Case report
The patient, who was male and 27-years-old, was referred to the People's Hospital of Jizhou District (Tianjin, China), due to palpitation, fatigue, fear of heat, sweating and weight loss of 10 kg within 3 months. The thyroid function test results are presented in Table I. The patient was diagnosed with hyperthyroidism and treated with methimazole (10 mg, 3 times daily). After 10 days of continuous methimazole administration, the patient had aggravated symptoms and developed paralysis of the limbs and labored breathing, with a blood potassium level of 1.91 mmol/l (normal range, 3.5-5.3 mmol/l). Following symptomatic treatment, which included intravenous and oral potassium supplementation, the patient improved, and was subsequently treated with intermittent potassium supplementation.
However, the patient still had intermittent fatigue and palpitations and was subsequently admitted to Tianjin First Center Hospital (Tianjin, China). The patients thyroid was diffusely enlarged on palpation and there was no exophthalmos. The cardiac and respiratory examination findings were unremarkable. The abdomen was soft and non-tender, without masses. The examination results of the thyroid function test performed following admission are also presented in Table I. The erythrocyte sedimentation rate was normal, while the thyroid color doppler ultrasound indicated that the thyroid gland double-lobe gland was enlarged, and blood flow was normal. The patient was diagnosed with Graves' disease and continued to be treated with methimazole (10 mg, twice daily). Following treatment with potassium supplementation, the fluctuation in the blood potassium level was monitored at 3.17-4.67 mmol/l (normal range, 3.5-5.3 mmol/l); however, the symptoms, such as fatigue, palpitation and hand tremors, appeared intermittently. By monitoring the finger blood glucose level, it was demonstrated that the minimum finger blood glucose level was 1.90 mmol/l, and the plasma blood glucose level was 2.44 mmol/l. Therefore, a spontaneous hypoglycemia episode was identified. The patient had no history of diabetes mellitus or hypoglycemia and denied exposure to insulin or oral antidiabetic drugs. The glycosylated hemoglobin level was 6.0% (normal range, 4.0-6.0%). The patient had an oral glucose tolerance test (OGTT), insulin release test and C-peptide release test (Fig. 1). The time intervals of these tests were 0, 30, 60, 120 and 180 min. All results of the insulin release test were >1,000 µIU/ml. IAA was positive, while tests for glutamic acid decarboxylase antibody and islet cell antibody were negative. There were no abnormalities in routine blood, blood biochemistry, rheumatism immunity series, anti-nuclear antibody spectrum and adrenal function tests. A pancreatic CT and enhanced CT did not reveal any abnormalities. Using the Naranjo's assessment scale (7), the causal association had a score of 7 points (Table II). Considering hypoglycemia may be secondary to methimazole-induced IAS, methimazole was discontinued. The patient did not experience hypoglycemia again, once his eating habits were changed, he had more meals a day but with a reduction in the amount consumed. The patient was ingesting food higher in protein and fiber to delay gastric emptying and a slowdown in the insulin release rate. The examination before discharge indicated that the fasting serum insulin level (634.0 µIU/ml), was significantly lower than before treatment. After 2 weeks, the patient was treated with I-131 11 mCi. Outside of the hospital, using blood glucose monitoring, a hypoglycemia episode did not occur. Furthermore, the insulin level of the patient was lower, as presented in Fig. 2. The fasting blood glucose and insulin were recorded on days 0, 9, 17, 31 and 79. The results of the OGTT, insulin and C-peptide tests are presented in Fig. 3 and were obtained >2 months after discharge. The time intervals of these tests were 0, 30, 60, 120 and 180 min. The insulin and C-peptide levels had decreased markedly compared to those on admission, and no hypoglycemia occurred.
Discussion
The patient in the present case report presented with hypokalemia and hypoglycemia following treatment for hyperthyroidism with methimazole. Hypoglycemia may be easily missed at diagnosis or misdiagnosed (5). Following treatment with potassium supplementation, the patient experienced symptoms, such as fatigue, palpitation and hand tremors, which occurred intermittently. By monitoring finger blood glucose levels, spontaneous hypoglycemia episodes were identified. The patient had no history of diabetes mellitus and hypoglycemia, or exposure to insulin or oral antidiabetic agents. Therefore, hypoglycemia caused by oral hypoglycemic drugs or exogenous insulin was excluded. The insulin and C-peptide release test revealed that levels of insulin were elevated, and although the C-peptide level was high, it was not synchronized with the insulin level. IAA was indicated to be positive, and no pancreatic abnormalities were identified following a pancreatic CT. The patient discontinued with methimazole treatment. Using dietary management, hypoglycemia did not return. Therefore, hypoglycemia was indicated to be caused by IAS. IAS is a typical clinical symptom of recurrent, spontaneous and severe hypoglycemia induced by non-exogenous insulin in the blood and requires the identification of insulinoma. However, pancreatic space-occupying lesions are often observed in the CT images of patients with insulinoma, although some small insulinomas are difficult to locate. The elevated serum insulin level in these patients are synchronous with C-peptide, and IAA is negative. The plasma C-peptide levels in patients with IAS have also been indicated to be elevated, but it is much lower compared with the insulin concentration in the blood, showing a state of separation of C-peptide from insulin (8). IAA has a high titer; therefore, detection of IAA, serum insulin and C-peptide levels can assist with identification of this disorder (9).
Using the Naranjo's assessment scale (7), the causal association had a score of 7 points (Table II), which supported the possible causal relationship between the use of methimazole and IAS. The pathogenesis of IAS is still unclear and it is currently hypothesized to develop from the combined action of autoimmune defects and IAA induced by the administration of specific drugs, on the basis of susceptibility genes (4,6). Using sulfur/sulfhydryl-containing drugs is an important treatment method, and these include methimazole, captopril, D-penicillamine, hydralazine, glutathione, methionine, mercaptans, imipenem, penicillin G, α-lipoic acid and diltiazem (10). Any one of these can induce IAS, and methimazole is the most common treatment option (11). It has been debated that sulfur/sulfhydryl groups may be able to bind and reduce the sulfhydryl bonds connecting insulin chains A and B, making endogenous insulin more immunogenic (12). Studies have demonstrated that IAA in patients with IAS is characterized by low affinity and high capacity (4,13). IAA can also form an unstable complex with insulin, reduce the concentration of serum-free insulin, expand insulin storage capacity, and further stimulate islet B cells to continue to secrete insulin. When the insulin-IAA complex dissociates, a large amount of free insulin is released into the blood to cause hyperinsulinemia, which in turn causes hypoglycemia (14). The patient in the present case report had a history of methimazole exposure, which supports an etiological role for drugs with sulfhydryl groups in the development of IAS.
From 2001 to September 2019, 64 cases of IAS induced by methimazole were identified in the Chinese Biomedical Literature Database (https://www.cnki.net/) and the patient characteristics are presented in Table III. Among them, 16 patients were males and 48 were females, 6 were >60-years-old and 58 were <60-years-old. The reason for the increased amount of women diagnosed may be that the incidence of hyperthyroidism in women is significantly higher than in men, and the incidence of hyperthyroidism in young people is higher than in people of old age. Patients with hyperthyroidism may also have hypokalemia, and 2 out of 64 patients also had hypokalemia. The patient in the present case report had Graves' disease with intermittent hypokalemia and periodic paralysis, which is more common in young males. Hypoglycemia occurs irregularly, and can manifest as hypoglycemia at night or early in the morning and as reactive hypoglycemia following the ingestion of food (5,6). The degree of hypoglycemia in the cases was indicated to be different, with 60 cases having blood glucose levels >2.8 mmol/l and 4 cases with levels >2.8 mmol/l. The hypoglycemia episode patient described in the present case report was also irregular, and his lowest fingertip blood glucose level was 1.90 mmol/l. A previous study (10) have indicated that the treatment of IAS first requires eliminating the inducement, discontinuing the causative drugs, dietary management, delaying gastric emptying by increasing the number of meals a day with a reduction in the amount and ingestion of high protein and high fiber food and slowing the release rate of insulin. α-Glucosidase inhibitors have also been used to reduce or prevent hypoglycemic episodes (4,13). In more severe or prolonged cases, glucocorticoids, immunosuppressants and plasmapheresis may be beneficial adjuvant therapies (15,16). Of the 64 cases, 21 patients adjusted their diet, 38 patients were treated with combined glucocorticoid therapy, 2 patients were treated with combined α-glucosidase inhibitors and 3 patients were treated with glucocorticosteroids and α-glucosidase inhibitors to treat hypoglycemia. In the patient described in the present case report, there was no recurrence of hypoglycemia following diet management and the discontinuation of methimazole. When Graves' disease is combined with IAS, treatment with I-131 is often advocated (17). Of the 64 patients, 25 were treated with I-131, 19 were treated with propylthiouracil (PTU), 4 were switched to I-131 therapy following oral PTU treatment, 2 cases received surgical treatment and 14 cases were previously treated with methimazole only or it was not explicitly stated. Patients with hyperthyroidism receiving methimazole treatment may also develop IAS; however, not all the patients had Graves' disease. The patient in the present case report stopped methimazole treatment and was instead treated with radioactive iodine for Graves' disease. In previous studies (18,19) it has been hypothesized that HLA-DR4 is a genetic susceptibility gene for IAS and is associated with the pathogenesis of IAS. In addition, studies have demonstrated that 84% of patients from Japan carry the HLA-DRB1*0406 allele (20), while European and American populations primarily carry the HLA-DRB1*0403 allele (21,22). Unfortunately, the patient in the current case report did not undergo genetic testing. Of the 64 patients previously reported, 3 were genetically tested (23), and all the patients were indicated to carry the HLA-DRB1*0406 allele, which is consistent with the reported results of previous Asian populations.
The patient in the present case report exhibited IAS. The patient was also previously diagnosed with Graves' disease and suffered with intermittent hypokalemic periodic paralysis. Hypoglycemia might be easily missed in diagnosis or misdiagnosed. Monitoring fingertip blood glucose level is a convenient and feasible method to determine this. The majority of patients with IAS exhibit a good prognosis. However, it is a rare cause of hypoglycemia in clinical practice, and it is susceptible to misdiagnosis and missed diagnosis. This may lead to severe adverse effects, such as severe hypoglycemia and even disturbance of consciousness. For patients that also exhibit autoimmune diseases, who have used or are using suspicious drugs and are developing spontaneous hypoglycemia, insulin levels and IAA should be monitored in time. Therefore, early diagnosis and appropriate treatment should be conducted to reduce adverse consequences for patients with IAS.