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Two Cases of Methimazole-Induced Insulin Autoimmune Syndrome in Graves¡¯ Disease

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³ëÀº ( Roh Eun ) 
Seoul National University College of Medicine Department of Internal Medicine

±è¿¹¾È ( Kim Ye-An ) 
Seoul National University College of Medicine Department of Internal Medicine
±¸À¯Á¤ ( Ku Eu-Jeong ) 
Seoul National University College of Medicine Department of Internal Medicine
¹èÀçÇö ( Bae Jae-Hyun ) 
Seoul National University College of Medicine Department of Internal Medicine
±èÇý¹Ì ( Kim Hye-Mi ) 
Seoul National University College of Medicine Department of Internal Medicine
Á¶¿µ¹Î ( Cho Young-Min ) 
Seoul National University College of Medicine Department of Internal Medicine
¹Ú¿µÁÖ ( Park Young-Joo ) 
Seoul National University College of Medicine Department of Internal Medicine
¹Ú°æ¼ö ( Park Kyong-Soo ) 
Seoul National University College of Medicine Department of Internal Medicine
±è¼º¿¬ ( Kim Seong-Yeon ) 
Seoul National University College of Medicine Department of Internal Medicine
°û¼öÇå ( Kwak Soo-Heon ) 
Seoul National University College of Medicine Department of Internal Medicine

Abstract


We report here the cases of two females with Graves¡¯ disease who developed insulin autoimmune syndrome after treatment with methimazole. The patients exhibited a sudden altered mental state after treatment with methimazole for approximately 4 weeks. Patients had hypoglycemia with serum glucose below 70 mg/dL, and laboratory findings showed both high levels of serum insulin and high titers of insulin autoantibodies. The two women had never been exposed to insulin or oral antidiabetic agents, and there was no evidence of insulinoma in imaging studies. After glucose loading, serum glucose, and total insulin levels increased abnormally. One of the patient was found to have HLA-DRB1*0406, which is known to be strongly associated with methimazole-induced insulin autoimmune syndrome. After discontinuation of methimazole, hypoglycemic events disappeared within 1 month. Insulin autoantibody titer and insulin levels decreased within 5 months and there was no further development of hypoglycemic events. We present these cases with a review of the relevant literature.

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Graves disease;Insulin autoimmune syndrome;Methimazole

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