Influence of the FCGR2A rs1801274 and FCGR3A rs396991 Polymorphisms on Response to Abatacept in Patients with Rheumatoid Arthritis
Metadatos
Afficher la notice complèteAuteur
Márquez Pete, Noelia; Maldonado Montoro, María del Mar; Pérez Ramírez, Cristina; Martínez Martínez, Fernando; Martínez de la Plata, Juan Enrique; Daddaoua, Abdelali; Jiménez Morales, AlbertoEditorial
MDPI
Materia
Rheumatoid arthritis Abatacept FCGR2A FCGR3A Effectiveness Polymorphisms
Date
2021Referencia bibliográfica
Márquez 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/jpm11060573
Patrocinador
Fundación de Investigación Biosanitaria de Andalucía Oriental (FIBAO); University of Granada; ERDF funds (EU) from the Instituto de Salud Carlos III (PT13/0010/0039Résumé
Abatacept (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.