Evaluation of cytokine profiles in rheumatoid arthritis patients with clinically active disease and normal inflammatory indices

被引:1
|
作者
Alex, Asha M. [1 ,2 ]
Sayles, Harlan [3 ,4 ]
Mikuls, Ted R. [3 ,4 ]
Kerr, Gail S. [1 ,2 ,5 ,6 ]
机构
[1] Medstar Georgetown Univ Hosp, Washington, DC 20007 USA
[2] Washington DC Vet Affairs Med Ctr, Washington, DC 20422 USA
[3] Univ Nebraska Med Ctr, Omaha, NE USA
[4] VA Nebraska Western Iowa Hlth Care Syst, Omaha, NE USA
[5] Howard Univ, Washington, DC 20059 USA
[6] Vet Affairs Med Ctr, Rheumatol Sect, 151K,50 Irving St NW, Washington, DC 20422 USA
关键词
Biomarkers; Cytokine profiles; Disease activity; Rheumatoid arthritis; ACTIVITY SCORE; REMISSION; PROGRESSION; VALIDATION; CHEMOKINES; CRITERIA;
D O I
10.1007/s10067-018-4379-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveTo assess the potential utility of a cytokine measurement in rheumatoid arthritis (RA) patients with active joint disease but normal acute phase reactants (APR).MethodsRA patients in a longitudinal observational registry with available cytokine array data were included. Patients were categorized based on agreement/disagreement of physical examination and APR measurements: concordant high (CH) [high tender and/or swollen joint counts (TJC + SJC >3) and APR (ESR 28mm/h + CRP 1.5mg/L)]; concordant low (CL) [TJC + SJC 3 and normal APR]. Discordant (D) [TJC + SJC >3 and normal APR] patients were stratified into low, medium, and high-disease activity (DL, DM, DH). Weighted-average and log-transformed cytokine scores were calculated based on results of a cytokine array. Chi-square tests compared categorical variables by concordance status; t tests, Wilcoxon rank-sum tests, ANOVA models, and ordinary least squares (OLS) regressions were used to compare continuous measures.ResultsRA patients (n=1467) were predominantly male (91%). Compared to CH patients (n=174), D (n=434) were younger, less frequently seropositive, with lower TJC, SJC, and DAS28-3v scores (p<0.001). Cytokine scores for DL, DM, and DH groups were lower than CH patients (p<0.001) and did not differ between DL, DM, and DH subgroups and were similar to CL (n=356) patients. In multivariable analyses including CH and D patients, log-cytokine score was associated with higher DAS28-3v scores (p=0.029). In multivariable analyses including CL patients, concordance status (p=0.011) and ACPA (p=0.013) were predictors of higher log cytokine score.ConclusionIn this study, cytokine scores did not identify active joint disease in RA patients with normal APR.
引用
收藏
页码:1075 / 1081
页数:7
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