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

Authors :
European Commission
Instituto de Salud Carlos III
Xunta de Galicia
Batista-Liz, Joao Carlos
Genre, Fernanda
Pulito-Cueto, Verónica
Remuzgo-Martínez, Sara
Prieto-Peña, Diana
Márquez, Ana
Ortego-Centeno, N.
Leonardo, María Teresa
Peñalba, Ana
Narváez, Javier
Martín-Penagos, Luis
Belmar, Lara
Gómez Fernández, Cristina
Miranda-Filloy, J. A.
Caminal-Montero, Luis
Collado, Paz
Árgila, Diego de
Quiroga, Patricia
Vicente, Esther
Triguero-Martínez, Ana
Rubio, Esteban
León Luque, Manuel
Blanco-Madrigal, Juan María
Galíndez-Agirregoikoa, E.
Martín, Javier
Gualillo, Oreste
Blanco, Ricardo
Castañeda, Santos
González-Gay, M. A.
López-Mejías, Raquel
European Commission
Instituto de Salud Carlos III
Xunta de Galicia
Batista-Liz, Joao Carlos
Genre, Fernanda
Pulito-Cueto, Verónica
Remuzgo-Martínez, Sara
Prieto-Peña, Diana
Márquez, Ana
Ortego-Centeno, N.
Leonardo, María Teresa
Peñalba, Ana
Narváez, Javier
Martín-Penagos, Luis
Belmar, Lara
Gómez Fernández, Cristina
Miranda-Filloy, J. A.
Caminal-Montero, Luis
Collado, Paz
Árgila, Diego de
Quiroga, Patricia
Vicente, Esther
Triguero-Martínez, Ana
Rubio, Esteban
León Luque, Manuel
Blanco-Madrigal, Juan María
Galíndez-Agirregoikoa, E.
Martín, Javier
Gualillo, Oreste
Blanco, Ricardo
Castañeda, Santos
González-Gay, M. A.
López-Mejías, Raquel
Publication Year :
2022

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.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1348917729
Document Type :
Electronic Resource