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诊断时和甲巯咪唑治疗期间甲状腺功能亢进 Graves 病患者血清细胞因子的变化。

Changes of serum cytokines in hyperthyroid Graves' disease patients at diagnosis and during methimazole treatment.

机构信息

Endocrinology, Hospital Servidor Publico Estado de São Paulo-IAMSPE, São Paulo, Brazil.

出版信息

Neuroimmunomodulation. 2011;18(1):45-51. doi: 10.1159/000311519. Epub 2010 Jul 13.

DOI:10.1159/000311519
PMID:20628263
Abstract

OBJECTIVE

Cytokines are involved in the pathogenesis of Graves' disease (GD), but ambiguous serum cytokine results have been described.

METHODS

We studied the changes in serum interleukin (IL)-1β, soluble IL-2 receptor (sIL-2R), IL-5, IL-6 and tumor necrosis factor (TNF)-α concentrations in 29 untreated GD patients before and after restoration of euthyroidism with methimazole (MMI) treatment compared to 25 control subjects. Eleven out of 29 GD patients had active Graves' ophthalmopathy (GO).

RESULTS

Compared to controls, untreated GD patients had significantly higher median levels of serum IL-1β (18.7 vs. 34.0 pg/ml), sIL-2R (292.5 vs. 1,585.0 pg/ml), IL-5 (1.0 vs. 9.0 pg/ml), IL-6 (3.0 vs. 5.0 pg/ml) and TNF-α (8.1 vs. 16.0 pg/ml). In euthyroidism following MMI treatment, concentrations of IL-1β (25.0 pg/ml), sIL-2R (362.0 pg/ml), IL-5 (3.0 pg/ml), IL-6 (3.0 pg/ml) and TNF-α (5.0 pg/ml) declined significantly and were similar to controls. The greatest reductions were noted in sIL-2R (76.9%), TNF-α (68.8%) and IL-5 (66.6%) levels. Serum sIL-2R, IL-5 and TNF-α levels in active GO patients were significantly elevated, but no significant differences were observed in GD patients without GO. Using a multiple linear regression analysis, serum IL-1β was significantly associated with free thyroxine, sIL-2R with triiodothyronine and serum thyrotropin receptor antibody (TRAb) and TNF-α with TRAb.

CONCLUSION

These results support the notion that serum cytokines could be used as a marker of GD activity, and the decrease in cytokine levels might be related to the achievement of euthyroidism and the immunomodulatory effects of MMI treatment.

摘要

目的

细胞因子参与格雷夫斯病(GD)的发病机制,但血清细胞因子结果描述不明确。

方法

我们研究了 29 例未经治疗的 GD 患者在甲巯咪唑(MMI)治疗恢复甲状腺功能正常前后血清白细胞介素(IL)-1β、可溶性 IL-2 受体(sIL-2R)、IL-5、IL-6 和肿瘤坏死因子(TNF)-α浓度的变化,与 25 例对照相比。29 例 GD 患者中有 11 例患有活动性格雷夫斯眼病(GO)。

结果

与对照组相比,未经治疗的 GD 患者血清 IL-1β(18.7 与 34.0 pg/ml)、sIL-2R(292.5 与 1585.0 pg/ml)、IL-5(1.0 与 9.0 pg/ml)、IL-6(3.0 与 5.0 pg/ml)和 TNF-α(8.1 与 16.0 pg/ml)中位数水平明显更高。在 MMI 治疗后甲状腺功能正常时,IL-1β(25.0 pg/ml)、sIL-2R(362.0 pg/ml)、IL-5(3.0 pg/ml)、IL-6(3.0 pg/ml)和 TNF-α(5.0 pg/ml)浓度显著下降,与对照组相似。sIL-2R(76.9%)、TNF-α(68.8%)和 IL-5(66.6%)水平下降最大。活动期 GO 患者血清 sIL-2R、IL-5 和 TNF-α水平明显升高,但无 GO 的 GD 患者无明显差异。采用多元线性回归分析,血清 IL-1β与游离甲状腺素显著相关,sIL-2R 与三碘甲状腺原氨酸和血清促甲状腺素受体抗体(TRAb)相关,TNF-α与 TRAb 相关。

结论

这些结果支持这样一种观点,即血清细胞因子可作为 GD 活动的标志物,细胞因子水平的降低可能与甲状腺功能正常的实现和 MMI 治疗的免疫调节作用有关。

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