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. Author manuscript; available in PMC: 2022 May 6.
Published in final edited form as: Rheumatology (Oxford). 2022 May 5;61(5):2113–2118. doi: 10.1093/rheumatology/keab651

Table 1. MS and inflammatory measures within the CSA-cohort (A) and patients who progressed to RA (B).

(A) Complete cohort (n=575) OR (95%CI) (B) RA-subgroup (n=76) OR (95%CI)
Univariable:
Increased CRP 1.93 (1.30-2.88) 3.86 (1.45-10.24)
Any subclinical inflammation + 1.34 (0.95-1.89) 5.00 (0.99-24.41)
Subclinical synovitis + 1.95 (1.32-2.87) 2.56 (1.04-6.52)
Subclinical tenosynovitis + 1.59 (1.10-2.31) 3.09 (0.99-9.60)
Subclinical osteitis + 1.14 (0.76-1.72) 1.50 (0.59-3.84)
Multivariable #:
Increased CRP 1.78 (1.17-2.69) 3.24 (1.13-9.25)
Subclinical synovitis + 1.77 (1.16-2.69) 2.07 (0.73-5.87)
Subclinical tenosynovitis + 1.13 (0.75-1.72) 1.47 (0.40-5.49)
Multivariable *:
Increased CRP 1.79 (1.18-2.72) 10.57 (2.27-49.17)
Subclinical synovitis + 1.69 (1.10-2.58) 1.63 (0.52-5.09)
Subclinical tenosynovitis + 1.23 (0.80-1.91) 1.76 (0.42-7.35)

Increased CRP: C-reactive protein (increased if ≥5 mg/L), +: presence of an MRI-feature, ACPA: anti-citrullinated peptide antibody (anti-CCP2, positive if ≥7U/mL), 95% CI: 95% confidence interval

#

Independent variables: increased CRP, subclinical synovitis + and subclinical tenosynovitis +.

*

Independent variables: increased CRP, subclinical synovitis + and subclinical tenosynovitis +, age and gender.

Explained variance (Nagelkerke R2) of the multivariable model (#) in the complete cohort was 5% and increased to 18% in the RA-subgroup.