Table 2

Results of FDG-PET/CT scans target to background ratio comparing subjects randomised to TNF inhibitors versus triple therapy

Arterial location assessedBaselineFollow-upDifferences (Δ=baseline to follow-up)
TNFiTriple therapyTNFiTriple therapyΔTNFiΔTriple therapyTNFi versus triple therapyP value
Mean (SD)β (95% CI)
Primary outcome
 MDS of index vessel*2.72 (0.75)2.62 (0.51)2.47 (0.68)2.43 (0.51)−0.24 (0.51)−0.19 (0.51)−0.02 (−0.19 to 0.15)0.79
Secondary outcomes†
 MDS of aorta2.67 (0.79)2.64 (0.50)2.50 (0.69)2.47 (0.42)−0.17 (0.52)−0.17 (0.39)0.01 (−0.14 to 0.17)0.87
 Aorta2.46 (0.66)2.48 (0.43)2.45 (0.74)2.42 (0.38)−0.02 (0.43)−0.06 (0.34)0.03 (−0.11 to 0.18)0.64
 Bilateral carotids2.13 (0.36)2.21 (0.44)2.07 (0.51)2.11 (0.46)−0.06 (0.48)−0.10 (0.51)−0.003 (−0.20 to 0.19)0.98
 Index vessel2.51 (0.62)2.45 (0.45)2.43 (0.74)2.38 (0.47)−0.09 (0.43)−0.07 (0.47)−0.01 (−0.17 to 0.16)0.94
  • Follow-up value is at study conclusion (approximately 24 weeks). Triple therapy refers to the use of weekly methotrexate, sulfasalazine 1000 mg two times per day, and hydroxychloroquine 200–400 mg per day. Counts of the number of individuals included in each analysis: TBR MDS—TNFi=58, triple therapy=57; aorta—TNFi=56, triple therapy=52; left carotid—TNFi=44, triple therapy=41; right carotid—TNFi=43, triple therapy=42; average carotid—TNFi=45, triple therapy=43.

  • *When vessel is not specified, the measurement refers to the index vessel with the most diseased segment.

  • †P values for the secondary outcomes are nominal and not corrected for multiple testing. All β estimates and p values are from ANCOVA models that estimate the change in TBR as a function of the baseline TBR, treatment group and the randomisation strata.

  • ANCOVA, analysis of covariance; FDG-PET/CT, 18F-fluorodeoxyglucose positron emission tomography/CT scan; MDS, most disease segment examining right and left carotid arteries and aorta; TBR, target to background ratio; TNFi, TNF inhibitor.