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The influence of HLA genotype on the development of metal hypersensitivity following joint replacement

BACKGROUND: Over five million joint replacements are performed across the world each year. Cobalt chrome (CoCr) components are used in most of these procedures. Some patients develop delayed-type hypersensitivity (DTH) responses to CoCr implants, resulting in tissue damage and revision surgery. DTH...

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Autores principales: Langton, David J., Bhalekar, Rohan M., Joyce, Thomas J., Rushton, Stephen P., Wainwright, Benjamin J., Nargol, Matthew E., Shyam, Nish, Lie, Benedicte A., Pabbruwe, Moreica B., Stewart, Alan J., Waller, Susan, Natu, Shonali, Ren, Renee, Hornick, Rachelle, Darlay, Rebecca, Su, Edwin P., Nargol, Antoni V. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232575/
https://www.ncbi.nlm.nih.gov/pubmed/35761834
http://dx.doi.org/10.1038/s43856-022-00137-0
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author Langton, David J.
Bhalekar, Rohan M.
Joyce, Thomas J.
Rushton, Stephen P.
Wainwright, Benjamin J.
Nargol, Matthew E.
Shyam, Nish
Lie, Benedicte A.
Pabbruwe, Moreica B.
Stewart, Alan J.
Waller, Susan
Natu, Shonali
Ren, Renee
Hornick, Rachelle
Darlay, Rebecca
Su, Edwin P.
Nargol, Antoni V. F.
author_facet Langton, David J.
Bhalekar, Rohan M.
Joyce, Thomas J.
Rushton, Stephen P.
Wainwright, Benjamin J.
Nargol, Matthew E.
Shyam, Nish
Lie, Benedicte A.
Pabbruwe, Moreica B.
Stewart, Alan J.
Waller, Susan
Natu, Shonali
Ren, Renee
Hornick, Rachelle
Darlay, Rebecca
Su, Edwin P.
Nargol, Antoni V. F.
author_sort Langton, David J.
collection PubMed
description BACKGROUND: Over five million joint replacements are performed across the world each year. Cobalt chrome (CoCr) components are used in most of these procedures. Some patients develop delayed-type hypersensitivity (DTH) responses to CoCr implants, resulting in tissue damage and revision surgery. DTH is unpredictable and genetic links have yet to be definitively established. METHODS: At a single site, we carried out an initial investigation to identify HLA alleles associated with development of DTH following metal-on-metal hip arthroplasty. We then recruited patients from other centres to train and validate an algorithm incorporating patient age, gender, HLA genotype, and blood metal concentrations to predict the development of DTH. Accuracy of the modelling was assessed using performance metrics including time-dependent receiver operator curves. RESULTS: Using next-generation sequencing, here we determine the HLA genotypes of 606 patients. 176 of these patients had experienced failure of their prostheses; the remaining 430 remain asymptomatic at a mean follow up of twelve years. We demonstrate that the development of DTH is associated with patient age, gender, the magnitude of metal exposure, and the presence of certain HLA class II alleles. We show that the predictive algorithm developed from this investigation performs to an accuracy suitable for clinical use, with weighted mean survival probability errors of 1.8% and 3.1% for pre-operative and post-operative models respectively. CONCLUSIONS: The development of DTH following joint replacement appears to be determined by the interaction between implant wear and a patient’s genotype. The algorithm described in this paper may improve implant selection and help direct patient surveillance following surgery. Further consideration should be given towards understanding patient-specific responses to different biomaterials.
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spelling pubmed-92325752022-06-26 The influence of HLA genotype on the development of metal hypersensitivity following joint replacement Langton, David J. Bhalekar, Rohan M. Joyce, Thomas J. Rushton, Stephen P. Wainwright, Benjamin J. Nargol, Matthew E. Shyam, Nish Lie, Benedicte A. Pabbruwe, Moreica B. Stewart, Alan J. Waller, Susan Natu, Shonali Ren, Renee Hornick, Rachelle Darlay, Rebecca Su, Edwin P. Nargol, Antoni V. F. Commun Med (Lond) Article BACKGROUND: Over five million joint replacements are performed across the world each year. Cobalt chrome (CoCr) components are used in most of these procedures. Some patients develop delayed-type hypersensitivity (DTH) responses to CoCr implants, resulting in tissue damage and revision surgery. DTH is unpredictable and genetic links have yet to be definitively established. METHODS: At a single site, we carried out an initial investigation to identify HLA alleles associated with development of DTH following metal-on-metal hip arthroplasty. We then recruited patients from other centres to train and validate an algorithm incorporating patient age, gender, HLA genotype, and blood metal concentrations to predict the development of DTH. Accuracy of the modelling was assessed using performance metrics including time-dependent receiver operator curves. RESULTS: Using next-generation sequencing, here we determine the HLA genotypes of 606 patients. 176 of these patients had experienced failure of their prostheses; the remaining 430 remain asymptomatic at a mean follow up of twelve years. We demonstrate that the development of DTH is associated with patient age, gender, the magnitude of metal exposure, and the presence of certain HLA class II alleles. We show that the predictive algorithm developed from this investigation performs to an accuracy suitable for clinical use, with weighted mean survival probability errors of 1.8% and 3.1% for pre-operative and post-operative models respectively. CONCLUSIONS: The development of DTH following joint replacement appears to be determined by the interaction between implant wear and a patient’s genotype. The algorithm described in this paper may improve implant selection and help direct patient surveillance following surgery. Further consideration should be given towards understanding patient-specific responses to different biomaterials. Nature Publishing Group UK 2022-06-24 /pmc/articles/PMC9232575/ /pubmed/35761834 http://dx.doi.org/10.1038/s43856-022-00137-0 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Langton, David J.
Bhalekar, Rohan M.
Joyce, Thomas J.
Rushton, Stephen P.
Wainwright, Benjamin J.
Nargol, Matthew E.
Shyam, Nish
Lie, Benedicte A.
Pabbruwe, Moreica B.
Stewart, Alan J.
Waller, Susan
Natu, Shonali
Ren, Renee
Hornick, Rachelle
Darlay, Rebecca
Su, Edwin P.
Nargol, Antoni V. F.
The influence of HLA genotype on the development of metal hypersensitivity following joint replacement
title The influence of HLA genotype on the development of metal hypersensitivity following joint replacement
title_full The influence of HLA genotype on the development of metal hypersensitivity following joint replacement
title_fullStr The influence of HLA genotype on the development of metal hypersensitivity following joint replacement
title_full_unstemmed The influence of HLA genotype on the development of metal hypersensitivity following joint replacement
title_short The influence of HLA genotype on the development of metal hypersensitivity following joint replacement
title_sort influence of hla genotype on the development of metal hypersensitivity following joint replacement
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232575/
https://www.ncbi.nlm.nih.gov/pubmed/35761834
http://dx.doi.org/10.1038/s43856-022-00137-0
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