CIITA gene polymorphism (rs3087456) in systemic lupus erythematosus and rheumatoid arthritis: A population-based cohort study.
Suelen Cristina LimaIsaura Isabelle Fonseca Gomes da SilvaDenise de Queiroga NascimentoRonald Rodrigues de MouraMatheus da Silva MesquitaNadja Maria Jorge AsanoGisele Vagjel FernandesLucila Maria ValenteEliezer RushanskyMaria Helena Queiroz de Araújo MarianoRicardo Machado XavierJosé Artur Bogo ChiesSergio CrovellaPaula Sandrin-GarciaPublished in: International journal of immunogenetics (2021)
Systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) are influenced by genetic variants in immune system HLA genes. The Class II Major Histocompatibility Complex Transactivator (CIITA) is an important co-activator of the HLA transcriptional complex; the single nucleotide variant (SNV) rs3087456 localized in the gene promoter region (-168 A/G) has been reported as able to modify its transcription level. In our study, we assessed CIITA rs3087456 SNV in 1,044 Brazilians from two Brazilian regions (Northeast and South) to verify the association with susceptibility and clinical manifestations of (SLE) and (RA) using TaqMan SNP Genotyping Assays System. We observed a protection for a recessive model (GG x AA+AG) for RA susceptibility and increased risk for erosion development in AG genotype patients. No significant association was observed for SLE susceptibility; however, we observed significant increased risk for Class IV and V nephritis development in G allele and GG genotype patients. In conclusion, we showed the contribution of CIITA rs3087456 to SLE or RA clinical features and RA susceptibility in the studied populations.
Keyphrases
- disease activity
- systemic lupus erythematosus
- rheumatoid arthritis
- ankylosing spondylitis
- end stage renal disease
- genome wide
- interstitial lung disease
- newly diagnosed
- ejection fraction
- gene expression
- dna methylation
- peritoneal dialysis
- high throughput
- systemic sclerosis
- heat shock
- copy number
- genetic diversity
- autism spectrum disorder
- genome wide identification
- muscular dystrophy
- bioinformatics analysis