Enrollment and biospecimen collection in a multiethnic family cohort: the Northern California site of the Breast Cancer Family Registry
Autor: | Jocelyn Koo, Alice S. Whittemore, Meera Sangaramoorthy, Dee W. West, Esther M. John |
---|---|
Rok vydání: | 2019 |
Předmět: |
Adult
Cancer Research medicine.medical_specialty Adolescent Ethnic group Breast Neoplasms California White People Article Young Adult 03 medical and health sciences 0302 clinical medicine Breast cancer Risk Factors Epidemiology Humans Medicine Registries 030212 general & internal medicine Family history Risk factor Asian business.industry Public health Racial Groups Hispanic or Latino Middle Aged medicine.disease Health equity Black or African American Oncology 030220 oncology & carcinogenesis Cohort Female business Demography |
Zdroj: | Cancer Causes & Control. 30:395-408 |
ISSN: | 1573-7225 0957-5243 |
DOI: | 10.1007/s10552-019-01154-6 |
Popis: | PURPOSE: Racial/ethnic minorities are often assumed to be less willing to participate in and provide biospecimens for biomedical research. We examined racial/ethnic differences in enrollment of women with breast cancer (probands) and their first-degree relatives in the Northern California site of the Breast Cancer Family Registry from 1996-2011. METHODS: We evaluated participation in several study components, including biospecimen collection, for probands and relatives by race/ethnicity, cancer history, and other factors. RESULTS: Of 4,780 eligible probands, 76% enrolled in the family registry by completing the family history and risk factor questionnaires and 68% also provided a blood or mouthwash sample. Enrollment was highest (81%) for non-Hispanic whites (NHWs) and intermediate (73%-76%) for Hispanics, African Americans, and all Asian American subgroups, except Filipina women (66%). Of 4,279 eligible relatives, 77% enrolled in the family registry, and 65% also provided a biospecimen sample. Enrollment was highest for NHWs (87%) and lowest for Chinese (68%) and Filipinas (67%). Among those enrolled, biospecimen collection rates were similar for NHW, Hispanic, and African American women, both for probands (92%-95%) and relatives (82%-87%), but lower for some Asian-American subgroups (probands: 72%-88%; relatives: 71%-88%), foreign-born Asian Americans, and probands those who were more recent immigrants or had low English language proficiency. CONCLUSIONS: These results show that racial/ethnic minority populations are willing to provide biospecimen samples for research, although some Asian American subgroups in particular may need more directed recruitment methods. To address long-standing and well-documented cancer health disparities, minority populations need equal opportunities to contribute to biomedical research. |
Databáze: | OpenAIRE |
Externí odkaz: |