Association of Recipient APOL1 Kidney Risk Alleles With Kidney Transplant Outcomes

Author:

Roy Neil12,Morales-Alvarez M. Catalina12,Anis Karim H.12,Goral Simin3,Doria Cataldo4,Kopp Jeffrey B.5,Winkler Cheryl A.6,Feng Rui7,Rosas Sylvia E.12

Affiliation:

1. Kidney and Hypertension Unit, Joslin Diabetes Center, Boston, MA.

2. Nephrology Department, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.

3. Division of Renal, Electrolyte, and Hypertension, Department of Medicine, University of Pennsylvania, Philadelphia, PA.

4. Capital Health Cancer Center, Pennington, NJ.

5. Kidney Diseases Branch, National Institute of Diabetes and Digestive and Kidney, National Institutes of Health, Bethesda, MD.

6. Cancer Innovation Laboratory, Center for Cancer Research, National Cancer Institute and the Basic Research Program, Frederick National Laboratory, Frederick, MD.

7. Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.

Abstract

Background. Kidney transplant survival in African American recipients is lower compared with non–African American transplant recipients. APOL1 risk alleles (RA) have been postulated as likely contributors. We examined the graft outcomes in kidney transplant recipients (KTRs) stratified by APOL1 RA status in a multicenter observational prospective study. Methods. The Renal Transplant Outcome Study recruited a cohort of incident KTRs at 3 transplant centers in the Philadelphia area from 1999–2004. KTRs were genotyped for APOL1 RA. Allograft and patient survival rates were compared by the presence and number of APOL1 RA. Results. Among 221 participants, approximately 43% carried 2 APOL1 RA. Recipients carrying 2 APOL1 RA demonstrated lower graft survival compared with recipients with only 1 or none of APOL1 RA at 1 y posttransplant, independently of other donor and recipient characteristics (adjusted hazard ratio 3.2 [95% confidence interval, 1.0-10.4], P = 0.05). There was no significant difference in overall survival or graft survival after 3 y posttransplantation. There was no difference in death by APOL1-risk status (P = 0.11). Conclusions. Recipients with 2 APOL1 high-risk alleles exhibited lower graft survival 1 y posttransplantation compared with recipients with only 1 or 0 APOL1 RA. Further research is required to study the combined role of the recipient and donor APOL1 genotypes in kidney transplantation.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Transplantation

Reference23 articles.

1. Racial/ethnic disparity in kidney transplantation outcomes: influence of donor and recipient characteristics.;Feyssa;J Natl Med Assoc,2009

2. Improving access to HLA-matched kidney transplants for African American patients.;Bekbolsynov;Front Immunol,2022

3. Racial disparities in renal transplant outcomes.;Isaacs;Am J Kidney Dis,1999

4. Delayed graft function: risk factors and implications for renal allograft survival.;Ojo;Transplantation,1997

5. Effect of donor factors on early graft survival in adult cadaveric renal transplantation.;Swanson;Am J Transplant,2002

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