emily Drzymalla2, Ridgely F Green2, Robert Goldstein3, Katherine Kolor2, Leandris C Liburd4, Laurence S Sperling5, Rebecca Bunnell6.   

Abstract

Recent reviews have emphasized the need for a health equity agenda in genomics research. To ensure that genomic discoveries can lead to improved health outcomes for all segments of the population, a health equity agenda needs to go beyond research studies. Advances in genomics and precision medicine have led to an increasing number of evidence-based applications that can reduce morbidity and mortality for millions of people (tier 1). Studies have shown lower implementation rates for selected diseases with tier 1 applications (familial hypercholesterolemia, Lynch syndrome, hereditary breast and ovarian cancer) among racial and ethnic minority groups, rural communities, uninsured or underinsured people, and those with lower education and income. We make the case that a public health agenda is needed to address disparities in implementation of genomics and precision medicine. Public health actions can be centered on population-specific needs and outcomes assessment, policy and evidence development, and assurance of delivery of effective and ethical interventions. Crucial public health activities also include engaging communities, building coalitions, improving genetic health literacy, and building a diverse workforce. Without concerted public health action, further advances in genomics with potentially broad applications could lead to further widening of health disparities in the next decade. Published by Elsevier Inc.

Entities:  

Keywords:  Genomics; Health equity; Precision medicine; Public health genomics

Mesh:

Year:  2022        PMID: 35482015      PMCID: PMC9378460          DOI: 10.1016/j.gim.2022.04.009

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.864


  61 in total

1.  Defining and Achieving Health Equity in Genomic Medicine.

Authors:  Sonya Jooma; Michael J Hahn; Lucia A Hindorff; Vence L Bonham
Journal:  Ethn Dis       Date:  2019-02-21       Impact factor: 1.847

2.  Precision medicine needs an equity agenda.

Authors: 
Journal:  Nat Med       Date:  2021-05       Impact factor: 53.440

3.  Health literacy in familial hypercholesterolemia: A cross-national study.

Authors:  Martin S Hagger; Sarah J Hardcastle; Miao Hu; See Kwok; Jie Lin; Hapizah M Nawawi; Jing Pang; Raul D Santos; Handrean Soran; Ta-Chen Su; Brian Tomlinson; Gerald F Watts
Journal:  Eur J Prev Cardiol       Date:  2018-03-29       Impact factor: 7.804

4.  The big reveal: Family disclosure patterns of BRCA genetic test results among young Black women with invasive breast cancer.

Authors:  Claire C Conley; Dana Ketcher; Maija Reblin; Monica L Kasting; Deborah Cragun; Jongphil Kim; Kimlin Tam Ashing; Cheryl L Knott; Chanita Hughes-Halbert; Tuya Pal; Susan T Vadaparampil
Journal:  J Genet Couns       Date:  2020-01-07       Impact factor: 2.537

Review 5.  Prioritizing genomic applications for action by level of evidence: a horizon-scanning method.

Authors:  W D Dotson; M P Douglas; K Kolor; A C Stewart; M S Bowen; M Gwinn; A Wulf; H M Anders; C Q Chang; M Clyne; T K Lam; S D Schully; M Marrone; W G Feero; M J Khoury
Journal:  Clin Pharmacol Ther       Date:  2014-02-19       Impact factor: 6.875

6.  Trends in hypercholesterolemia, treatment and control among United States adults.

Authors:  Earl S Ford; Chaoyang Li; William S Pearson; Guixiang Zhao; Ali H Mokdad
Journal:  Int J Cardiol       Date:  2008-12-10       Impact factor: 4.164

7.  Perceptions and Barriers on the Use of Proprotein Subtilisin/Kexin Type 9 Inhibitors in Heterozygous Familial Hypercholesterolemia (From a Survey of Primary Care Physicians and Cardiologists).

Authors:  Nathan D Wong; Matthew Bang; Robert C Block; Amy L H Peterson; Dean G Karalis
Journal:  Am J Cardiol       Date:  2021-06-17       Impact factor: 2.778

8.  Effect of Access to Prescribed PCSK9 Inhibitors on Cardiovascular Outcomes.

Authors:  Kelly D Myers; Niloofar Farboodi; Mkaya Mwamburi; William Howard; David Staszak; Samuel Gidding; Seth J Baum; Katherine Wilemon; Daniel J Rader
Journal:  Circ Cardiovasc Qual Outcomes       Date:  2019-07-23

9.  Addressing health disparities in cancer with genomics.

Authors:  Onyinye D Balogun; Olufunmilayo I Olopade
Journal:  Nat Rev Genet       Date:  2021-10       Impact factor: 59.581

10.  Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.

Authors:  Toni T Seppälä; Mev Dominguez-Valentin; Emma J Crosbie; Christoph Engel; Stefan Aretz; Finlay Macrae; Ingrid Winship; Gabriel Capella; Huw Thomas; Eivind Hovig; Maartje Nielsen; Rolf H Sijmons; Lucio Bertario; Bernardo Bonanni; Maria G Tibiletti; Giulia M Cavestro; Miriam Mints; Nathan Gluck; Lior Katz; Karl Heinimann; Carlos A Vaccaro; Kate Green; Fiona Lalloo; James Hill; Wolff Schmiegel; Deepak Vangala; Claudia Perne; Hans-Georg Strauß; Johanna Tecklenburg; Elke Holinski-Feder; Verena Steinke-Lange; Jukka-Pekka Mecklin; John-Paul Plazzer; Marta Pineda; Matilde Navarro; Joan B Vida; Revital Kariv; Guy Rosner; Tamara A Piñero; Walter Pavicic; Pablo Kalfayan; Sanne W Ten Broeke; Mark A Jenkins; Lone Sunde; Inge Bernstein; John Burn; Marc Greenblatt; Wouter H de Vos Tot Nederveen Cappel; Adriana Della Valle; Francisco Lopez-Koestner; Karin Alvarez; Reinhard Büttner; Heike Görgens; Monika Morak; Stefanie Holzapfel; Robert Hüneburg; Magnus von Knebel Doeberitz; Markus Loeffler; Silke Redler; Jürgen Weitz; Kirsi Pylvänäinen; Laura Renkonen-Sinisalo; Anna Lepistö; John L Hopper; Aung K Win; Noralane M Lindor; Steven Gallinger; Loïc Le Marchand; Polly A Newcomb; Jane C Figueiredo; Stephen N Thibodeau; Christina Therkildsen; Karin A W Wadt; Marian J E Mourits; Zohreh Ketabi; Oliver G Denton; Einar A Rødland; Hans Vasen; Florencia Neffa; Patricia Esperon; Douglas Tjandra; Gabriela Möslein; Erik Rokkones; Julian R Sampson; D G Evans; Pål Møller
Journal:  Eur J Cancer       Date:  2021-03-17       Impact factor: 9.162

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  1 in total

Review 1.  Addressing the routine failure to clinically identify monogenic cases of common disease.

Authors:  Michael F Murray; Muin J Khoury; Noura S Abul-Husn
Journal:  Genome Med       Date:  2022-06-07       Impact factor: 15.266

  1 in total

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