Influence of the FCGR2A rs1801274 and FCGR3A rs396991 Polymorphisms on Response to Abatacept in Patients with Rheumatoid Arthritis.

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.accessioned2025-01-07T14:27:27Z
dc.date.available2025-01-07T14:27:27Z
dc.date.issued2021-06-18
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 low-affinity 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.
dc.identifier.doi10.3390/jpm11060573
dc.identifier.issn2075-4426
dc.identifier.pmcPMC8233911
dc.identifier.pmid34207385
dc.identifier.pubmedURLhttps://pmc.ncbi.nlm.nih.gov/articles/PMC8233911/pdf
dc.identifier.unpaywallURLhttps://www.mdpi.com/2075-4426/11/6/573/pdf?version=1624023536
dc.identifier.urihttps://hdl.handle.net/10668/26404
dc.issue.number6
dc.journal.titleJournal of personalized medicine
dc.journal.titleabbreviationJ Pers Med
dc.language.isoen
dc.organizationSAS - Hospital Universitario Virgen de las Nieves
dc.organizationSAS - Hospital Universitario San Cecilio
dc.organizationSAS - Hospital de Poniente
dc.organizationSAS - Hospital Universitario Virgen de las Nieves
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectFCGR2A
dc.subjectFCGR3A
dc.subjectabatacept
dc.subjecteffectiveness
dc.subjectpolymorphisms
dc.subjectrheumatoid arthritis
dc.titleInfluence of the FCGR2A rs1801274 and FCGR3A rs396991 Polymorphisms on Response to Abatacept in Patients with Rheumatoid Arthritis.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number11

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