Revisiting the association between human leukocyte antigen and end-stage renal disease.
Multiple works have studied possible associations between human leukocyte antigen (HLA) alleles and end stage renal disease (ESRD) showing, however, contradictory and inconsistent results. Here, we revisit the association between ESRD and HLA antigens, comparing HLA polymorphism (at HLA-A, -B, -C, -...
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doaj-c6f053d30dc944549e514231bf6f00782021-03-03T22:05:34ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-01159e023887810.1371/journal.pone.0238878Revisiting the association between human leukocyte antigen and end-stage renal disease.Naila NoureenFarhad Ali ShahJan LisecHina UsmanMohammad KhalidRimsha MunirNousheen ZaidiMultiple works have studied possible associations between human leukocyte antigen (HLA) alleles and end stage renal disease (ESRD) showing, however, contradictory and inconsistent results. Here, we revisit the association between ESRD and HLA antigens, comparing HLA polymorphism (at HLA-A, -B, -C, -DRB1, -DQB1 and DQA1 loci) in ESRD patients (n = 497) and controls (n = 672). Our data identified several HLA alleles that displayed a significant positive or negative association with ESRD. We also determined whether heterozygosity or homozygosity of the ESRD-associated HLA alleles at different loci could modify the prevalence of the disease. Few HLA allele combinations displayed significant associations with ESRD, among which A*3_26 combination showed the highest strength of association (OR = 4.488, P≤ 0.05) with ESRD. Interestingly, the age of ESRD onset was not affected by HLA allele combinations at different loci. We also performed an extensive literature analysis to determine whether the association of HLA to ESRD can be similar across different ethnic groups. Our analysis showed that at least certain HLA alleles, HLA-A*11, HLA-DRB1*11, and HLA-DRB1*4, display a significant association with ESRD in different ethnic groups. The findings of our study will help in determining possible protective or susceptible roles of various HLA alleles in ESRD.https://doi.org/10.1371/journal.pone.0238878 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Naila Noureen Farhad Ali Shah Jan Lisec Hina Usman Mohammad Khalid Rimsha Munir Nousheen Zaidi |
spellingShingle |
Naila Noureen Farhad Ali Shah Jan Lisec Hina Usman Mohammad Khalid Rimsha Munir Nousheen Zaidi Revisiting the association between human leukocyte antigen and end-stage renal disease. PLoS ONE |
author_facet |
Naila Noureen Farhad Ali Shah Jan Lisec Hina Usman Mohammad Khalid Rimsha Munir Nousheen Zaidi |
author_sort |
Naila Noureen |
title |
Revisiting the association between human leukocyte antigen and end-stage renal disease. |
title_short |
Revisiting the association between human leukocyte antigen and end-stage renal disease. |
title_full |
Revisiting the association between human leukocyte antigen and end-stage renal disease. |
title_fullStr |
Revisiting the association between human leukocyte antigen and end-stage renal disease. |
title_full_unstemmed |
Revisiting the association between human leukocyte antigen and end-stage renal disease. |
title_sort |
revisiting the association between human leukocyte antigen and end-stage renal disease. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2020-01-01 |
description |
Multiple works have studied possible associations between human leukocyte antigen (HLA) alleles and end stage renal disease (ESRD) showing, however, contradictory and inconsistent results. Here, we revisit the association between ESRD and HLA antigens, comparing HLA polymorphism (at HLA-A, -B, -C, -DRB1, -DQB1 and DQA1 loci) in ESRD patients (n = 497) and controls (n = 672). Our data identified several HLA alleles that displayed a significant positive or negative association with ESRD. We also determined whether heterozygosity or homozygosity of the ESRD-associated HLA alleles at different loci could modify the prevalence of the disease. Few HLA allele combinations displayed significant associations with ESRD, among which A*3_26 combination showed the highest strength of association (OR = 4.488, P≤ 0.05) with ESRD. Interestingly, the age of ESRD onset was not affected by HLA allele combinations at different loci. We also performed an extensive literature analysis to determine whether the association of HLA to ESRD can be similar across different ethnic groups. Our analysis showed that at least certain HLA alleles, HLA-A*11, HLA-DRB1*11, and HLA-DRB1*4, display a significant association with ESRD in different ethnic groups. The findings of our study will help in determining possible protective or susceptible roles of various HLA alleles in ESRD. |
url |
https://doi.org/10.1371/journal.pone.0238878 |
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