Mostrar el registro sencillo del ítem

dc.contributor.authorMárquez Pete, Noelia
dc.contributor.authorMaldonado Montoro, María del Mar
dc.contributor.authorPérez Ramírez, Cristina 
dc.contributor.authorMartínez Martínez, Fernando 
dc.contributor.authorMartínez de la Plata, Juan Enrique 
dc.contributor.authorDaddaoua, Abdelali 
dc.contributor.authorJiménez Morales, Alberto
dc.date.accessioned2021-07-01T10:27:49Z
dc.date.available2021-07-01T10:27:49Z
dc.date.issued2021
dc.identifier.citationMárquez Pete, N.; Maldonado Montoro, M.d.M.; Pérez Ramírez, C.; Martínez Martínez, F.; Martínez de la Plata, J.E.; Daddaoua, A.; Jiménez Morales, A. Influence of the FCGR2A rs1801274 and FCGR3A rs396991 Polymorphisms on Response to Abatacept in Patients with Rheumatoid Arthritis. J. Pers. Med. 2021, 11, 573. https://doi.org/ 10.3390/jpm11060573es_ES
dc.identifier.urihttp://hdl.handle.net/10481/69456
dc.description.abstractAbatacept (ABA) is an immunosuppressant indicated for treatment of rheumatoid arthritis (RA). Effectiveness might be influenced by clinical RA variants and single-nucleotide polymorphisms (SNPs) in genes encoding protein FCGR2A (His131Arg) and FCGR3A (Phe158Val) involved in pharmacokinetics of ABA. An observational cohort study was conducted in 120 RA Caucasian patients treated with ABA for 6 and 12 months. Patients with the FCGR2A rs1801274-AA genotype (FCGR2A-p.131His) showed a better EULAR response (OR = 2.43; 95% CI = 1.01–5.92) at 12 months and low disease activity (LDA) at 6 months (OR = 3.16; 95% CI = 1.19–8.66) and 12 months (OR = 6.62; 95% CI = 1.25–46.89) of treatment with ABA. A tendency was observed towards an association between the FCGR3A rs396991-A allele (FCGR3A-p.158Phe) and better therapeutic response to ABA after 12 months of treatment (p = 0.078). Moreover, we found a significant association between the lowaffinity FCGR2A/FCGR3A haplotypes variable and LDA after 12 months of ABA treatment (OR = 1.59; 95% CI = 1.01–2.58). The clinical variables associated with better response to ABA were lower age at starting ABA (OR = 1.06; 95% CI = 1.02–1.11) and greater duration of ABA treatment (OR = 1.02; 95% CI = 1.01–1.04), lower duration of previous biological therapies (OR = 0.99; 95% CI = 0.98–0.99), non-administration of concomitant disease-modifying antirheumatic drugs (DMARDs) (OR = 24.53; 95% CI = 3.46–523.80), non-use of concomitant glucocorticoids (OR = 0.12; 95% CI = 0.02–0.47), monotherapy (OR = 19.22; 95% CI = 2.05–343.00), lower initial patient’s visual analogue scale (PVAS) value (OR = 0.95; 95% CI = 0.92–0.97), and lower baseline ESR (OR = 0.92; 95% CI = 0.87–0.97). This study showed that high-affinity FCGR2A-p.131His variant, low-affinity FCGR3A-p.158Phe variant, and combined use of FCGR2A/FCGR3A genetic variations could affect ABA effectiveness. Further studies will be required to confirm these results.es_ES
dc.description.sponsorshipFundación de Investigación Biosanitaria de Andalucía Oriental (FIBAO)es_ES
dc.description.sponsorshipUniversity of Granadaes_ES
dc.description.sponsorshipERDF funds (EU) from the Instituto de Salud Carlos III (PT13/0010/0039es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAtribución 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectRheumatoid arthritis es_ES
dc.subjectAbataceptes_ES
dc.subjectFCGR2Aes_ES
dc.subjectFCGR3Aes_ES
dc.subjectEffectivenesses_ES
dc.subjectPolymorphismses_ES
dc.titleInfluence of the FCGR2A rs1801274 and FCGR3A rs396991 Polymorphisms on Response to Abatacept in Patients with Rheumatoid Arthritises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.3390/jpm11060573


Ficheros en el ítem

[PDF]

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem

Atribución 3.0 España
Excepto si se señala otra cosa, la licencia del ítem se describe como Atribución 3.0 España