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. 2014 Mar 3;2014:681635. doi: 10.1155/2014/681635

Table 4.

Biochemical markers of inflammatory activity and endothelial activation according to DAS28.

Control group (n = 29) RA patients with low DAS28 (n = 15) RA patients with high DAS28 (n = 11) P valueua P adjusteda
Nv Mean (SD) Nv Mean (SD) Nv Mean (SD)
ADMA, µmol/L 28 0.67 (0.18) 15 0.69 (0.17) 11 0.88 (0.19)∗#‡¥ 0.007 0.027
SDMA, µmol/L 26 0.62 (0.18) 15 0.58 (0.18) 11 0.53 (0.13) 0.404 0.220
ADMA/SDMA ratio 26 1.17 (0.47) 15 1.27 (0.4)* 11 1.77 (0.69)∗‡¥ 0.006 0.020
sVCAM-1, ng/mL 28 613.3 (148.4) 15 779.98 (203.67)∗‡ 11 685.61 (156.74) 0.008 0.033
MCP-1, pg/mL 28 262.4 (90.73) 15 336.13 (87.84) 11 493.47 (379.53)∗‡ 0.015 0.030
sE-selectin, ng/mL 28 12.45 (8.02) 15 14.98 (5.8) 11 22.03 (10.9)∗‡¥ 0.006 0.047
vWf, % 27 73.73 (22.39) 15 102.76 (44.78)∗‡ 11 121.19 (54.51)∗‡ 0.008 0.019
Osteoprotegerin, pmol/L 28 4.01 (1.06) 15 4.89 (0.98) 11 5.65 (1.76)∗‡ 0.001 0.038
Pentraxin-3, ng/mL 28 0.45 (0.17) 15 0.73 (0.27)∗‡ 11 0.75 (0.31)∗‡ 0.001 0.002
ESR, mm/h 29 6.58 (4.79) 14 21.64 (16.94)∗‡ 11 61.27 (22.93)∗#‡¥ <0.001 <0.001
hsCRP, mg/L 29 0.84 (0.71) 15 4.48 (6.2) 11 32.9 (32.84)∗#‡¥ 0.004 <0.001
TNF-α, pg/mL 28 1.78 (1.07) 15 2.06 (0.53) 11 3.33 (1.24)∗#‡¥ <0.001 <0.001
Interleukin-6, pg/mL 28 0.86 (0.41) 15 4.54 (5.11)* 11 14.93 (8.72)∗#‡¥ <0.001 <0.001

Data are shown as unadjusted means (SD).

Low DAS28 = (2.6–5.1); high DAS28 = (>5.1).

Nv: valid cases; RA: rheumatoid arthritis; ADMA: asymmetric dimethyl-L-arginine; SDMA: symmetric dimethyl-L-arginine; sVCAM-1: soluble vascular cell adhesion molecule-1; MCP-1: monocyte chemotactic protein-1; sE-selectin: soluble E-selectin; vWF: von Willebrand factor.

uaUnadjusted P value in ANOVA (GLM models). *P < 0.05 versus control group and # P < 0.05 versus RA patients with low disease activity in post hoc analyses for unadjusted ANOVA.

aAge-sex adjusted Pvalue for the defining groups of patients in ANOVA (GLM models)—type III sum of square (SS) was used.

P < 0.05 versus control group and ¥ P ≤ 0.05 versus RA patients with low disease activity in post hoc analyses for adjusted ANOVA.