Literature DB >> 27735926

Experiences from a pilot program bringing BRCA1/2 genetic screening to theUS Ashkenazi Jewish population.

Chana Wiesman1,2, Esther Rose1,2, Allison Grant2, Adam Zimilover2, Susan Klugman1,2, Nicole Schreiber-Agus1,2,3.   

Abstract

PURPOSE: The notion of offering population-based screening to the Ashkenazi Jewish (AJ) population for the BRCA1/2 founder mutations continues to gain support. A program called the BRCAcommunity initiative was designed to identify the benefits and barriers associated with implementing this screening in a clinical setting.
METHODS: Interested AJ individuals were stratified into high-risk (HR) and low-risk (LR) groups based on self-reported cancer histories. Those at HR were offered traditional genetic counseling/testing; those at LR were offered group genetic counseling and subsidized AJ BRCA founder mutation testing.
RESULTS: During the pilot year, 62% of initial registrants and 53% of ultimate study participants were classified into the HR group. Among the 101 HR and 88 LR study participants, 8 and 2 BRCA carriers were identified, respectively. The LR carriers would have been missed by current mechanisms. Survey responses provided insight into the motivations and fears associated with pursuing testing, the efficacy of the initiative design, and challenges that exist on multiple levels, including the community, health-care providers, and insurance coverage.
CONCLUSION: Although the medical value of identifying presymptomatic BRCA carriers in Ashkenazi Jews is evident, further measures need to be taken before this effort can be accomplished on a large scale.Genet Med advance online publication 13 October 2016.

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Year:  2016        PMID: 27735926     DOI: 10.1038/gim.2016.154

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  8 in total

1.  Understanding Factors Associated with Uptake of BRCA1/2 Genetic Testing among Orthodox Jewish Women in the USA Using a Mixed-Methods Approach.

Authors:  Meghna S Trivedi; Hilary Colbeth; Haeseung Yi; Alejandro Vanegas; Rebecca Starck; Wendy K Chung; Paul S Appelbaum; Rita Kukafka; Isaac Schechter; Katherine D Crew
Journal:  Public Health Genomics       Date:  2019-06-04       Impact factor: 2.000

2.  Targeted BRCA1/2 population screening among Ashkenazi Jewish individuals using a web-enabled medical model: An observational cohort study.

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Journal:  Genet Med       Date:  2021-12-03       Impact factor: 8.864

Review 3.  Breast cancer in low-middle income countries: abnormality in splicing and lack of targeted treatment options.

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Journal:  Am J Cancer Res       Date:  2020-05-01       Impact factor: 5.942

Review 4.  Next-Generation Service Delivery: A Scoping Review of Patient Outcomes Associated with Alternative Models of Genetic Counseling and Genetic Testing for Hereditary Cancer.

Authors:  Jeanna M McCuaig; Susan Randall Armel; Melanie Care; Alexandra Volenik; Raymond H Kim; Kelly A Metcalfe
Journal:  Cancers (Basel)       Date:  2018-11-13       Impact factor: 6.639

5.  Characterization of BRCA1 and BRCA2 genetic variants in a cohort of Bahraini breast cancer patients using next-generation sequencing.

Authors:  Fatima Al Hannan; Michael B Keogh; Safa Taha; Latifa Al Buainain
Journal:  Mol Genet Genomic Med       Date:  2019-05-26       Impact factor: 2.183

6.  Compassion and Empathy in Basic Medical Science Teaching: A Suggested Model.

Authors:  Dana R Crawford
Journal:  Cureus       Date:  2021-12-06

7.  BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway.

Authors:  Cecilie Heramb; Teresia Wangensteen; Eli Marie Grindedal; Sarah Louise Ariansen; Sheba Lothe; Ketil Riddervold Heimdal; Lovise Mæhle
Journal:  Hered Cancer Clin Pract       Date:  2018-01-10       Impact factor: 2.857

Review 8.  From public health genomics to precision public health: a 20-year journey.

Authors:  Muin J Khoury; M Scott Bowen; Mindy Clyne; W David Dotson; Marta L Gwinn; Ridgely Fisk Green; Katherine Kolor; Juan L Rodriguez; Anja Wulf; Wei Yu
Journal:  Genet Med       Date:  2017-12-14       Impact factor: 8.822

  8 in total

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