Non-classical human leucocyte antigens in ankylosing spondylitis
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://doi.org/10.1136/rmdopen-2018-000677 |
Resumo: | Objectives Ankylosing spondylitis (AS) is the most prevalent form of spondyloarthritis, with a known genetic association with the HLA-B27 molecule. The aim of this study was to assess the contribution of the HLA-G, HLA-E and HLA-F to AS susceptibility/protection in Portuguese patients with HLA-B27 AS and HLA-B27 unaffected controls. Methods High-resolution typing of HLA-G, HLA - E and HLA - F was performed in 228 patients with HLA-B27 AS and 244 HLA-B27 unaffected controls. Allelic, genotypic and haplotypic frequencies were compared between cohorts. To replicate the results, single nucleotide polymorphisms (SNPs) in HLA-E and HLA-F genes were typed in Australian cohorts. For further confirmation, a group of European-descent patients with AS and unaffected controls were genotyped for Major Histocompatibility Complex SNPs using the Illumina microarray. Results In the Portuguese population, no significant differences were found in HLA-G. For HLA-E, a significant difference was detected for the genotype HLA-E∗01:01:01/01:03:01 (p=0.009; pc=0.009; OR=0.51), with a protection effect. For HLA-F, significant differences were detected in the allele HLA-F∗01:01:02 (p=0.0049; pc=0.0098; OR=0.60) and corresponding SNP rs2075682 (p=0.0004; pc=0.0008; OR=0.53), suggesting protection and in the genotype HLA-F∗01:01:01/01:03:01 (p=0.011; pc=0.043; OR=2.00), suggesting a susceptibility effect. Three G-E-F haplotypes with significant differences were detected but occur in a very small number of individuals. The only significant differences detected in the replication studies were for HLA-E rs1059510 in the Australians and for HLA-F rs1736924 in the European-descent cohorts. Conclusion Our results reveal suggestive AS protective and susceptibility effects from both HLA-E and HLA - F loci, however with population differences. To our knowledge, this is the first study showing association of HLA-F with AS. |
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Non-classical human leucocyte antigens in ankylosing spondylitisPossible association with HLA-E and HLA-Fankylosing spondylitisautoimmune diseasesgene polymorphismHLAinflammationspondyloarthritisRheumatologyImmunology and AllergyImmunologyObjectives Ankylosing spondylitis (AS) is the most prevalent form of spondyloarthritis, with a known genetic association with the HLA-B27 molecule. The aim of this study was to assess the contribution of the HLA-G, HLA-E and HLA-F to AS susceptibility/protection in Portuguese patients with HLA-B27 AS and HLA-B27 unaffected controls. Methods High-resolution typing of HLA-G, HLA - E and HLA - F was performed in 228 patients with HLA-B27 AS and 244 HLA-B27 unaffected controls. Allelic, genotypic and haplotypic frequencies were compared between cohorts. To replicate the results, single nucleotide polymorphisms (SNPs) in HLA-E and HLA-F genes were typed in Australian cohorts. For further confirmation, a group of European-descent patients with AS and unaffected controls were genotyped for Major Histocompatibility Complex SNPs using the Illumina microarray. Results In the Portuguese population, no significant differences were found in HLA-G. For HLA-E, a significant difference was detected for the genotype HLA-E∗01:01:01/01:03:01 (p=0.009; pc=0.009; OR=0.51), with a protection effect. For HLA-F, significant differences were detected in the allele HLA-F∗01:01:02 (p=0.0049; pc=0.0098; OR=0.60) and corresponding SNP rs2075682 (p=0.0004; pc=0.0008; OR=0.53), suggesting protection and in the genotype HLA-F∗01:01:01/01:03:01 (p=0.011; pc=0.043; OR=2.00), suggesting a susceptibility effect. Three G-E-F haplotypes with significant differences were detected but occur in a very small number of individuals. The only significant differences detected in the replication studies were for HLA-E rs1059510 in the Australians and for HLA-F rs1736924 in the European-descent cohorts. Conclusion Our results reveal suggestive AS protective and susceptibility effects from both HLA-E and HLA - F loci, however with population differences. To our knowledge, this is the first study showing association of HLA-F with AS.NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)Centro de Estudos de Doenças Crónicas (CEDOC)RUNSantos, Margarida RodriguesCouto, Ana RitaForoni, IrisBettencourt, Bruno FilipeLi, ZhixiuMeneses, RaquelWheeler, LawriePereira, JoaquimPimentel-Santos, FernandoFonseca, João EuricoAlves, HelenaMartinho, AntónioLima, ManuelaBrown, Matthew A.Bruges-Armas, Jácome2018-07-18T22:16:30Z2018-06-012018-06-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.1136/rmdopen-2018-000677eng2044-6055PURE: 5477315http://www.scopus.com/inward/record.url?scp=85049483719&partnerID=8YFLogxKhttps://doi.org/10.1136/rmdopen-2018-000677info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T04:22:39Zoai:run.unl.pt:10362/41963Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:31:25.710919Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Non-classical human leucocyte antigens in ankylosing spondylitis Possible association with HLA-E and HLA-F |
title |
Non-classical human leucocyte antigens in ankylosing spondylitis |
spellingShingle |
Non-classical human leucocyte antigens in ankylosing spondylitis Santos, Margarida Rodrigues ankylosing spondylitis autoimmune diseases gene polymorphism HLA inflammation spondyloarthritis Rheumatology Immunology and Allergy Immunology |
title_short |
Non-classical human leucocyte antigens in ankylosing spondylitis |
title_full |
Non-classical human leucocyte antigens in ankylosing spondylitis |
title_fullStr |
Non-classical human leucocyte antigens in ankylosing spondylitis |
title_full_unstemmed |
Non-classical human leucocyte antigens in ankylosing spondylitis |
title_sort |
Non-classical human leucocyte antigens in ankylosing spondylitis |
author |
Santos, Margarida Rodrigues |
author_facet |
Santos, Margarida Rodrigues Couto, Ana Rita Foroni, Iris Bettencourt, Bruno Filipe Li, Zhixiu Meneses, Raquel Wheeler, Lawrie Pereira, Joaquim Pimentel-Santos, Fernando Fonseca, João Eurico Alves, Helena Martinho, António Lima, Manuela Brown, Matthew A. Bruges-Armas, Jácome |
author_role |
author |
author2 |
Couto, Ana Rita Foroni, Iris Bettencourt, Bruno Filipe Li, Zhixiu Meneses, Raquel Wheeler, Lawrie Pereira, Joaquim Pimentel-Santos, Fernando Fonseca, João Eurico Alves, Helena Martinho, António Lima, Manuela Brown, Matthew A. Bruges-Armas, Jácome |
author2_role |
author author author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM) Centro de Estudos de Doenças Crónicas (CEDOC) RUN |
dc.contributor.author.fl_str_mv |
Santos, Margarida Rodrigues Couto, Ana Rita Foroni, Iris Bettencourt, Bruno Filipe Li, Zhixiu Meneses, Raquel Wheeler, Lawrie Pereira, Joaquim Pimentel-Santos, Fernando Fonseca, João Eurico Alves, Helena Martinho, António Lima, Manuela Brown, Matthew A. Bruges-Armas, Jácome |
dc.subject.por.fl_str_mv |
ankylosing spondylitis autoimmune diseases gene polymorphism HLA inflammation spondyloarthritis Rheumatology Immunology and Allergy Immunology |
topic |
ankylosing spondylitis autoimmune diseases gene polymorphism HLA inflammation spondyloarthritis Rheumatology Immunology and Allergy Immunology |
description |
Objectives Ankylosing spondylitis (AS) is the most prevalent form of spondyloarthritis, with a known genetic association with the HLA-B27 molecule. The aim of this study was to assess the contribution of the HLA-G, HLA-E and HLA-F to AS susceptibility/protection in Portuguese patients with HLA-B27 AS and HLA-B27 unaffected controls. Methods High-resolution typing of HLA-G, HLA - E and HLA - F was performed in 228 patients with HLA-B27 AS and 244 HLA-B27 unaffected controls. Allelic, genotypic and haplotypic frequencies were compared between cohorts. To replicate the results, single nucleotide polymorphisms (SNPs) in HLA-E and HLA-F genes were typed in Australian cohorts. For further confirmation, a group of European-descent patients with AS and unaffected controls were genotyped for Major Histocompatibility Complex SNPs using the Illumina microarray. Results In the Portuguese population, no significant differences were found in HLA-G. For HLA-E, a significant difference was detected for the genotype HLA-E∗01:01:01/01:03:01 (p=0.009; pc=0.009; OR=0.51), with a protection effect. For HLA-F, significant differences were detected in the allele HLA-F∗01:01:02 (p=0.0049; pc=0.0098; OR=0.60) and corresponding SNP rs2075682 (p=0.0004; pc=0.0008; OR=0.53), suggesting protection and in the genotype HLA-F∗01:01:01/01:03:01 (p=0.011; pc=0.043; OR=2.00), suggesting a susceptibility effect. Three G-E-F haplotypes with significant differences were detected but occur in a very small number of individuals. The only significant differences detected in the replication studies were for HLA-E rs1059510 in the Australians and for HLA-F rs1736924 in the European-descent cohorts. Conclusion Our results reveal suggestive AS protective and susceptibility effects from both HLA-E and HLA - F loci, however with population differences. To our knowledge, this is the first study showing association of HLA-F with AS. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-07-18T22:16:30Z 2018-06-01 2018-06-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://doi.org/10.1136/rmdopen-2018-000677 |
url |
https://doi.org/10.1136/rmdopen-2018-000677 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
2044-6055 PURE: 5477315 http://www.scopus.com/inward/record.url?scp=85049483719&partnerID=8YFLogxK https://doi.org/10.1136/rmdopen-2018-000677 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799137937409966080 |