Minelli R, Braverman L E, Giuberti T, Schianchi C, Gardini E, Salvi M, Fiaccadori F, Ugolotti G, Roti E
Centro per lo Studio, Prevenzione, Diagnosi e Cura delle Tireopatie, Università degli Studi di Parma, Italy.
Clin Endocrinol (Oxf). 1997 Sep;47(3):357-61. doi: 10.1046/j.1365-2265.1997.2721081.x.
To determine the effects of pharmacological quantities of iodide (SSKI) on thyroid function in euthyroid patients previously treated with recombinant interferon-alpha (rIFN-alpha) for chronic viral hepatitis B and C (HCV), a cytokine which may induce thyroid dysfunction.
Thyroid function tests were carried out in 16 euthyroid patients, 8 of whom had previously developed thyroid dysfunction during rIFN-alpha therapy for HCV, before, during and after the administration of 10 drops of saturated solution of potassium iodide (SSKI) (approximately 350 mg iodide).
All 16 patients had been treated in the past with rIFN-alpha for HCV. Eight patients had developed rIFN-alpha induced abnormalities in thyroid function (5 inflammatory thyrotoxicosis, 1 Graves' disease, and 2 impaired thyroid organification of iodide) and 8 had not developed thyroid dysfunction.
After baseline serum free T4 (FT4) and free T3 (FT3) concentrations, basal and TRH stimulated TSH concentrations, and TSH-receptor (TSH-R-Ab) and thyroid peroxidase (TPO-Ab) antibodies were measured, 10 drops saturated solution of potassium iodide (SSKI, approximately 350 mg iodide) were given daily for 60 days and the above parameters assessed during and after SSKI was discontinued.
Five of 8 patients with a previous history of rIFN-alpha induced thyroid dysfunction developed mild iodide induced abnormalities of thyroid function (subclinical hypothyroidism (slightly elevated basal and TRH stimulated serum TSH concentrations with normal serum FT4 and FT3 concentrations) or hyperthyroidism) compared with the 8 patients who had no previous evidence of thyroid dysfunction during rIFN-alpha therapy.
In view of the present observations, it is prudent to avoid the administration of excess iodine to euthyroid subjects with a previous episode of thyroid dysfunction during rIFN-alpha therapy, adding a new group of patients susceptible to iodine induced thyroid disease.
确定药理剂量的碘化物(饱和碘化钾溶液,SSKI)对既往因慢性乙型和丙型病毒性肝炎接受重组干扰素-α(rIFN-α)治疗的甲状腺功能正常患者甲状腺功能的影响,rIFN-α这种细胞因子可能诱发甲状腺功能障碍。
对16例甲状腺功能正常的患者进行甲状腺功能测试,其中8例患者既往在rIFN-α治疗丙型肝炎期间出现过甲状腺功能障碍,在给予10滴碘化钾饱和溶液(SSKI,约350mg碘化物)之前、期间和之后进行测试。
所有16例患者既往均接受过rIFN-α治疗丙型肝炎。8例患者出现rIFN-α诱导的甲状腺功能异常(5例炎症性甲状腺毒症、1例格雷夫斯病和2例碘化物甲状腺有机化受损),8例未出现甲状腺功能障碍。
在测定基线血清游离T4(FT4)和游离T3(FT3)浓度、基础和促甲状腺激素释放激素(TRH)刺激后的促甲状腺激素(TSH)浓度以及促甲状腺激素受体(TSH-R-Ab)和甲状腺过氧化物酶(TPO-Ab)抗体后,每日给予10滴碘化钾饱和溶液(SSKI,约350mg碘化物),持续60天,并在停用SSKI期间及之后评估上述参数。
与8例在rIFN-α治疗期间无甲状腺功能障碍证据的患者相比,8例既往有rIFN-α诱导的甲状腺功能障碍病史的患者中有5例出现轻度碘化物诱导的甲状腺功能异常(亚临床甲状腺功能减退(基础和TRH刺激后的血清TSH浓度轻度升高,血清FT4和FT3浓度正常)或甲状腺功能亢进)。
鉴于目前的观察结果,对于既往在rIFN-α治疗期间有过甲状腺功能障碍发作的甲状腺功能正常的受试者,谨慎起见应避免给予过量碘,这增加了一组易患碘诱导甲状腺疾病的患者群体。