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HLA-DRB1 allele distribution in Chilean population: insights into rheumatoid arthritis susceptibility and protection
Indexado
WoS WOS:001495083600001
Scopus SCOPUS_ID:105006852562
DOI 10.3389/FIMMU.2025.1594723
Año 2025
Tipo artículo de investigación

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



Introduction Rheumatoid arthritis (RA) is an autoimmune disease influenced by genetic factors, particularly HLA-DRB1 alleles. The objective of this study was to characterize the distribution of HLA-DRB1 alleles in Chilean RA patients and healthy controls (HC) and evaluate associations with susceptibility or protection, autoantibody seropositivity, and disease activity.Methods We genotyped 367 RA patients and 623 HC for HLA-DRB1 using PCR-SSO. Then, we examined allele frequencies and distribution, including known RA risk alleles of the "Shared Epitope" (SE) of HLA-DRB1 and protective (PR) alleles, using the Chi-square or Fisher's exact tests. Odds ratios with 95% confidence intervals were calculated to measure the degree of association, and unpaired T-tests were used to compare continuous variables.Results The most frequent SE alleles among RA patients were *04:01 (16.1%), *04:04 (13.9%), and *14:02 (11.7%). SE alleles *04:01, *04:04, *04:05, *04:08, and *10:01, along with non-SE alleles *09:01 and *15:02, were associated with RA susceptibility. In addition, allele *14:02 showed an association with the presence of anti-cyclic citrullinated peptides (anti-CCP) antibodies. Meanwhile, PR alleles *11:01 (14.8%) and *16:02 (9.8%) were observed most frequently in HC and RA patients, respectively. PR alleles *11:01, *11:04, and *13:01, as well as the non-PR alleles *15:01, *04:07, *03:01, *07:01, and *08:02, were associated with protection from RA, and showed no significant associations with autoantibody seropositivity.Discussion This study provides a comprehensive overview of HLA-DRB1 allele distribution in the Chilean population, identifying both well-known and novel allele associations with RA susceptibility, protection, and disease activity.

Revista



Revista ISSN
Frontiers In Immunology 1664-3224

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Disciplinas de Investigación



WOS
Immunology
Scopus
Sin Disciplinas
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



Ord. Autor Género Institución - País
1 Catalan, Diego - Universidad de Chile - Chile
2 SOTO-SAEZ, LILIAN ANDREA Mujer Universidad de Chile - Chile
Hospital Clínico Universidad de Chile - Chile
3 Neira, Oscar - Universidad de Chile - Chile
4 Cuellar-Gutierrez, Maria C. - Universidad de Chile - Chile
5 Diaz, Roberto Hombre Universidad Autónoma de Chile - Chile
Univ Santiago de Compostela USC - España
Universidade de Santiago de Compostela - España
6 Aravena, Octavio - Universidad de Chile - Chile
7 Palou, Eduard - HOSP CLIN BARCELONA - España
Hospital Clínic de Barcelona - España
8 Carrascal, Montserrat - Spanish Natl Res Council - España
Institut d'Investigacions Biomèdiques August Pi i Sunyer - IDIBAPS - España
9 Aguillon, Juan C. - Universidad de Chile - Chile
10 Maggi, Jaxaira - Spanish Natl Res Council - España
Institut d'Investigacions Biomèdiques August Pi i Sunyer - IDIBAPS - España

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Financiamiento



Fuente
Fondo Nacional de Desarrollo Científico y Tecnológico
Agencia Nacional de Investigacion y Desarrollo (ANID), Chile
Agencia Nacional de Investigación y Desarrollo
ANID-PFCHA/National Doctoral Scholarship 2018/Nz.ousco

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Agradecimientos



Agradecimiento
The author(s) declare that financial support was received for the research and/or publication of this article. This work was supported by following projects: Fondef-IDeA ID15I10080, ID15I20080, ID18I10243, REDES 180028, Fondecyt 1181853, Fondecyt 1221611, Fondecyt 1220540 and Fondecyt 1240060, all granted by Agencia Nacional de Investigacion y Desarrollo (ANID), Chile. Doctoral training of JM was supported by ANID-PFCHA/National Doctoral Scholarship 2018/N & z.ousco;21181538.
The author(s) declare that financial support was received for the research and/or publication of this article. This work was supported by following projects: Fondef-IDeA ID15I10080, ID15I20080, ID18I10243, REDES 180028, Fondecyt 1181853, Fondecyt 1221611, Fondecyt 1220540 and Fondecyt 1240060, all granted by Agencia Nacional de Investigaci\u00F3n y Desarrollo (ANID), Chile. Doctoral training of JM was supported by ANID-PFCHA/National Doctoral Scholarship 2018/N&z.ousco;21181538.

Muestra la fuente de financiamiento declarada en la publicación.