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Association between human leukocyte antigen (HLA) and end-stage renal disease (ESRD): a meta-analysis

OBJECTIVES: We recently studied the association between various human leukocyte antigen (HLA) alleles and end-stage renal disease (ESRD). According to our analysis, HLA-B*50 and HLA-DQA1*3 alleles were positively associated with ESRD, while B*40, DRB1*12, DRB1*13, and DQA1*6 alleles were negatively...

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Autores principales: Noureen, Naila, Zaidi, Nousheen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933765/
https://www.ncbi.nlm.nih.gov/pubmed/36815988
http://dx.doi.org/10.7717/peerj.14792
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author Noureen, Naila
Zaidi, Nousheen
author_facet Noureen, Naila
Zaidi, Nousheen
author_sort Noureen, Naila
collection PubMed
description OBJECTIVES: We recently studied the association between various human leukocyte antigen (HLA) alleles and end-stage renal disease (ESRD). According to our analysis, HLA-B*50 and HLA-DQA1*3 alleles were positively associated with ESRD, while B*40, DRB1*12, DRB1*13, and DQA1*6 alleles were negatively associated with ESRD. However, a single case-control study does not have enough statistical power to evaluate the possible impact of genetic polymorphism on any disease. Hence, the main objective of this meta-analysis is to determine the association between these abovementioned HLA alleles and ESRD. DESIGN: MEDLINE/PubMed, EMBASE, Web of Science, and Cochrane databases were searched through December 2020 for case-control studies on the associations between HLA polymorphisms and ESRD. Independent reviewers screened the texts of potentially eligible studies and assessed the risk of bias. The meta-analysis was conducted based on the checklists and guidelines based on PRISMA. RESULTS: We identified 26 case-control studies comprising 1,312 ESRD and 3,842 healthy subjects. A non-significant positive association was observed between HLA-B*50 (OR = 1.02, 95% CI [0.90, 1.24]), HLA-B*40 (OR = 1.75, 95% CI [0.98, 3.2]), HLA-DQA1*3, (OR = 1.17, 95% CI [0.74, 1.84]), DRB1*12 (OR = 1.05, 95% CI [0.94, 1.18]) alleles and ESRD. In addition, a non-significant negative association was observed between HLA-DRB1*13 (OR = 0.90, CI [0.81, 1.01]), HLA-DQB1*6 (OR = 0.79, 95% CI [0.58, 1.07]) alleles and ESRD. CONCLUSIONS: Our meta-analysis indicates no significant association between HLA-B*50, HLA-DQA1*3, B*40, DRB1*12, DRB1*13, and DQA1*6 alleles and ESRD. Further studies with larger sample sizes and adjustments for confounders are required to confirm these conclusions.
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spelling pubmed-99337652023-02-17 Association between human leukocyte antigen (HLA) and end-stage renal disease (ESRD): a meta-analysis Noureen, Naila Zaidi, Nousheen PeerJ Molecular Biology OBJECTIVES: We recently studied the association between various human leukocyte antigen (HLA) alleles and end-stage renal disease (ESRD). According to our analysis, HLA-B*50 and HLA-DQA1*3 alleles were positively associated with ESRD, while B*40, DRB1*12, DRB1*13, and DQA1*6 alleles were negatively associated with ESRD. However, a single case-control study does not have enough statistical power to evaluate the possible impact of genetic polymorphism on any disease. Hence, the main objective of this meta-analysis is to determine the association between these abovementioned HLA alleles and ESRD. DESIGN: MEDLINE/PubMed, EMBASE, Web of Science, and Cochrane databases were searched through December 2020 for case-control studies on the associations between HLA polymorphisms and ESRD. Independent reviewers screened the texts of potentially eligible studies and assessed the risk of bias. The meta-analysis was conducted based on the checklists and guidelines based on PRISMA. RESULTS: We identified 26 case-control studies comprising 1,312 ESRD and 3,842 healthy subjects. A non-significant positive association was observed between HLA-B*50 (OR = 1.02, 95% CI [0.90, 1.24]), HLA-B*40 (OR = 1.75, 95% CI [0.98, 3.2]), HLA-DQA1*3, (OR = 1.17, 95% CI [0.74, 1.84]), DRB1*12 (OR = 1.05, 95% CI [0.94, 1.18]) alleles and ESRD. In addition, a non-significant negative association was observed between HLA-DRB1*13 (OR = 0.90, CI [0.81, 1.01]), HLA-DQB1*6 (OR = 0.79, 95% CI [0.58, 1.07]) alleles and ESRD. CONCLUSIONS: Our meta-analysis indicates no significant association between HLA-B*50, HLA-DQA1*3, B*40, DRB1*12, DRB1*13, and DQA1*6 alleles and ESRD. Further studies with larger sample sizes and adjustments for confounders are required to confirm these conclusions. PeerJ Inc. 2023-02-13 /pmc/articles/PMC9933765/ /pubmed/36815988 http://dx.doi.org/10.7717/peerj.14792 Text en ©2023 Noureen and Zaidi https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Molecular Biology
Noureen, Naila
Zaidi, Nousheen
Association between human leukocyte antigen (HLA) and end-stage renal disease (ESRD): a meta-analysis
title Association between human leukocyte antigen (HLA) and end-stage renal disease (ESRD): a meta-analysis
title_full Association between human leukocyte antigen (HLA) and end-stage renal disease (ESRD): a meta-analysis
title_fullStr Association between human leukocyte antigen (HLA) and end-stage renal disease (ESRD): a meta-analysis
title_full_unstemmed Association between human leukocyte antigen (HLA) and end-stage renal disease (ESRD): a meta-analysis
title_short Association between human leukocyte antigen (HLA) and end-stage renal disease (ESRD): a meta-analysis
title_sort association between human leukocyte antigen (hla) and end-stage renal disease (esrd): a meta-analysis
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933765/
https://www.ncbi.nlm.nih.gov/pubmed/36815988
http://dx.doi.org/10.7717/peerj.14792
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