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. 2024 Mar 5;26:61. doi: 10.1186/s13075-024-03295-9

Table 2.

Impacts of 24 weeks therapies of DMARDs on urinary PGIM, TXBM, 12-HETE and LTE4

PGIM TXBM 12-HETE LTE4
Day 0 Week 24 Pa Day 0 Week 24 Pa Day 0 Week 24 Pb Day 0 Week 24 Pb
Total 25.66% 40.79% 0.069 43.42% 69.74% 0.056 67.53.% 72.73% 0.419 23.38% 28.57% 0.669
ACT 28.95% 50.00% 0.172 65.79% 76.32% 0.723 63.16% 78.95% 0.098 23.68% 26.32% 0.904
CZP 19.05% 30.95% 0.320 16.67% 61.90% < 0.001 Not measured
ABA 38.46% 51.28% 0.194 66.67% 82.05% 0.131 71.79% 66.67% 0.653 23.08% 30.77% 0.588
TCZ 15.15% 30.30% 0.218 24.24% 57.58% 0.019 Not measured

ACT, Active Conventional Therapy arm; CZP, Certolizumab Pegol arm; ABA, Abatacept arm; TCZ, Tocilizumab arm; PGIM, 2,3-dinor-6-keto-PGF; TXBM, 2,3-dinor-TXB2, 12-HETE, 12-Hydroxyeicosatetraenoic Acid; LTE4, Leukotriene E4; GEE, Generalized Estimating Equations

P values were obtained from the following statistical tests:

aGEE model adjusted for use of NSAIDs and creatinine concentrations

bGEE model adjusted for creatinine concentrations