Abstract
Rationale & Objective: African American live kidney donors (“donors”) have a greater risk for kidney failure than European American donors. Apolipoprotein L1 gene (APOL1) variants in African Americans may be associated with this disparity. Study Design: Cross-sectional mixed-methods design. Setting & Participants: African American donors at 1 transplantation center. Analytical Approach: Semistructured interviews assessed attitudes about APOL1 genetic testing, willingness to undergo APOL1 testing, hypothetical decisions about donating with 2 APOL1 variants, and demographics. Surveys assessed perceptions of ethnic identity and genetics knowledge. Interview transcriptions were analyzed using thematic analysis. Survey data were analyzed using descriptive statistics. Results: 23 donors participated in semistructured interviews. Most (96%) reported that transplantation centers should routinely offer APOL1 genetic testing to all African American potential donors. Most (87%) would have been willing to undergo APOL1 testing before donating. Although study participants noted that APOL1 testing may deter African American potential donors from donating, most (61%) would have donated even if they had 2 high-risk APOL1 variants. Several themes emerged. Study participants believed that APOL1 testing was beneficial for providing information to help donors make informed donation decisions. Participants expressed concern about APOL1 variants placing donors at harm for kidney failure, and therefore valued taking preventive health measures. Participants believed that potential donors would experience psychological distress from learning that they have 2 gene variants and could harm their recipients. Participants were apprehensive about insurance coverage and costs of APOL1 testing and feared that APOL1 genetic test results could discriminate against African Americans. Limitations: Findings may not be generalizable to African American potential donors. Conclusions: Findings suggest that African American donors support APOL1 genetic testing yet fear that APOL1 variants and genetic testing could adversely affect donors’ health and ethnic identity. Transplantation centers using APOL1 genetic testing should address African American donors’ concerns about APOL1 genetic testing to optimize future donors’ informed consent practices.
Original language | English (US) |
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Pages (from-to) | 819-833 |
Number of pages | 15 |
Journal | American Journal of Kidney Diseases |
Volume | 72 |
Issue number | 6 |
DOIs | |
State | Published - Dec 2018 |
Funding
Support: This publication was supported by the National Institute of Allergy and Infectious Diseases (grant 1 R03 AI126090-01 to Dr Gordon). Research Electronic Data Capture (REDCap), a secure online data capture application, is supported at the Feinberg School of Medicine by the Northwestern University Clinical and Translational Science Institute. Research reported in this publication was supported in part by the NIH's National Center for Advancing Translational Sciences , grant UL1TR001422 . This work was also supported in part by the Northwestern Medicine Enterprise Data Warehouse. The funders had no role in study design; collection, analysis, and interpretation of data; writing the report; and the decision to submit the report for publication. Support: This publication was supported by the National Institute of Allergy and Infectious Diseases (grant 1 R03 AI126090-01 to Dr Gordon). Research Electronic Data Capture (REDCap), a secure online data capture application, is supported at the Feinberg School of Medicine by the Northwestern University Clinical and Translational Science Institute. Research reported in this publication was supported in part by the NIH's National Center for Advancing Translational Sciences, grant UL1TR001422. This work was also supported in part by the Northwestern Medicine Enterprise Data Warehouse. The funders had no role in study design; collection, analysis, and interpretation of data; writing the report; and the decision to submit the report for publication.
Keywords
- African American
- apolipoprotein L1 (APOL1)
- cultural identity
- ethics
- ethnicity
- genetic testing
- health disparities
- informed consent
- kidney transplantation
- living donation
- medical decision making
- qualitative research
- sociocultural
ASJC Scopus subject areas
- Nephrology