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

Author:

Batista Liz Joao Carlos,Genre FernandaORCID,Pulito-Cueto VerónicaORCID,Remuzgo-Martínez SaraORCID,Prieto-Peña Diana,Márquez Ana,Ortego-Centeno Norberto,Leonardo María Teresa,Peñalba Ana,Narváez JavierORCID,Martín-Penagos LuisORCID,Belmar-Vega Lara,Gómez-Fernández Cristina,Miranda-Filloy José A.,Caminal-Montero LuisORCID,Collado Paz,De Árgila Diego,Quiroga-Colina Patricia,Vicente-Rabaneda Esther F.,Triguero-Martínez AnaORCID,Rubio Esteban,León Luque Manuel,Blanco-Madrigal Juan María,Galíndez-Agirregoikoa Eva,Martín JavierORCID,Gualillo OresteORCID,Blanco Ricardo,Castañeda Santos,González-Gay Miguel A.ORCID,López-Mejías RaquelORCID

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.

Funder

ISCIII and European Union FEDER

Publisher

MDPI AG

Subject

General Medicine

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