A. Tsatsoulis et al., INCREASED SERUM INTERLEUKIN-1-BETA DURING TREATMENT OF HYPERTHYROIDISM WITH ANTITHYROID DRUGS, European journal of clinical investigation, 25(9), 1995, pp. 654-658
Citations number
29
Categorie Soggetti
Medicine, Research & Experimental","Medicine, General & Internal
Serum interleukin-1 beta (IL-1 beta) and soluble interleukin-2 recepto
r (sIL-2R) levels were examined in patients with hyperthyroidism due t
o Graves' disease (GD) and toxic nodular goitre (TNG) before and durin
g antithyroid drug therapy. A total of 32 patients were studied; 23 pa
tients (14 with GD and nine with TNG) were in a hyperthyroid state (gr
oup A) and nine patients (four with GD and five with TNG) were in a eu
thyroid state, under carbimazole or methimazole treatment (group B). T
en hyperthyroid patients from group A (seven with GD and three with TN
G) were also examined while euthyroid on treatment (Subgroup A). Serum
was taken from all patients for the measurement of sIL-2R, IL-1 beta,
total T-4 (TT4), total T-3 (TT3) and TSH concentrations. The results
were compared with those from 30 normal controls. Serum sIL-2R levels
were higher in Group A (671.3 +/- 74.0 U mL(-1), mean +/- SE), than in
Group B (214.1 +/- 61.8 U mL(-1)) and controls (149 +/- 14.8 U mL(-1)
), P < 0.001. Similarly, the subgroup of 10 patients had higher levels
of sIL-2R during the hyperthyroid phase than while euthyroid (P < 0.0
01). There was a positive correlation between sIL-2R values and levels
of T-4 and T-3. In contrast, serum IL-1 beta levels were higher in Gr
oup B patients (197.5 +/- 39.2 pg mL(-1)) compared with those in Group
A (66.5 +/- 17 pg mL(-1), P < 0.01). IL-1 beta levels were also highe
r in Subgroup A patients during the euthyroid than in the hyperthyroid
phase of their disease (P < 0.005). In comparison with controls mean
IL-1 beta levels were higher in both groups (A and B) of patients (P <
0.05 and P < 0.002, respectively). It is concluded that serum IL-1 be
ta, as well as sIL-2R is elevated in hyperthyroid patients. During tre
atment with antithyroid drugs sIL-2R returns to normal, but IL-1 beta
increases further. The latter changes may indicate a role for IL-1 bet
a in mediating antithyroid drug action.