Literature DB >> 20098329

The role of race and trust in tissue/blood donation for genetic research.

Jada Bussey-Jones1, Joanne Garrett, Gail Henderson, Mairead Moloney, Connie Blumenthal, Giselle Corbie-Smith.   

Abstract

BACKGROUND: Public willingness to donate tissue samples is critical to genetic research. Prior work has linked minority status and mistrust with less willingness to provide specimens. Some have suggested recruitment of prior research participants to address these barriers. We present data from a genetic epidemiology study with a request for blood and/or saliva specimens to (1) measure willingness to donate tissue/blood samples, (2) identify demographic, trust, and other factors associated with willingness to donate samples, and (3) measure willingness to participate in future genetic research.
METHODS: We surveyed participants in the North Carolina Colorectal Cancer Study, which included biologic sample collection from consenting participants. Participants were later asked about sample provision; trust in researchers, and future research participation.
RESULTS: African Americans were less likely to give a blood sample, when compared with whites (21% vs. 13%, P < 0.05). After controlling for "trust," this difference was no longer statistically significant (17% vs. 13%, P = 0.27). Those who had given samples were more likely to express willingness to participate in future research.
CONCLUSION: Despite prior participation in a genetic epidemiology study, factors associated with provision of tissue samples reflected many previously identified demographic factors (race and trust). Interventions to improve and demonstrate the trustworthiness of the research team and recruitment of subjects with a record of sample donation might enhance future study participation.

Entities:  

Mesh:

Year:  2010        PMID: 20098329      PMCID: PMC3114600          DOI: 10.1097/GIM.0b013e3181cd6689

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


  22 in total

1.  'Science is really needed--that's all I know': informed consent and the non-verbal practices of collecting blood for genetic research in northern Sweden.

Authors:  Klaus Hoeyer
Journal:  New Genet Soc       Date:  2003-12

2.  Research with stored biological samples: what do research participants want?

Authors:  Donna T Chen; Donald L Rosenstein; Palaniappan Muthappan; Susan G Hilsenbeck; Franklin G Miller; Ezekiel J Emanuel; David Wendler
Journal:  Arch Intern Med       Date:  2005-03-28

3.  Informed consent for genetic research on blood stored for more than a decade: a population based study.

Authors:  Birgitta Stegmayr; Kjell Asplund
Journal:  BMJ       Date:  2002-09-21

4.  Genetic research and donation of tissue samples to biobanks. What do potential sample donors in the Swedish general public think?

Authors:  Asa Kettis-Lindblad; Lena Ring; Eva Viberth; Mats G Hansson
Journal:  Eur J Public Health       Date:  2005-10-05       Impact factor: 3.367

5.  Through the community looking glass: reevaluating the ethical and policy implications of research on adolescent risk and sociopathology.

Authors:  C B Fisher; S A Wallace
Journal:  Ethics Behav       Date:  2000

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.  High rate of consent to bank biologic samples for future research: the Eastern Cooperative Oncology Group experience.

Authors:  Thomas Malone; Paul J Catalano; Peter J O'Dwyer; Bruce Giantonio
Journal:  J Natl Cancer Inst       Date:  2002-05-15       Impact factor: 13.506

8.  Barriers and strategies for sustained participation of African-American men in cohort studies.

Authors:  Cathrine Hoyo; M LaVerne Reid; Paul A Godley; Theodore Parrish; Lenora Smith; Marilie Gammon
Journal:  Ethn Dis       Date:  2003       Impact factor: 1.847

9.  Public expectations for return of results from large-cohort genetic research.

Authors:  Juli Murphy; Joan Scott; David Kaufman; Gail Geller; Lisa LeRoy; Kathy Hudson
Journal:  Am J Bioeth       Date:  2008-11       Impact factor: 11.229

10.  Mapping the human genome: an assessment of media coverage and public reaction.

Authors:  Ellen S Tambor; Barbara A Bernhardt; Joann Rodgers; Neil A Holtzman; Gail Geller
Journal:  Genet Med       Date:  2002 Jan-Feb       Impact factor: 8.822

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  65 in total

Review 1.  A systematic review of strategies that increase the recruitment and retention of African American adults in genetic and genomic studies.

Authors:  Vanessa A Johnson; Yolanda M Powell-Young; Elisa R Torres; Ida J Spruill
Journal:  ABNF J       Date:  2011

2.  Donation intentions for cancer genetics research among African Americans.

Authors:  Jasmine A McDonald; Benita Weathers; Frances K Barg; Andrea B Troxel; Judy A Shea; Deborah Bowen; Carmen E Guerra; Chanita Hughes Halbert
Journal:  Genet Test Mol Biomarkers       Date:  2012-01-06

3.  Engaging African-Americans about biobanks and the return of research results.

Authors:  Colin Me Halverson; Lainie Friedman Ross
Journal:  J Community Genet       Date:  2012-03-28

4.  Design and evaluation of a decision aid for inviting parents to participate in a fragile X newborn screening pilot study.

Authors:  Donald B Bailey; Megan A Lewis; Shelly L Harris; Tracey Grant; Carla Bann; Ellen Bishop; Myra Roche; Sonia Guarda; Leah Barnum; Cynthia Powell; Bradford L Therrell
Journal:  J Genet Couns       Date:  2012-06-27       Impact factor: 2.537

5.  Does an interactive trust-enhanced electronic consent improve patient experiences when asked to share their health records for research? A randomized trial.

Authors:  Christopher A Harle; Elizabeth H Golembiewski; Kiarash P Rahmanian; Babette Brumback; Janice L Krieger; Kenneth W Goodman; Arch G Mainous; Ray E Moseley
Journal:  J Am Med Inform Assoc       Date:  2019-07-01       Impact factor: 4.497

6.  Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research.

Authors:  Stephanie A Kraft; Mildred K Cho; Katherine Gillespie; Meghan Halley; Nina Varsava; Kelly E Ormond; Harold S Luft; Benjamin S Wilfond; Sandra Soo-Jin Lee
Journal:  Am J Bioeth       Date:  2018-04       Impact factor: 11.229

7.  Predictors of 4-year retention among African American and white community-dwelling participants in the UAB study of aging.

Authors:  Richard M Allman; Patricia Sawyer; Martha Crowther; Harry S Strothers; Timothy Turner; Mona N Fouad
Journal:  Gerontologist       Date:  2011-06

8.  Promoting public awareness and engagement in genome sciences.

Authors:  Susanne B Haga; Katie D Rosanbalm; Larry Boles; Genevieve M Tindall; Troy M Livingston; Julianne M O'Daniel
Journal:  J Genet Couns       Date:  2013-02-23       Impact factor: 2.537

9.  Understanding participation by African Americans in cancer genetics research.

Authors:  Jasmine A McDonald; Frances K Barg; Benita Weathers; Carmen E Guerra; Andrea B Troxel; Susan Domchek; Deborah Bowen; Judy A Shea; Chanita Hughes Halbert
Journal:  J Natl Med Assoc       Date:  2012 Jul-Aug       Impact factor: 1.798

10.  Barriers and Strategies Related to Qualitative Research on Genetic Ancestry Testing in Indigenous Communities.

Authors:  Jessica W Blanchard; Gloria Tallbull; Chantelle Wolpert; Jill Powell; Morris W Foster; Charmaine Royal
Journal:  J Empir Res Hum Res Ethics       Date:  2017-04-23       Impact factor: 1.742

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