Covelli Danila, Vannucchi Guia, Campi Irene, Currò Nicola, D'Ambrosio Roberta, Maggioni Marco, Gianelli Umberto, Beck-Peccoz Paolo, Salvi Mario
Graves' Orbitopathy Center, Endocrine Unit (D.C., G.V., I.C., P.B.-P., M.S.), Ophthalmology (N.C.), Department of Gastroenterology and Hepatology (R.D.), Pathology Unit, and Department of Pathophysiology and Transplantation (M.M., U.G.), Fondazione Ca' Granda IRCCS, Ospedale Maggiore Policlinico and University of Milan, 20122 Milan, Italy.
J Clin Endocrinol Metab. 2015 May;100(5):1731-7. doi: 10.1210/jc.2014-4463. Epub 2015 Mar 9.
Intravenous glucocorticoids (IVGC) administered at high doses for the treatment of active moderate-severe Graves' orbitopathy (GO) may induce liver toxicity. Cumulative doses should not exceed 8 g and strict monitoring of liver function is recommended to avoid potentially life-threatening side effects. The 3-hydroxy-3-methylglutaryl-coenzyme reductase inhibitors, also known as statins, are employed to prevent major cardiovascular events. Patients with active GO, requiring immunosuppression with IVGC, are often treated with statins also.
We studied a 64-year-old man and a 58-year-old woman who developed significant liver toxicity after moderate doses of IVGC (methylprednisolone 2.3 g and 5 g in patients 1 and 2, respectively) and concomitant administration of statins.
Liver function tests were monitored every two weeks. Hepatitis virus markers and serology for autoimmune hepatitis were negative. At the occurrence of liver dysfunction (5-fold increase of serum aspartate aminotransferase/alanine aminotransferase concentrations), in patient 1 we stopped simvastatin indefinitely and discontinued IVGC for 2 weeks, whereas in patient 2, ongoing treatment with rosuvastatin was discontinued 3 weeks after IVGC therapy.
In patient 1, off simvastatin, liver function remained normal after resuming IVGC. In patient 2, a further increase of the aminotransferase values was observed 3 weeks after IVGC discontinuation, with a progressive normalization only after statin withdrawal.
Our study shows that statins, when concomitantly employed with methylprednisolone, may be a cause of liver dysfunction during IVGC in active GO. An accurate pharmacological history of all patients who are candidates for IVGC treatment is suggested to identify subjects at risk for hepatotoxicity.
高剂量静脉注射糖皮质激素(IVGC)用于治疗活动性中重度格雷夫斯眼眶病(GO)时可能会诱发肝毒性。累积剂量不应超过8 g,建议严格监测肝功能以避免潜在的危及生命的副作用。3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂,即他汀类药物,用于预防重大心血管事件。需要用IVGC进行免疫抑制治疗的活动性GO患者通常也会使用他汀类药物。
我们研究了一名64岁男性和一名58岁女性,他们在接受中等剂量的IVGC(患者1和患者2分别为2.3 g和5 g甲泼尼龙)并同时服用他汀类药物后出现了严重的肝毒性。
每两周监测一次肝功能。肝炎病毒标志物和自身免疫性肝炎血清学检查均为阴性。在出现肝功能障碍(血清天冬氨酸氨基转移酶/丙氨酸氨基转移酶浓度升高5倍)时,患者1无限期停用辛伐他汀,并停用IVGC 2周,而在患者2中,瑞舒伐他汀的持续治疗在IVGC治疗3周后停药。
在患者1中,停用辛伐他汀后,恢复IVGC治疗后肝功能仍保持正常。在患者2中,停用IVGC 3周后观察到转氨酶值进一步升高,仅在停用他汀类药物后才逐渐恢复正常。
我们的研究表明,在活动性GO患者接受IVGC治疗期间,他汀类药物与甲泼尼龙同时使用可能是肝功能障碍的一个原因。建议对所有接受IVGC治疗的患者进行准确的用药史记录,以识别有肝毒性风险的患者。