Martocchia A, Labbadia G, Paoletti V, Gargano S, Grossi A, Trabace S, Musca A, Falaschi P
Chair of Internal Medicine - II Faculty of Medicine, University of Rome La Sapienza, Italy.
Neuro Endocrinol Lett. 2001;22(1):49-52.
The authors described a case of Hashimoto's disease during interferon-alpha (IFN-alpha) treatment for chronic viral C hepatitis in a patient with the specific genetic susceptibility associated with the thyroid disease.
A 60-year-old woman with chronic active viral C hepatitis (HCV genotype = 3a) started IFN-alpha therapy in November '96. Before treatment thyroid function tests were normal and anti-thyroid (anti-thyroglobulin and anti-thyroid peroxidase) Abs were negative. During IFN therapy, serum aminotransferases fell within the normal range and viremia (serum HCV-RNA) became negative after one year. After 20 months, the patient presented clinical features of primary hypothyroidism. Anti-thyroid Abs were found positive. Hormonal, ultrasonographic, radioiodine scanning and fine needle aspiration findings were consistent with the diagnosis of Hashimoto's thyroiditis. The tissutal typing of the patient showed the presence of Human Leukocyte Antigen (HLA) DRB1*11 gene (corresponding to DR5 antigen). IFN-alpha therapy was suspended and a treatment with l-T4 started. Chronic viral infection relapsed after the suspension of the IFN-alpha therapy.
This case report showed that the clinical appearance of Hashimoto's disease after IFN-alpha therapy for chronic C hepatitis in our patient was associated with a specific genetic predisposition (DR5) for this pathology. Further studies are necessary to evaluate whether the study of HLA antigens may be a very useful tool to detect the patients with a predisposition to develop autoimmune thyroiditis, in order to make a early diagnosis of thyroid disorders during the IFN-alpha treatment.
作者描述了一例在使用α干扰素(IFN-α)治疗慢性丙型病毒性肝炎期间发生桥本氏病的病例,该患者具有与甲状腺疾病相关的特定遗传易感性。
一名60岁患有慢性活动性丙型病毒性肝炎(HCV基因型=3a)的女性于1996年11月开始接受IFN-α治疗。治疗前甲状腺功能检查正常,抗甲状腺(抗甲状腺球蛋白和抗甲状腺过氧化物酶)抗体为阴性。在IFN治疗期间,血清转氨酶降至正常范围,病毒血症(血清HCV-RNA)在一年后转为阴性。20个月后,患者出现原发性甲状腺功能减退的临床特征。抗甲状腺抗体呈阳性。激素、超声、放射性碘扫描和细针穿刺检查结果与桥本氏甲状腺炎的诊断一致。患者的组织分型显示存在人类白细胞抗原(HLA)DRB1*11基因(对应于DR5抗原)。暂停IFN-α治疗并开始使用左甲状腺素治疗。IFN-α治疗暂停后慢性病毒感染复发。
本病例报告表明,我们的患者在接受IFN-α治疗慢性丙型肝炎后出现桥本氏病的临床表现与该疾病的特定遗传易感性(DR5)有关。有必要进行进一步研究,以评估对HLA抗原的研究是否可能是检测易发生自身免疫性甲状腺炎患者的非常有用的工具,以便在IFN-α治疗期间早期诊断甲状腺疾病。