Evaluation of 19 autoimmune disease-associated loci with rheumatoid arthritis in a Colombian population: Evidence for replication and gene-gene interaction

Objective. Recent studies have identified several common genes associated with multiple autoimmune diseases that support the hypothesis of the presence of shared or general autoimmunity genes. However, most of this work has been performed in populations of white origin. The main objectives of this s...

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Autores:
Tipo de recurso:
Fecha de publicación:
2011
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/22452
Acceso en línea:
https://doi.org/10.3899/jrheum.110199
https://repository.urosario.edu.co/handle/10336/22452
Palabra clave:
Adult
Allele
Article
Autoimmune disease
C8orf13 blk gene
Cd226 gene
Chromosome 18q
Chromosome 8p
Colombian
Controlled study
Ethnic group
Ethnicity
Female
Gene
Gene interaction
Gene locus
Gene mutation
Genetic association
Genetic variability
Genotype phenotype correlation
Human
Il2 gene
Il21 gene
Insulin dependent diabetes mellitus
Major clinical study
Male
Mmel1 gene
Multiple sclerosis
Mutational analysis
Population genetics
Priority journal
Rheumatoid arthritis
Single nucleotide polymorphism
Case-control studies
Colombia
Female
Genetic association studies
Genetic loci
Genetic predisposition to disease
Genetic variation
Genome-wide association study
Hispanic americans
Humans
Male
Gene-gene interaction
Genetic association
Latin america
Rheumatoid arthritis
genetic
rheumatoid
Arthritis
Epistasis
Rights
License
Abierto (Texto Completo)
Description
Summary:Objective. Recent studies have identified several common genes associated with multiple autoimmune diseases that support the hypothesis of the presence of shared or general autoimmunity genes. However, most of this work has been performed in populations of white origin. The main objectives of this study are to replicate the genotype-phenotype correlation between 19 such variants and rheumatoid arthritis (RA), and to evaluate gene-gene interactions between these genes in individuals from an ethnically homogenous nonwhite Colombian population. Methods. Nineteen single-nucleotide polymorphisms (SNP) from 16 genes/loci were genotyped in 353 RA cases and 368 controls. For each SNP, allelic and genotype-based association tests were applied to evaluate genotype-phenotype correlation. Permutation-based tests were used to validate the statistical significance. Gene-gene interactions were assessed by logistic regression. Results. We replicated the genetic association with rs13277113 (p = 0.0009, OR 1.46) and rs2736340 (p = 0.0001, OR 1.63) from C8orf13-BLK (8p23.1, associated with RA and systemic lupus erythematosus), and rs763361 (p = 0.03) from CD226 (18q22.3, associated with multiple sclerosis and type 1 diabetes) in the Colombian population. The population-attributable risks were estimated as 27%, 34%, and 16% for rs13277113, rs2736340, and rs763361, respectively. We also detected evidence for gene-gene interaction between SNP in MMEL1 (rs3890745) and C80rf13-BLK (rs13277113; p = 0.0002). Conclusion. Our results demonstrate that the IL2/IL21 region, C8orf13-BLK, and CD226 influence RA in Colombians, and RA shares some of the pathogenic mechanisms associated with other autoimmune diseases. The Journal of Rheumatology Copyright © 2011. All rights reserved.