Kane E Collins, Edmund Gilbert, Vincent Mauduit, Katherine A Benson, Elhussein A E Elhassan, Conall O'Seaghdha, Claire Hill, Amy Jayne McKnight, Alexander P Maxwell, Peter J van der Most, Martin H de Borst, Weihua Guan, Pamala A Jacobson, Ajay K Israni, Brendan J Keating, Graham M Lord, Salla Markkinen, Ilkka Helanterä, Kati Hyvärinen, Jukka Partanen, Stephen F Madden, Matthew B Lanktree, Sophie Limou, Gianpiero L Cavalleri, Peter J Conlon
{"title":"Donor and Recipient Polygenic Risk Scores Influence Kidney Transplant Function.","authors":"Kane E Collins, Edmund Gilbert, Vincent Mauduit, Katherine A Benson, Elhussein A E Elhassan, Conall O'Seaghdha, Claire Hill, Amy Jayne McKnight, Alexander P Maxwell, Peter J van der Most, Martin H de Borst, Weihua Guan, Pamala A Jacobson, Ajay K Israni, Brendan J Keating, Graham M Lord, Salla Markkinen, Ilkka Helanterä, Kati Hyvärinen, Jukka Partanen, Stephen F Madden, Matthew B Lanktree, Sophie Limou, Gianpiero L Cavalleri, Peter J Conlon","doi":"10.3389/ti.2025.14171","DOIUrl":null,"url":null,"abstract":"<p><p>Kidney transplant outcomes are influenced by donor and recipient age, sex, HLA mismatch, donor type, anti-rejection medication adherence and disease recurrence, but variability in transplant outcomes remains unexplained. We hypothesise that donor and recipient polygenic burden for traits related to kidney function may also influence graft function. We assembled a cohort of 6,060 living and deceased kidney donor-recipient pairs. We calculated polygenic risk scores (PRSs) for kidney function-related traits in both donors and recipients. We investigated the association between these PRSs and recipient eGFR at 1- and 5-year post-transplant as well as graft failure. Donor: hypertension PRS (<i>P</i> < 0.001), eGFR PRS (<i>P</i> < 0.001), and intracranial aneurysm PRS (<i>P</i> = 0.01), along with <i>recipient</i> eGFR PRS (<i>P</i> = 0.001) were associated with eGFR at 1-year post-transplantation. Clinical factors explained 25% of the variation in eGFR at 1-year and 13% at 5-year, with PRSs cumulatively adding 1% in both cases. PRSs were not associated with long-term graft survival. We demonstrate a small, but statistically significant association between donor and recipient PRSs and recipient graft function at 1- and 5-year post-transplant. This effect is, at present, unlikely to have clinical application and further research is required to improve PRS performance.</p>","PeriodicalId":23343,"journal":{"name":"Transplant International","volume":"38 ","pages":"14171"},"PeriodicalIF":2.7000,"publicationDate":"2025-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11913612/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transplant International","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/ti.2025.14171","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"SURGERY","Score":null,"Total":0}
引用次数: 0
Abstract
Kidney transplant outcomes are influenced by donor and recipient age, sex, HLA mismatch, donor type, anti-rejection medication adherence and disease recurrence, but variability in transplant outcomes remains unexplained. We hypothesise that donor and recipient polygenic burden for traits related to kidney function may also influence graft function. We assembled a cohort of 6,060 living and deceased kidney donor-recipient pairs. We calculated polygenic risk scores (PRSs) for kidney function-related traits in both donors and recipients. We investigated the association between these PRSs and recipient eGFR at 1- and 5-year post-transplant as well as graft failure. Donor: hypertension PRS (P < 0.001), eGFR PRS (P < 0.001), and intracranial aneurysm PRS (P = 0.01), along with recipient eGFR PRS (P = 0.001) were associated with eGFR at 1-year post-transplantation. Clinical factors explained 25% of the variation in eGFR at 1-year and 13% at 5-year, with PRSs cumulatively adding 1% in both cases. PRSs were not associated with long-term graft survival. We demonstrate a small, but statistically significant association between donor and recipient PRSs and recipient graft function at 1- and 5-year post-transplant. This effect is, at present, unlikely to have clinical application and further research is required to improve PRS performance.
期刊介绍:
The aim of the journal is to serve as a forum for the exchange of scientific information in the form of original and high quality papers in the field of transplantation. Clinical and experimental studies, as well as editorials, letters to the editors, and, occasionally, reviews on the biology, physiology, and immunology of transplantation of tissues and organs, are published. Publishing time for the latter is approximately six months, provided major revisions are not needed. The journal is published in yearly volumes, each volume containing twelve issues. Papers submitted to the journal are subject to peer review.