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Influence of MUC5B gene on antisynthetase syndrome

MUC5B rs35705950 (G/T) is strongly associated with idiopathic pulmonary fibrosis (IPF) and also contributes to the risk of interstitial lung disease (ILD) in rheumatoid arthritis (RA-ILD) and chronic hypersensitivity pneumonitis (CHP). Due to this, we evaluated the implication of MUC5B rs35705950 in...

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Detalles Bibliográficos
Autores principales: López-Mejías, Raquel, Remuzgo-Martínez, Sara, Genre, Fernanda, Pulito-Cueto, Verónica, Rozas, Sonia M. Fernández, Llorca, Javier, Fernández, David Iturbe, Cuesta, Víctor M. Mora, Ortego-Centeno, Norberto, Gómez, Nair Pérez, Mera-Varela, Antonio, Martínez-Barrio, Julia, López-Longo, Francisco Javier, Mijares, Verónica, Lera-Gómez, Leticia, Usetti, María Piedad, Laporta, Rosalía, Pérez, Virginia, Gafas, Alicia De Pablo, González, María Aránzazu Alfranca, Calvo-Alén, Jaime, Romero-Bueno, Fredeswinda, Sanchez-Pernaute, Olga, Nuno, Laura, Bonilla, Gema, Balsa, Alejandro, Hernández-González, Fernanda, Grafia, Ignacio, Prieto-González, Sergio, Narvaez, Javier, Trallero-Araguas, Ernesto, Selva-O’Callaghan, Albert, Gualillo, Oreste, Castañeda, Santos, Cavagna, Lorenzo, Cifrian, José M., González-Gay, Miguel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6989632/
https://www.ncbi.nlm.nih.gov/pubmed/31996780
http://dx.doi.org/10.1038/s41598-020-58400-0
Descripción
Sumario:MUC5B rs35705950 (G/T) is strongly associated with idiopathic pulmonary fibrosis (IPF) and also contributes to the risk of interstitial lung disease (ILD) in rheumatoid arthritis (RA-ILD) and chronic hypersensitivity pneumonitis (CHP). Due to this, we evaluated the implication of MUC5B rs35705950 in antisynthetase syndrome (ASSD), a pathology characterised by a high ILD incidence. 160 patients with ASSD (142 with ILD associated with ASSD [ASSD-ILD+]), 232 with ILD unrelated to ASSD (comprising 161 IPF, 27 RA-ILD and 44 CHP) and 534 healthy controls were genotyped. MUC5B rs35705950 frequency did not significantly differ between ASSD-ILD+ patients and healthy controls nor when ASSD patients were stratified according to the presence/absence of anti Jo-1 antibodies or ILD. No significant differences in MUC5B rs35705950 were also observed in ASSD-ILD+ patients with a usual interstitial pneumonia (UIP) pattern when compared to those with a non-UIP pattern. However, a statistically significant decrease of MUC5B rs35705950 GT, TT and T frequencies in ASSD-ILD+ patients compared to patients with ILD unrelated to ASSD was observed. In summary, our study does not support a role of MUC5B rs35705950 in ASSD. It also indicates that there are genetic differences between ILD associated with and that unrelated to ASSD.