Publication:
IgA Vasculitis: Influence of CD40, BLK and BANK1 Gene Polymorphisms.

Loading...
Thumbnail Image

Date

2022-09-22

Authors

Batista Liz, Joao Carlos
Genre, Fernanda
Pulito-Cueto, Verónica
Remuzgo-Martínez, Sara
Prieto-Peña, Diana
Márquez, Ana
Ortego-Centeno, Norberto
Leonardo, María Teresa
Peñalba, Ana
Narváez, Javier

Advisors

Journal Title

Journal ISSN

Volume Title

Publisher

Metrics
Google Scholar
Export

Research Projects

Organizational Units

Journal Issue

Abstract

CD40, BLK and BANK1 genes involved in the development and signaling of B-cells are identified as susceptibility loci for numerous inflammatory diseases. Accordingly, we assessed the potential influence of CD40, BLK and BANK1 on the pathogenesis of immunoglobulin-A vasculitis (IgAV), predominantly a B-lymphocyte inflammatory condition. Three genetic variants within CD40 (rs1883832, rs1535045, rs4813003) and BLK (rs2254546, rs2736340, rs2618476) as well as two BANK1 polymorphisms (rs10516487, rs3733197), previously associated with inflammatory diseases, were genotyped in 382 Caucasian patients with IgAV and 955 sex- and ethnically matched healthy controls. No statistically significant differences were observed in the genotype and allele frequencies of CD40, BLK and BANK1 when IgAV patients and healthy controls were compared. Similar results were found when CD40, BLK and BANK1 genotypes or alleles frequencies were compared between patients with IgAV stratified according to the age at disease onset or to the presence/absence of gastrointestinal or renal manifestations. Moreover, no CD40, BLK and BANK1 haplotype differences were disclosed between patients with IgAV and healthy controls and between patients with IgAV stratified according to the clinical characteristics mentioned above. Our findings indicate that CD40, BLK and BANK1 do not contribute to the genetic background of IgAV.

Description

MeSH Terms

DeCS Terms

CIE Terms

Keywords

BANK1, BLK, CD40, Henoch–Schönlein purpura, IgA vasculitis, polymorphisms

Citation