Table 4.

Longitudinal model: time-fixed and time-varying predictors of failure to apply T2T-LDA during 2-year followup of the RA BIODAM cohort.

VariablesUnivariable OR (95% CI), N = 544–571Univariable pMultivariable OR (95% CI), N = 554
Age, yrs1.01 (1.00–1.01)0.096¥
Sex, female1.01 (0.81–1.25)0.963
Disease duration, yrs1.00 (0.99–1.02)0.528
Education, yrs0.97 (0.95–1.00)0.032¥
No. comorbidities1.17 (1.08–1.26)< 0.001 1.11 (1.03–1.20)
Current smoker1.24 (1.01–1.53)0.0411.26 (1.03–1.53)
Type of center, academic0.82 (0.67–1.00)0.0500.81 (0.68–0.98)
RF positivity0.63 (0.51–0.77)< 0.001*
ACPA positivity0.57 (0.47–0.70)< 0.001*
RF and/or ACPA positivity0.58 (0.46–0.73)< 0.0010.66 (0.53–0.82)
PtGA (0–10) 1.11 (1.08–1.14)< 0.001¥
PGA (0–10) 1.06 (1.03–1.10)< 0.001¥
Swollen joint count (0–44) 1.00 (0.98–1.02) 0.962
Tender joint count (0–53) 1.03 (1.03–1.04)< 0.0011.02 (1.01–1.03)
ESR, mm/h 1.01 (1.00–1.01)0.013¥
CRP, mg/l 1.00 (0.99–1.00)0.453
HAQ 1.43 (1.26–1.61)< 0.001¥
No. previous csDMARD1.02 (0.94–1.11)0.622
Previous treatment with any csDMARD1.10 (0.91–1.33)0.318
  • Not selected from the univariable analysis (p > 0.20).

  • ¥ Not significant in the multivariable analysis (p > 0.05).

  • Modeled as time-varying.

  • * RF or ACPA positivity entered into multivariate model. Country added as a covariate in all univariable models and in the final multivariable model. Final model also adjusted for type of treatment (csDMARD and/or bDMARD). Values in bold face are statistically significant. T2T: treat-to-target; LDA: low disease activity; RA: rheumatoid arthritis; RF: rheumatoid factor; ACPA: anticitrullinated protein antibody; SKATe6055PtGA: patient’s global assessment; PGA: physician’s global assessment; ESR: erythrocyte sedimentation rate; CRP: C-reactive protein; HAQ: Health Assessment Questionnaire; csDMARD: conventional synthetic disease-modifying antirheumatic drug; bDMARD: biological DMARD.