Cited by 36Race, Genetics, and SocietyEthics in Clinical ResearchEthics and bioethics in healthcare

Racial Differences in Attitudes toward Personalized Medicine

Diaz, V.A., Mainous III, A.G., Gavin, J.K., Wilson, D.·2014·Public Health Genomics

Abstract

Background/Aims: Patient concerns regarding personalized medicine may limit its use. This study assesses racial differences in attitudes toward personalized medicine, evaluating variables that may influence these attitudes. Methods: A convenience sample of 190 adults (≥18 years) from an academic primary care practice was surveyed regarding awareness and acceptance of personalized medicine, plus concerns and benefits regarding its use. Logistic regressions predicting awareness, acceptance and concerns were performed, controlling for race, gender, marital status, education, children, internet use, and self-reported discrimination. Results: The sample was 35% non-Hispanic white (NHW) and 34.7% male. More NHW participants expressed acceptance of personalized medicine than non-Hispanic black (NHB) participants (94.4 vs. 81.9%, p = 0.0190). More NHBs were concerned about the use of genes without consent (57.3 vs. 20.6%, p < 0.0001), sharing genetic information without consent (65.0 vs. 35.6%, p < 0.0001), discrimination based on genes (62.4 vs. 34.3%, p = 0.0002), and lack of access due to cost (75.0 vs. 48.0%, p = 0.0002). In logistic regressions, NHBs (OR = 7.46, 95% CI = 3.04-18.32) and those self-reporting discrimination (OR = 2.87, 95% CI = 1.22-6.78) had more concerns about the misuse of genes and costs associated with personalized medicine. Conclusion: Racial differences exist in attitudes toward personalized medicine and may be influenced by self-reported discrimination. Further study to understand factors influencing the acceptance of personalized medicine could help encourage its use.

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Crossref · 10.1159/000354785

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  • Professionals and patients fear discrimination based on the results of genetic testing, particularly by insurance companies or employers.

    “In addition to possible disparities in access to PM, professionals and patients fear discrimination based on the results of genetic testing [27, 79, 92, 97], particularly by insurance companies or employers [46, 51, 54, 63, 86, 94–96, 98, 115].”

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Authors
Diaz, V. A., Mainous III, A. G., Gavin, J. K., & Wilson, D.
Affiliations
  • Medical University of South Carolina (US)
  • Claflin University (US)
Venue
Public Health Genomics
Publisher
S. Karger AG
Published
2013-09-27
Volume
17
Issue
1
Pages
1-6
ISSN
  • 1422-2795 (ISSN-L)
  • 1662-4246
  • 1662-8063
OpenAlex
W2051349161
Cited by
36
References
2
Citations by year
2026: 5 · 2025: 3 · 2024: 2 · 2023: 1 · 2022: 8 · 2021: 3 · 2020: 3 · 2019: 5 · 2017: 2 · 2015: 1 · 2014: 3
FWCI
0.88
Type
journal article
Language
en
Open access
closed
Locations
  • Public Health Genomics (publishedVersion)
  • PubMed (publishedVersion)
Funders
University of South Carolina
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Race, Genetics, and Society
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Ethics in Clinical Research
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Ethics and bioethics in healthcare
Keywords
personalized medicine, racial differences, patient attitudes, genetic discrimination, genetic privacy, genomic data sharing, access to genetic testing, cost barriers, non-Hispanic Black patients, self-reported discrimination, primary care patients
MeSH terms
Adolescent, Adult, Aged, Attitude to Health, Black or African American, Female, Health Surveys, Humans, Informed Consent, Male, Middle Aged, White People, Young Adult, Precision Medicine, Racism

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