Pa. Merkel et al., INTERLEUKIN-2 RECEPTOR LEVELS IN SERA OF PATIENTS WITH RHEUMATOID-ARTHRITIS TREATED WITH SULFASALAZINE, PARENTERAL GOLD, OR PLACEBO, Journal of rheumatology, 23(11), 1996, pp. 1856-1861
Objective. To evaluate the associations of soluble serum interleukin-2
receptor (sIL-2R) levels in patients with rheumatoid arthritis (RA) w
ith clinical and laboratory measures of disease activity and the predi
cted response to therapy. Methods. sIL-2R levels were determined by EL
ISA in 137 patients with RA, not previously treated with 2nd line ther
apy. Patients were enrolled in a prospective, randomized, placebo cont
rolled trial of sulfasalazine (SSZ) versus gold sodium thiomalate (GST
M), sponsored by the Cooperative Systematic Studies of Rheumatic Disea
ses. Using correlation analysis and regression modeling, the clinical
utility of sIL-2R as a measure of disease activity and predictor of ou
tcome was assessed. Results. 91 women and 46 men with a mean age of 51
+/- 13 years and mean duration of disease of 64 +/- 78 months partici
pated in this study, The mean sIL-2R level in all patients with RA was
markedly elevated (980 +/- 589 U/ml) compared with that in healthy co
ntrol subjects (446 +/- 196 U/ml; p = < 0.0001). There was no correlat
ion between the sIL-2R levels and the joint pain/tenderness count, eit
her at study entry or completion. There were significant positive corr
elations between the baseline sIL-2R and baseline erythrocyte sediment
ation rate (ESR) and between the change in sIL-2R and the change in ES
R. Both a multiple linear regression model and a multiple logistic reg
ression model showed that baseline sIL-2R levels were not predictive o
f clinical outcome, Conclusion, sIL-2R levels are significantly elevat
ed in patients with active RA and correlate positively with ESR. Howev
er, these results indicate that in patients with early RA, sIL-2R leve
ls are neither associated with standard disease activity criteria nor
predictive of the response to therapy with SSZ or GSTM, even after con
trolling for the simultaneous effects of other important clinical vari
ables.