Celal Bayar University, Medical Faculty, Department of Internal Medicine, Division of Endocrinology, Manisa, Turkiye.
Eur Cytokine Netw. 2009 Mar;20(1):27-32. doi: 10.1684/ecn.2009.0147.
Hashimoto's thyroiditis is a chronic, organ-specific autoimmune disease. It is the most common cause of primary hypothyroidism during the adolescent period, via autoimmune thyroid tissue destruction, affecting 2% of the population. The pathogenesis of Hashimoto's thyroiditis involves a complex interaction between predisposing genetic and environmental factors.
In this study, we wanted to investigate the role of cytokines such as IL-2, IL-4, IL-12 and IFN-gamma in the pathogenesis of the disease, and the changes to cytokine levels brought about by treatment with L-thyroxine.
Sixty five female patients, aged 18-73 years with Hashimoto's thyroiditis, referred to the Celal Bayar University Medical Faculty Endocrinology out-patients clinic, were included in this study. After a 10-12 week period of L-thyroxine treatment, all patients were restored to the euthyroid state. At the beginning and end of the treatment period, serum-free triiodothyronine (FT3), free thyroxine (FT4), thyroid-stimulating hormone (TSH), autoantibodies against thyroid peroxidase (anti-TPO), autoantibodies against thyroglobulin (anti-Tg) levels were measured using a chemiluminecent, immunometric method, and cytokine levels were measured using ELISA.
There was a statistically significant decrease in the serum levels of TSH (p < 0.0001) and a concomitant increase in FT4 serum levels (p < 0.0001). Also, during the post-treatment period, serum levels of anti-Tg (p < 0.01) and anti-TPO (p < 0.001) were significantly lower than during the pre-treatment period. A statistically significant decrease was shown for interleukin (IL)-12 serum levels during the post-treatment period (p < 0.001). However, the decrease in interferon (IFN)-gamma serum levels was not statistically significant (p = 0.276). On the other hand, no change was demonstrated in serum IL-2 and IL-4 levels (p = 0.953 and p = 0.313, respectively) after treatment with L-thyroxine.
Considering that our study involved a 10-12 week period of treatment, the statistically significant decrease in serum IL-12 levels, and the statistically non-significant decrease in IFN-gamma levels, might indicate that a T helper type 1 inflammatory process had been halted or slowed down.
桥本甲状腺炎是一种慢性、器官特异性自身免疫性疾病。它是青少年时期原发性甲状腺功能减退症最常见的原因,通过自身免疫性甲状腺组织破坏,影响 2%的人群。桥本甲状腺炎的发病机制涉及到易感性遗传和环境因素的复杂相互作用。
在本研究中,我们希望研究细胞因子如白细胞介素-2(IL-2)、白细胞介素-4(IL-4)、白细胞介素-12(IL-12)和干扰素-γ(IFN-γ)在疾病发病机制中的作用,以及左旋甲状腺素治疗引起的细胞因子水平的变化。
65 名年龄在 18-73 岁的女性桥本甲状腺炎患者被纳入本研究。这些患者均来自 Celal Bayar 大学医学系内分泌科门诊。在接受 10-12 周的左旋甲状腺素治疗后,所有患者均恢复到甲状腺功能正常状态。在治疗开始和结束时,使用化学发光免疫测定法测量血清游离三碘甲状腺原氨酸(FT3)、游离甲状腺素(FT4)、促甲状腺激素(TSH)、甲状腺过氧化物酶自身抗体(抗 TPO)和甲状腺球蛋白自身抗体(抗 Tg)水平,使用酶联免疫吸附试验(ELISA)测量细胞因子水平。
TSH 血清水平显著下降(p<0.0001),FT4 血清水平升高(p<0.0001)。此外,在治疗后,抗 Tg(p<0.01)和抗 TPO(p<0.001)血清水平显著低于治疗前。IL-12 血清水平在治疗后显著下降(p<0.001)。然而,干扰素(IFN)-γ血清水平的下降无统计学意义(p=0.276)。另一方面,甲状腺素治疗后,血清白细胞介素(IL)-2 和 IL-4 水平无变化(p=0.953 和 p=0.313)。
考虑到我们的研究涉及 10-12 周的治疗期,IL-12 血清水平的显著下降和 IFN-γ 水平的非统计学显著下降可能表明辅助性 T 细胞 1 型炎症过程已经停止或减缓。