Literature DB >> 24316767

Community perceptions of genomic research: implications for addressing health disparities.

Malika Roman Isler1, Karey Sutton, R Jean Cadigan, Giselle Corbie-Smith.   

Abstract

BACKGROUND: Increasing the engagement of racial and ethnic minorities in genomic research may help alleviate health disparities. This paper examines community perceptions of the relationships between race, genes, environment, and health disparities, and it discusses how such perceptions may influence participation in genomic research.
METHODS: We conducted semi-structured interviews with 91 African American, Latino, and white lay community members and community leaders in North Carolina. Using constant comparison methods, we identified, compared, and developed linkages between conceptual categories and respondent groups.
RESULTS: Participants described gene-environment interactions as contributing to group differences in health outcomes, expressed the belief that genetic predisposition to disease differs across groups, and said that social conditions trigger group-level genetic differences and create poorer health outcomes among African Americans. LIMITATIONS: Given the regional presence of major research institutions and the relatively high education level of many participants, this sample may not reflect the perspectives of those most disparately affected by health disparities.
CONCLUSIONS: Members from multiple community sectors share perceptions and may respond to similar approaches when attempts are made to increase participation in genomic research. Researchers may inadvertently fuel the perception that health disparities experienced by minorities are rooted in the shared genomes of a particular group as distinct from those of other groups. The way researchers use race and ethnicity in recruitment, analysis, and communication of research findings inaccurately implies that there are genetic differences between races, when categories of social experience or ancestry may more accurately characterize health differences. Understanding these issues is crucial to designing effective community engagement strategies, recruitment plans, and messages about genomic research, which could ultimately help to lessen health disparities.

Entities:  

Mesh:

Year:  2013        PMID: 24316767

Source DB:  PubMed          Journal:  N C Med J        ISSN: 0029-2559


  9 in total

1.  Inclusion of diverse populations in genomic research and health services: Genomix workshop report.

Authors:  Savio S Mathew; Julian Barwell; Nasaim Khan; Ella Lynch; Michael Parker; Nadeem Qureshi
Journal:  J Community Genet       Date:  2017-07-28

2.  From "Personalized" to "Precision" Medicine: The Ethical and Social Implications of Rhetorical Reform in Genomic Medicine.

Authors:  Eric Juengst; Michelle L McGowan; Jennifer R Fishman; Richard A Settersten
Journal:  Hastings Cent Rep       Date:  2016-09       Impact factor: 2.683

Review 3.  APOL1 Genetic Testing in Living Kidney Transplant Donors.

Authors:  Sumit Mohan; Ana S Iltis; Deirdre Sawinski; James M DuBois
Journal:  Am J Kidney Dis       Date:  2019-04-11       Impact factor: 8.860

4.  Attitudes and experiences regarding genetic research among persons of African descent.

Authors:  Denise M Scott; Veronica G Thomas; Jane Otado; Faun Rockcliffe; Omotomilade Olopoenia; Dietrich Johnson; Shawneequa Callier
Journal:  J Community Genet       Date:  2019-05-06

5.  "He Beat You in the Blood": Knowledge and Beliefs About the Transmission of Traits Among Latinos from Mexico and Central America.

Authors:  Joanne C Sandberg; Guadalupe Rodriguez; Timothy D Howard; Sara A Quandt; Thomas A Arcury
Journal:  J Immigr Minor Health       Date:  2017-02

6.  Increasing participation in genomic research and biobanking through community-based capacity building.

Authors:  Elizabeth Gross Cohn; Maryam Husamudeen; Elaine L Larson; Janet K Williams
Journal:  J Genet Couns       Date:  2014-09-18       Impact factor: 2.537

7.  Respecting Autonomy And Enabling Diversity: The Effect Of Eligibility And Enrollment On Research Data Demographics.

Authors:  Kayte Spector-Bagdady; Shengpu Tang; Sarah Jabbour; W Nicholson Price; Ana Bracic; Melissa S Creary; Sachin Kheterpal; Chad M Brummett; Jenna Wiens
Journal:  Health Aff (Millwood)       Date:  2021-12       Impact factor: 6.301

Review 8.  Current practice of public involvement activities in biomedical research and innovation: a systematic qualitative review.

Authors:  Jonas Lander; Tobias Hainz; Irene Hirschberg; Daniel Strech
Journal:  PLoS One       Date:  2014-12-03       Impact factor: 3.240

9.  Experiences and practices of key research team members in obtaining informed consent for pharmacogenetic research among people living with HIV: a qualitative study.

Authors:  Sylvia Nabukenya; Joseph Ochieng; David Kaawa-Mafigiri; Ian Munabi; Janet Nakigudde; Frederick Nelson Nakwagala; John Barugahare; Betty Kwagala; Charles Ibingira; Adelline Twimwijukye; Nelson Sewankambo; Erisa Sabakaki Mwaka
Journal:  Res Ethics       Date:  2022-02-07
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.