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. 2019 Jan 22;5(1):e000836. doi: 10.1136/rmdopen-2018-000836

Table 2.

Longitudinal effect of MTX plus bDMARD combination therapy compared with bDMARD monotherapy

Outcome DAS28*
β (95% CI)
RAPID3*
β (95% CI)
DAS28 <2.6†
OR (95% CI)
RAPID3 ≤3.0†
β (95% CI)
SJC*
β (95% CI)
ESR*
β (95% CI)
TJC*
β (95% CI)
PGA*
β (95% CI)
Basic model‡ 0.39 (−0.65 to −0.13) −0.60 (−1.71 to 0.52) 1.63 (1.10 to 2.42) 1.17 (0.53 to 2.57) 1.10 (−2.10 to −0.19) −2.59 (−5.60 to 0.41) −0.47 (−1.75 to 0.82) −0.11 (−0.59 to 0.38)
Adjusted model§ 0.42 (−0.67 to −0.17) −0.58 (−0.65 to 049) 1.55 (1.03 to 2.31) 1.16 (0.55 to 2.42) 0.91 (−1.77 to −0.06) −1.90 (−4.87 to 1.08) −0.52 (−1.84 to 0.80)

*Linear longitudinal generalised estimating equation (GEE) models were used for continuous outcomes; numbers shown are continuous status scores.

†Logistic longitudinal GEE models were used for binominal variables; numbers shown are ORs.

‡Non-adjusted model.

§Model of each component was adjusted for a priori selected possible confounders: age, gender, drugs for comorbidities (1/0), oral glucocorticosteroids (1/0) and use of non-steroidal anti-inflammatory drugs.

¶No result; model failed to converge.

**Statistical significant results shown in bold.

DAS28, 28-joint Disease Activity Score; ESR, erythrocyte sedimentation rate; MTX, methotrexate; PGA, patient global assessment; RAPID3, Routine Assessment of Patient Index Data 3; SJC, swollen joint count; TJC, tender joint count; bDMARD, biological disease-modifying antirheumatic drug.