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Influence of MUC5B gene on antisynthetase syndrome

Author
López Mejías, Raquel; Remuzgo Martínez, Sara; Genre, Fernanda; Pulito Cueto, Verónica; Fernández Rozas, Sonia M.; Llorca, Javier; Iturbe Fernández, David; Mora Cuesta, Víctor M.; Ortego Centeno, Norberto; Pérez Gómez, Nair; Mera-Varela, Antonio; Martínez-Barrio, Julia; López-Longo, Francisco Javier; Mijares, Verónica; Lera-Gómez, Leticia; Usetti, Maria Piedad; Laporta, Rosalía; Pérez, Virginia; De Pablo Gafas, Alicia; Alfranca González, Arantzazuuntranslated; Calvo-Alén, Jaime; Romero-Bueno, Fredeswinda; Sánchez-Pernaute, Olga; Nuno, Laura; Bonilla, Gema; Balsa Criado, Alejandrountranslated; Hernández-González, Fernanda; Grafia, Ignacio; Prieto-González, Sergio; Narváez, Javier; Trallero-Araguas, Ernesto; Selva-O’Callaghan, Albert; Gualillo, Oreste; Castañeda Sanz, Santosuntranslated; Cavagna, Lorenzo; Cifrian, José M.; González-Gay, Miguel A.
Entity
UAM. Departamento de Medicina; Instituto de Investigación Sanitaria Fundación Jiménez Díaz (IIS-FJD); Instituto de Investigación Sanitaria Hospital Universitario de La Princesa (IIS-IP)
Publisher
Nature Research
Date
2020-01-29
Citation
10.1038/s41598-020-58400-0
Scientific Reports 10 (2019): 1415
 
 
 
ISSN
2045-2322
DOI
10.1038/s41598-020-58400-0
Funded by
This study was partially supported by grants from the Foundation for Research in Rheumatology (FOREUM). RL-M is a recipient of a Miguel Servet type I programme fellowship from the ‘Instituto de Salud Carlos III’ (ISCIII), cofunded by the European Social Fund (ESF, ‘Investing in your future’) (grant CP16/00033). SR-M is supported by funds of the RETICS Program (RD16/0012/0009), co-funded by the European Regional Development Fund (ERDF). VP-C is supported by a pre-doctoral grant from IDIVAL (PREVAL 18/01). VM is supported by funds of a Miguel Servet type I programme (grant CP16/00033) (ISCIII, co-funded by ESF). LL-G is supported by funds of PI18/00042 (ISCIII, co-funded by ERDF). OG is Staff Personnel of Xunta de Galicia (Servizo Galego de Saude, SERGAS) through a research-staff stabilization contract (ISCIII/SERGAS). OG,is member of RETICS Programme, RD16/0012/0014 (RIER: Red de Investigación en Inflamación y Enfermedades Reumáticas) via Instituto de Salud Carlos III (ISCIII) and FEDER. The work of OG (PI17/00409), was funded by Instituto de Salud Carlos III and FEDER. OG is a beneficiary of a project funded by Research Executive Agency of the European Union in the framework of MSCA-RISE Action of the H2020 Programme (Project number 734899). OG is beneficiary of a grant funded by Xunta de Galicia, Consellería de Educación, Universidade e Formación Profesional and Consellería de Economía, Emprego e Industria (GAIN), GPC IN607B2019/10
Project
Gobierno de España. CP16/00033
Editor's Version
http://doi.org/10.1038/s41598-020-58400-0
Subjects
interstitial lung-disease; promoter polymorphism; pulmonary-fibrosis; systemic-sclerosis; pneumonias; features; pattern; cohort; mucins; Medicina
URI
http://hdl.handle.net/10486/692628
Rights
© 2020 The Authors

Licencia Creative Commons
Esta obra está bajo una Licencia Creative Commons Atribución 4.0 Internacional.

Abstract

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
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Google™ Scholar:López Mejías, Raquel - Remuzgo Martínez, Sara - Genre, Fernanda - Pulito Cueto, Verónica - Fernández Rozas, Sonia M. - Llorca, Javier - Iturbe Fernández, David - Mora Cuesta, Víctor M. - Ortego Centeno, Norberto - Pérez Gómez, Nair - Mera-Varela, Antonio - Martínez-Barrio, Julia - López-Longo, Francisco Javier - Mijares, Verónica - Lera-Gómez, Leticia - Usetti, Maria Piedad - Laporta, Rosalía - Pérez, Virginia - De Pablo Gafas, Alicia - Alfranca González, Arantzazu - Calvo-Alén, Jaime - Romero-Bueno, Fredeswinda - Sánchez-Pernaute, Olga - Nuno, Laura - Bonilla, Gema - Balsa Criado, Alejandro - Hernández-González, Fernanda - Grafia, Ignacio - Prieto-González, Sergio - Narváez, Javier - Trallero-Araguas, Ernesto - Selva-O’Callaghan, Albert - Gualillo, Oreste - Castañeda Sanz, Santos - Cavagna, Lorenzo - Cifrian, José M. - González-Gay, Miguel A.

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  • Producción científica en acceso abierto de la UAM [16828]

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