Table 2.

Associations of patient characteristics with baseline QTc interval.

VariablesUnivariate ModelsExtended MV ModelReduced MV Model
βpβpβp
Age, per year−0.120.48
Male−1.620.73
Any CVD risk factors−3.710.38
RA duration, per month−0.00210.93
RF > 40 units5.750.131.160.74
Anti-CCP > 20 units11.510.0047.940.0388.310.021
DAS28, per unit3.820.012
SJC, per joint1.480.0050.910.181.010.038
TJC, per joint0.670.0900.0910.85
Log SDAI, per unit1.890.60
Log CRP, per mg/dl5.300.0013.740.0163.690.016
√ESR, per mm/h1.480.095
Log MMP-3, per ng/ml8.24< 0.0015.120.0185.160.015
VAS, per mm0.130.074
mVAS, per mm−0.0120.89
HAQ, per unit6.650.0472.870.42
Any DMARD−3.050.51
MTX1.240.76
MTX dose, mg0.420.32
Other DMARD−0.390.94
Prednisolone1.280.73
Prednisolone dose, per mg/day0.810.21
Adjusted R20.239< 0.0010.255< 0.001
  • β coefficients represent the average difference in baseline QTc interval per 1 unit higher of the indicated independent variable from linear regression modeling. The first column of univariate models represents individual models in which the indicated independent variable is the only covariate in the model. The MV models are single models containing each of the listed covariates. R2 represents the proportion of the variability of the baseline QTc interval explained by the covariates in the model. MV: multivariable; RA: rheumatoid arthritis; CVD: cardiovascular disease; RF: rheumatoid factor; anti-CCP: anticyclic citrullinated peptide; DAS28: 28-joint count Disease Activity Score; SJC: swollen joint count; TJC: tender joint count; SDAI: Simplified Disease Activity Index; CRP: C-reactive protein; ESR: erythrocyte sedimentation rate; MMP: matrix metalloproteinase; VAS: visual analog scale; mVAS: modified VAS; DMARD: disease-modifying antirheumatic drug; QTc: corrected electrocardiographic QT interval; HAQ: Health Assessment Questionnaire; MTX: methotrexate.