Maximizing matching, equity and survival in kidney transplantation using molecular HLA immunogenicity quantitation.

African Americans equality Allocation Graft survival HLA Kidney matching Kidney transplantation Unsupervised survival analysis

Journal

Computers in biology and medicine
ISSN: 1879-0534
Titre abrégé: Comput Biol Med
Pays: United States
ID NLM: 1250250

Informations de publication

Date de publication:
09 Apr 2024
Historique:
received: 06 12 2023
revised: 11 03 2024
accepted: 07 04 2024
medline: 20 4 2024
pubmed: 20 4 2024
entrez: 19 4 2024
Statut: aheadofprint

Résumé

HLA matching improves long-term outcomes of kidney transplantation, yet implementation challenges persist, particularly within the African American (Black) patient demographic due to donor scarcity. Consequently, kidney survival rates among Black patients significantly lag behind those of other racial groups. A refined matching scheme holds promise for improving kidney survival, with prioritized matching for Black patients potentially bolstering rates of HLA-matched transplants. To facilitate quantity, quality and equity in kidney transplants, we propose two matching algorithms based on quantification of HLA immunogenicity using the hydrophobic mismatch score (HMS) for prospective transplants. We mined the national transplant patient database (SRTR) for a diverse group of donors and recipients with known racial backgrounds. Additionally, we use novel methods to infer survival assessment in the simulated transplants generated by our matching algorithms, in the absence of actual target outcomes, utilizing modified unsupervised clustering techniques. Our allocation algorithms demonstrated the ability to match 87.7% of Black and 86.1% of White recipients under the HLA immunogenicity threshold of 10. Notably, at the lowest HMS threshold of 0, 4.4% of Black and 12.1% of White recipients were matched, a marked increase from the 1.8% and 6.6% matched under the prevailing allocation scheme. Furthermore, our allocation algorithms yielded similar or improved survival rates, as illustrated by Kaplan-Meier (KM) curves, and enhanced survival prediction accuracy, evidenced by C-indices and Integrated Brier Scores.

Identifiants

pubmed: 38640635
pii: S0010-4825(24)00536-5
doi: 10.1016/j.compbiomed.2024.108452
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

108452

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest Authors have no conflicts of interest to disclose.

Auteurs

Fayeq Jeelani Syed (FJ)

Electrical Engineering and Computer Science Department, University of Toledo, 2801 W Bancroft St., Toledo, 43606, OH, USA.

Dulat Bekbolsynov (D)

Department of Medical Microbiology and Immunology, University of Toledo Medical Center, 3000 Arlington Ave., Toledo, 43614, OH, USA.

Stanislaw Stepkowski (S)

Department of Medical Microbiology and Immunology, University of Toledo Medical Center, 3000 Arlington Ave., Toledo, 43614, OH, USA.

Devinder Kaur (D)

Electrical Engineering and Computer Science Department, University of Toledo, 2801 W Bancroft St., Toledo, 43606, OH, USA.

Robert C Green (RC)

Department of Computer Science, Bowling Green State University, 1001 E Wooster St., Bowling Green, 43403, OH, USA. Electronic address: greenr@bgsu.edu.

Classifications MeSH