Literature DB >> 21555865

Public perspectives on returning genetics and genomics research results.

J O'Daniel1, S B Haga.   

Abstract

BACKGROUND: The debate about returning research results has revealed different perspectives among researchers, participants and advisory groups with participants generally interested in obtaining their results. Given this preference, policies regarding return of individual research results may affect whether a potential subject chooses to participate in a study. Public attitudes, particularly those of African-Americans, toward this issue have been understudied.
METHODS: In 2008-2009, we convened 10 focus groups in Durham, N.C. to explore attitudes about returning research results and how different policies might influence their likelihood to participate in genetic/genomic studies. Transcripts were complimented by a short anonymous survey. Of 100 participants, 73% were female and 76% African-American with a median age of 40-49 years.
RESULTS: Although there was general interest in obtaining genetics research results, particularly individual results, discussants recognized many potential complexities. The option to obtain research results (individual or summary) was clearly valued and lack thereof was potentially a deterrent for genetic/genomic research enrollment.
CONCLUSIONS: Providing the option to learn research results may help strengthen relationships between investigators and participants and thereby serve as a positive influencing factor for minority communities. Consideration of the broader implications of returning research results is warranted. Engaging diverse publics is essential to gain a balance between the interests and burdens of participants and investigators.
Copyright © 2011 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2011        PMID: 21555865      PMCID: PMC3221258          DOI: 10.1159/000324933

Source DB:  PubMed          Journal:  Public Health Genomics        ISSN: 1662-4246            Impact factor:   2.000


  50 in total

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2.  Do patients participating in clinical trials want to know study results?

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3.  Attitudes about genetics in underserved, culturally diverse populations.

Authors:  Diana S Catz; Nancy S Green; Jonathan N Tobin; Michele A Lloyd-Puryear; Penny Kyler; Ann Umemoto; Jennifer Cernoch; Roxane Brown; Fredericka Wolman
Journal:  Community Genet       Date:  2005

4.  Disclosing individual results of clinical research: implications of respect for participants.

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5.  Issues of consent and feedback in a genetic epidemiological study of women with breast cancer.

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Journal:  J Med Ethics       Date:  2003-04       Impact factor: 2.903

6.  Public attitudes regarding the donation and storage of blood specimens for genetic research.

Authors:  S S Wang; F Fridinger; K M Sheedy; M J Khoury
Journal:  Community Genet       Date:  2001

7.  Offering to return results to research participants: attitudes and needs of principal investigators in the Children's Oncology Group.

Authors:  Conrad V Fernandez; Eric Kodish; Susan Shurin; Charles Weijer
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8.  "What are they going to do with the information?" Latino/Latina and African American perspectives on the Human Genome Project.

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Journal:  Health Educ Behav       Date:  2003-04

9.  Impact on survivors of retinoblastoma when informed of study results on risk of second cancers.

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Journal:  Med Pediatr Oncol       Date:  2003-07

10.  Consent for genetic research in a general population: the NHANES experience.

Authors:  Geraldine M McQuillan; Kathryn S Porter; Maria Agelli; Raynard Kington
Journal:  Genet Med       Date:  2003 Jan-Feb       Impact factor: 8.822

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  48 in total

1.  Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations.

Authors:  Susan M Wolf; Rebecca Branum; Barbara A Koenig; Gloria M Petersen; Susan A Berry; Laura M Beskow; Mary B Daly; Conrad V Fernandez; Robert C Green; Bonnie S LeRoy; Noralane M Lindor; P Pearl O'Rourke; Carmen Radecki Breitkopf; Mark A Rothstein; Brian Van Ness; Benjamin S Wilfond
Journal:  J Law Med Ethics       Date:  2015       Impact factor: 1.718

2.  Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age.

Authors:  K A Kaphingst; J Ivanovich; B B Biesecker; R Dresser; J Seo; L G Dressler; P J Goodfellow; M S Goodman
Journal:  Clin Genet       Date:  2015-05-05       Impact factor: 4.438

3.  Discussing molecular testing in oncology care: Comparing patient and physician information preferences.

Authors:  Ana P M Pinheiro; Rachel H Pocock; Jeffrey M Switchenko; Margie D Dixon; Walid L Shaib; Suresh S Ramalingam; Rebecca D Pentz
Journal:  Cancer       Date:  2017-01-31       Impact factor: 6.860

Review 4.  Incidental findings from clinical genome-wide sequencing: a review.

Authors:  Z Lohn; S Adam; P H Birch; J M Friedman
Journal:  J Genet Couns       Date:  2013-05-26       Impact factor: 2.537

5.  Return of individual results in epilepsy genomic research: A view from the field.

Authors:  Ruth Ottman; Catharine Freyer; Heather C Mefford; Annapurna Poduri; Daniel H Lowenstein
Journal:  Epilepsia       Date:  2018-08-10       Impact factor: 5.864

6.  Improving a Case-Control Study of Multiple Sclerosis Using Formative Research.

Authors:  Dhelia M Williamson; Laurie Wagner; Judy P Henry
Journal:  Univers J Public Health       Date:  2013

7.  In Different Voices: The Views of People with Disabilities about Return of Results from Precision Medicine Research.

Authors:  Maya Sabatello; Yuan Zhang; Ying Chen; Paul S Appelbaum
Journal:  Public Health Genomics       Date:  2020-04-15       Impact factor: 2.000

8.  Perceptions regarding genetic testing in populations at risk for nephropathy.

Authors:  Barry I Freedman; Alison J Fletcher; Vivek R Sanghani; Mitzie Spainhour; Angelina W Graham; Gregory B Russell; Jessica N Cooke Bailey; Ana S Iltis; Nancy M P King
Journal:  Am J Nephrol       Date:  2013-11-21       Impact factor: 3.754

9.  Attitudes of African Americans toward return of results from exome and whole genome sequencing.

Authors:  Joon-Ho Yu; Julia Crouch; Seema M Jamal; Holly K Tabor; Michael J Bamshad
Journal:  Am J Med Genet A       Date:  2013-05       Impact factor: 2.802

10.  'Information is information': a public perspective on incidental findings in clinical and research genome-based testing.

Authors:  S Daack-Hirsch; M Driessnack; A Hanish; V A Johnson; L L Shah; C M Simon; J K Williams
Journal:  Clin Genet       Date:  2013-05-03       Impact factor: 4.438

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