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. 2017 Jul;8(3):229-238.
doi: 10.1007/s12687-017-0308-6. Epub 2017 Jun 16.

Self-reported race and ethnicity of US biobank participants compared to the US Census

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Self-reported race and ethnicity of US biobank participants compared to the US Census

Elizabeth Gross Cohn et al. J Community Genet. 2017 Jul.

Abstract

Precision medicine envisions a future of effective diagnosis, treatment, and prevention grounded in precise understandings of the genetic and environmental determinants of disease. Given that the original genome-wide association studies represented a predominately European White population, and that diversity in genomic studies must account for genetic variation both within and across racial categories, new research studies are at a heightened risk for inadequate representation. Currently biological samples are being made available for sequencing in biobanks across the USA, but the diversity of those samples is unknown. The aims of this study were to describe the types of recruitment and enrollment materials used by US biobanks and the diversity of the samples contained within their collection. Biobank websites and brochures were evaluated for reading level, health literacy, and factors known to encourage the recruitment of minorities, such as showing pictures of diverse populations. Biobank managers were surveyed by mail on the methods and materials used for enrollment, recruitment, consent, and the self-reported race/ethnicity of biobank participants. From 51 US biobanks (68% response rate), recruitment and enrollment materials were in English only, and most of the websites and brochures exceeded a fifth-grade reading level. When compared to the 2015 US Census, self-reported race/ethnicity of participants was not significantly different for Whites (61%) and blacks (13%). The percentages were significantly lower for Hispanics and Latinos (18 vs. 7%, p = 0.00) and Hawaiian/Pacific Islanders (0.2 vs. 0.01%; p = 0.01) and higher for Asians (13 vs. 5%, p = 0.01). Materials for recruitment predominantly in English may limit participation by underrepresented populations.

Keywords: Biobanks; Health equity; Minority; Population health.

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Conflict of interest statement

Conflict of interest

The authors declare that they have no conflict of interest.

Figures

Fig. 1
Fig. 1
Website for Partners HealthCare Biobank, a repository of consented patient samples and data at Partners HealthCare System (parent organization of Massachusetts General Hospital and Brigham and Women’s Hospital). Reproduced with permission
Fig. 2
Fig. 2
Search strategy for biobanks

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