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Kidney Week

Abstract: TH-PO847

APOL1 Genotyping, Knowledge, and Attitudes among African American Patients: Building a Cohort in a Midwestern US Urban Community

Session Information

Category: Diversity and Equity in Kidney Health

  • 900 Diversity and Equity in Kidney Health

Authors

  • Lentine, Krista L., Saint Louis Univ, St. Louis, Missouri, United States
  • Philipneri, Marie D., Saint Louis Univ, St. Louis, Missouri, United States
  • Memon, Aliza Anwar, Saint Louis Univ, St. Louis, Missouri, United States
  • Edwards, John C., Saint Louis Univ, St. Louis, Missouri, United States
  • Mosman, Amy, Saint Louis Univ, St. Louis, Missouri, United States
  • Miyata, Kana, Saint Louis Univ, St. Louis, Missouri, United States
  • Abu Al Rub, Fadee, Saint Louis Univ, St. Louis, Missouri, United States
  • Carriker, Amber, Mid-America Transplant, St. Louis, Missouri, United States
  • Freedman, Barry I., Wake Forest, Winston Salem, North Carolina, United States
  • Elsurer Afsar, Rengin, Saint Louis Univ, St. Louis, Missouri, United States
  • Afsar, Baris, Saint Louis Univ, St. Louis, Missouri, United States
  • Muiru, Anthony N., UCSF, San Francisco, California, United States
  • Hsu, Chi-yuan, UCSF, San Francisco, California, United States
  • Caliskan, Yasar, Saint Louis Univ, St. Louis, Missouri, United States
Background

While some past studies assessed interest in apolipoprotein L1 (APOL1) genotyping among focus groups, few studies examine attitudes and knowledge combined with the opportunity to receive individual genotyping.

Methods

We offered APOL1 genetic testing and surveyed knowledge, attitudes and concerns related to APOL1 testing and kidney risk management among self-identified African American patients (NCT05656261) including 3 mo. follow-up (Fig 1A).

Results

Among 263 participants with genotyping results to date (Jan 2019–March 2024), 16% had high-risk genotypes (2 APOL1 RRVs) and 84% were low-risk (0/1 RRV). Median eGFR2021 was 47.7 in APOL1 low-risk vs. 42.2 ml/min/1.73 m2 in high-risk groups. 50.7% of low-risk and 54.8% of high-risk groups reported family members with kidney problems. 24% of the 2 RRV group rated their overall health as poor to very poor, vs. 10% of the 0/1 RRV group.
At baseline, 86% reported they would want APOL1 testing for their family members. However, only 9.5% accepted formal genetic counseling beyond study-related education. Participants reported a variety of behavior changes may follow genotyping information (Fig 1B). The proportion who might worry about a high-risk genotype was lower at 3 mo. (18% vs 23%). 90% agreed to future research.

Conclusion

Self-identified African American patients at a Midwestern medical center report a high family history of kidney disease and were receptive to individual APOL1 genetic testing, not only in theory, but by participating in testing. Ongoing research is needed to define the interplay of genetic and environmental factors underlying kidney risk in this population.

Funding

  • Private Foundation Support