Table 1

Baseline characteristics and disease evolution of the ESPOIR patients who received MTX or its equivalent, LEF, as a first-line biologic agent for RA, and radiographic structural damage progression during the first year in the cohort

ESPOIR cohort patients who received MTX or LEF
CharacteristicsAll (n=370)RRP+ (n=41)RRP− (n=329)
Age, years49.4±11.4 (51.5)50.2±10.8 (52.1)49.3±11.5 (51.4)
Female sex271 (73.2%)31 (75.6%)240 (73%)
Disease duration, weeks*15.2±8.2 (13.6)18.6±8.4 (18.6)14.7±8.1 (13)
2010 ACR/EULAR criteria316 (85.4%)38 (92.7%)278 (84.5%)
Swollen joint count in 28 joints7.9±5.4 (7)8.7±6.1 (8)7.8±5.3 (7)
Tender joint count in 28 joints8.7±6.9 (7)8.3±6.3 (7)8.7±6.9 (7)
ESR, mm/1st h32.7±25 (26)32.6±21.0 (30)32.7±25.4 (25)
CRP, mg/L24.8±37.7 (11)26.0±27.9 (14)24.6±38.7 (11)
DAS285.3±1.2 (5.2)5.3±1.2 (5.4)5.3±1.2 (5.2)
IgM RF positivity*204 (55.1%)29 (70.7%)175 (53.2%)
ACPA positivity*185 (50%)31 (75.6%)154 (46.8%)
HAQ score1.0±0.7 (1)1.0±0.6 (1)1.0±0.7 (1)
Typical RA erosion66 (17.8%)18 (44%)48 (14.6%)
Duration of DMARD during first year, months9.06± (3.07)9.07± (3.20)8.98± (3.06)
Concomitant glucocorticoids98 (26%)7 (17.1%)91 (27.7%)
vSHS baseline total score*4.5±6.8 (2)10.8±9.8 (9)3.7±5.8 (2)
ΔvSHS total1.6±5.4 (0)12.9±8.0 (10)0.2±2.8 (0)
Progressors (ΔvSHS≥1)126 (34.1%)41 (100%)85 (25.8%)
  • *Significant difference between RRP+ and RRP− (p value <0.05).

  • Data are mean±SD (median) or no. (%).

  • ACPA, anti-citrullinated protein antibody (ELISA, DiaSorin, France; positive >50 U/mL); ACR/EULAR, American College of Rheumatology/European League Against Rheumatism; CRP, C reactive protein (normally <10 mg/L); DAS28, Disease Activity Score in 28 joints; DMARD, disease-modifying anti-rheumatic drug; ESR, erythrocyte sedimentation rate; HAQ, Health Assessment Questionnaire; LEF, leflunomide; MTX, methotrexate; RA, rheumatoid arthritis; RF, rheumatoid factor (ELISA, Menarini, France; positive >9 UI/mL); RRP, rapid radiographic progression; vSHS, van der Heijde-modified Sharp score.