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首页> 外文期刊>European journal of gastroenterology and hepatology >Development of insulin-dependent diabetes mellitus in a patient with chronic hepatitis C during therapy with interferon-alpha.
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Development of insulin-dependent diabetes mellitus in a patient with chronic hepatitis C during therapy with interferon-alpha.

机译:慢性丙型肝炎患者用干扰素-α治疗期间胰岛素依赖型糖尿病的发展。

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Interferon (IFN)-alpha is used for the treatment of chronic viral hepatitis. It has been associated with various forms of autoimmune disease, e.g. autoimmune hepatitis, Hashimoto thyroiditis and insulin-dependent diabetes mellitus. Further, an increase of insulin resistance and development of non-insulin-dependent diabetes mellitus has been described after treatment with IFN-alpha. Several studies have investigated the induction of different autoimmune markers by IFN-alpha, but only few specified patients who developed insulin-dependent diabetes mellitus. We report the case of a 37-year-old man with chronic hepatitis C who was treated with IFN-alpha plus ribavirin. Thirty weeks after the start of treatment, the patient developed insulin-dependent diabetes mellitus and therapy was withdrawn. HLA typing showed an HLA-DR1,3 phenotype. At manifestation of diabetes mellitus, the C-peptide level was 0.37 ng/ml (normal range 0.5-3 ng/ml). The patient had a positive family history for type 2 diabetes. Several autoimmune markers were investigated before, during and 6 months after withdrawal of antiviral treatment. High titres of glutamic acid decarboxylase (GAD) antibodies were present before therapy. A significant increase in titres of islet cell antibodies, parietal cell antibodies and sperm antibodies was present after 14 weeks of IFN-alpha treatment. Six months after withdrawal of IFN-alpha therapy, these antibodies had significantly decreased whereas GAD antibodies remained unchanged. There was no clinical sign of any other autoimmune disease. Our data show that, in patients with a predisposition to insulin-dependent diabetes mellitus, the disease may become manifest as a side-effect during therapy with IFN-alpha. Several pathogenetic factors may be involved in this process, and, in addition to IFN-alpha, hepatitis C itself may induce autoimmune mechanisms. We conclude that screening for autoantibodies specific for type 1 diabetes should be performed before the start of IFN-alpha treatment. In patients found to be at increased risk of developing diabetes mellitus type 1, monitoring of titres of these antibodies during therapy could help to assess the individual risk-benefit ratio of IFN-alpha treatment.
机译:干扰素(IFN)-α用于治疗慢性病毒性肝炎。它已与多种形式的自身免疫性疾病相关,例如自身免疫性肝炎,桥本甲状腺炎和胰岛素依赖型糖尿病。此外,已经描述了在用IFN-α治疗后胰岛素抵抗的增加和非胰岛素依赖性糖尿病的发展。几项研究调查了IFN-α对不同自身免疫标记的诱导作用,但只有少数特定患者出现了胰岛素依赖型糖尿病。我们报告了一例37岁的慢性丙型肝炎患者,接受IFN-α加利巴韦林治疗。开始治疗后三十周,患者发展出胰岛素依赖型糖尿病,并退出治疗。 HLA分型显示出HLA-DR1,3表型。在糖尿病表现时,C肽水平为0.37 ng / ml(正常范围为0.5-3 ng / ml)。该患者有2型糖尿病的阳性家族史。在停止抗病毒治疗之前,期间和之后的6个月,研究了几种自身免疫标记。治疗前存在高滴度的谷氨酸脱羧酶(GAD)抗体。 IFN-α治疗14周后,胰岛细胞抗体,壁细胞抗体和精子抗体的滴度显着增加。停用IFN-α治疗后六个月,这些抗体显着下降,而GAD抗体保持不变。没有任何其他自身免疫性疾病的临床体征。我们的数据显示,在易患胰岛素依赖型糖尿病的患者中,该疾病可能在用IFN-α进行治疗期间表现为副作用。此过程可能涉及多种致病因素,除了IFN-α之外,丙型肝炎本身也可能诱导自身免疫机制。我们得出的结论是,应在开始进行IFN-α治疗之前筛查针对1型糖尿病的特异性自身抗体。在发现罹患1型糖尿病的风险增加的患者中,在治疗期间监测这些抗体的滴度可以帮助评估IFN-α治疗的个体风险获益比。

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