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Is multiple sclerosis progression associated with the HLA-DR15 haplotype?
BACKGROUND: The prevalence of multiple sclerosis is associated with the major histocompatibility complex class II DR15 haplotype HLA-DRB1*15:01∼HLA-DRB5*01:01. OBJECTIVE: To assess whether multiple sclerosis progression is associated with the main susceptibility haplotype HLA-DRB1*15:01∼HLA-DRB5*01:...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902395/ https://www.ncbi.nlm.nih.gov/pubmed/31839982 http://dx.doi.org/10.1177/2055217319894615 |
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author | Stürner, Klarissa Hanja Siembab, Inessa Schön, Gerhard Stellmann, Jan-Patrick Heidari, Nika Fehse, Boris Heesen, Christoph Eiermann, Thomas H Martin, Roland Binder, Thomas MC |
author_facet | Stürner, Klarissa Hanja Siembab, Inessa Schön, Gerhard Stellmann, Jan-Patrick Heidari, Nika Fehse, Boris Heesen, Christoph Eiermann, Thomas H Martin, Roland Binder, Thomas MC |
author_sort | Stürner, Klarissa Hanja |
collection | PubMed |
description | BACKGROUND: The prevalence of multiple sclerosis is associated with the major histocompatibility complex class II DR15 haplotype HLA-DRB1*15:01∼HLA-DRB5*01:01. OBJECTIVE: To assess whether multiple sclerosis progression is associated with the main susceptibility haplotype HLA-DRB1*15:01∼HLA-DRB5*01:01. METHODS: Patients (n = 1230) and healthy controls (n = 2110) were genotyped for HLA-DRB1 and HLA-DRB5. The baseline Expanded Disability Status Scale (EDSS) score was determined and patients were followed for at least 3 years. RESULTS: After follow-up of the consecutive cohort 349 patients were classified as having clinical isolated syndrome and 881 patients as having multiple sclerosis. The susceptibility allele HLA-DRB1*15:01 was more frequent in clinical isolated syndrome (odds ratio 1.56) and multiple sclerosis (odds ratio 3.17) compared to controls. HLA- DRB1*15:01 was the only enriched HLA-DRB1 allele in multiple sclerosis patients. Comparison of clinical characteristics between HLA-DRB1*15:01∼HLA-DRB5*01:01 negative and positive patients with multiple sclerosis showed that baseline EDSS score, disease duration and frequency of the category secondary progressive multiple sclerosis with relapse were increased in the HLA-DRB1*15:01∼HLA-DRB5*01:01 positive group. CONCLUSION: The study confirmed HLA-DRB1*15:01 and HLA-DRB5*01:01 as the main susceptibility alleles and showed weak indirect evidence for a role in progression of the disease. |
format | Online Article Text |
id | pubmed-6902395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-69023952019-12-13 Is multiple sclerosis progression associated with the HLA-DR15 haplotype? Stürner, Klarissa Hanja Siembab, Inessa Schön, Gerhard Stellmann, Jan-Patrick Heidari, Nika Fehse, Boris Heesen, Christoph Eiermann, Thomas H Martin, Roland Binder, Thomas MC Mult Scler J Exp Transl Clin Original Research Paper BACKGROUND: The prevalence of multiple sclerosis is associated with the major histocompatibility complex class II DR15 haplotype HLA-DRB1*15:01∼HLA-DRB5*01:01. OBJECTIVE: To assess whether multiple sclerosis progression is associated with the main susceptibility haplotype HLA-DRB1*15:01∼HLA-DRB5*01:01. METHODS: Patients (n = 1230) and healthy controls (n = 2110) were genotyped for HLA-DRB1 and HLA-DRB5. The baseline Expanded Disability Status Scale (EDSS) score was determined and patients were followed for at least 3 years. RESULTS: After follow-up of the consecutive cohort 349 patients were classified as having clinical isolated syndrome and 881 patients as having multiple sclerosis. The susceptibility allele HLA-DRB1*15:01 was more frequent in clinical isolated syndrome (odds ratio 1.56) and multiple sclerosis (odds ratio 3.17) compared to controls. HLA- DRB1*15:01 was the only enriched HLA-DRB1 allele in multiple sclerosis patients. Comparison of clinical characteristics between HLA-DRB1*15:01∼HLA-DRB5*01:01 negative and positive patients with multiple sclerosis showed that baseline EDSS score, disease duration and frequency of the category secondary progressive multiple sclerosis with relapse were increased in the HLA-DRB1*15:01∼HLA-DRB5*01:01 positive group. CONCLUSION: The study confirmed HLA-DRB1*15:01 and HLA-DRB5*01:01 as the main susceptibility alleles and showed weak indirect evidence for a role in progression of the disease. SAGE Publications 2019-12-09 /pmc/articles/PMC6902395/ /pubmed/31839982 http://dx.doi.org/10.1177/2055217319894615 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Paper Stürner, Klarissa Hanja Siembab, Inessa Schön, Gerhard Stellmann, Jan-Patrick Heidari, Nika Fehse, Boris Heesen, Christoph Eiermann, Thomas H Martin, Roland Binder, Thomas MC Is multiple sclerosis progression associated with the HLA-DR15 haplotype? |
title | Is multiple sclerosis progression associated with the HLA-DR15 haplotype? |
title_full | Is multiple sclerosis progression associated with the HLA-DR15 haplotype? |
title_fullStr | Is multiple sclerosis progression associated with the HLA-DR15 haplotype? |
title_full_unstemmed | Is multiple sclerosis progression associated with the HLA-DR15 haplotype? |
title_short | Is multiple sclerosis progression associated with the HLA-DR15 haplotype? |
title_sort | is multiple sclerosis progression associated with the hla-dr15 haplotype? |
topic | Original Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902395/ https://www.ncbi.nlm.nih.gov/pubmed/31839982 http://dx.doi.org/10.1177/2055217319894615 |
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