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Trans Abstract

INTRODUCTION

With the ongoing spread of COVID-19 infection, various complications have been reported. Here, we report fulminant type 1 diabetes mellitus (T1DM), which abruptly developed after recovery from COVID-19 infection. The Institutional Review Board (IRB) in Nowon Eulji University Hospital approved our study protocol (IRB No. 18-11-35). Informed consent was obtained from the subject included in the current study.

CASE REPORT

A 41-year-old man with no medical history visited the emergency room for polydipsia and polyuria from 1 week ago. The patient was released from quaran-tine after receiving self-isolation treatment at home after he was tested positive for COVID-19 two weeks ago. For COVID-19, he had only mild myalgia and no fever. The 3 P's symptoms of diabetes developed suddenly and shortly after the symptoms of infection improved. At time of the first visit, his blood pres-sure was 126/72 mm Hg, heart rate was 104 beats per minute, and body temperature was 36.8°C. Physical examination revealed dehydrated tongue, decreased skin turgor and no abdominal tenderness. Height was 174 cm, bodyweight was 70 kg, and body mass index was 23.1 kg/m². The blood tests showed severe hyperglycemia of 721 mg/dL of glucose, elevated lipase (409 IU/L; normal range, 12~53 IU/L), elevated Creactive protein (2.69 mg/dL; normal range, 0~0.3 mg/dL), elevated ketone body with metabolic acidosis (pH 7.18, bicarbonate 9.3 mEq/L). Computed tomography showed no evidence of pancreatitis. And his lipid profile showed no evidence of hypertriglyceridemia (total cholesterol, 234 mg/dL; LDL [low density lipoprotein] cholesterol, 153 mg/dL; triglyceride, 172 mg/dL; and HDL [high density lipoprotein] cholesterol, 62 mg/dL). He was admitted to the intensive care unit with a diagnosis of diabetic ketoacidosis. After intravenous hydration and administration of intravenous insulin, his acidosis improved and glucose level stabilized. He was then transferred to the general ward and started regular diet and subcutaneous multiple insulin injections.

In the blood test confirmed later, glycated hemoglobin (HbA1C) was 6.0% and C-peptide of 0.0 ng/L. Meal-stimulated C-peptide level followed up during his admission period was also 0.0 ng/mL. His glutamic acid decarboxylase (GAD) antibody was elevated (3.3 U/mL; normal range, 0.0~0.9 U/mL) and insulin autoantibody was negative. Those findings fulfilled for the diagnostic criteria of fulminant T1DM. Genetic typing test showed positive for HLA-DRB1*04, HLA-DRB1*12, HLA-DQB1*03, HLA-DQB1*04. After being discharged from the hospital, he is currently under follow-up at the outpatient for 2 months. He is checking his blood glucose with continuous glucose monitoring system and using 50 units of insulin per day as a multiple daily injection without honeymoon period.

DISCUSSION

Fulminant T1DM is one of the subtypes of T1DM, which shows sudden hyperglycemia, absolute insulin deficiency, and near normal HbA1C at the time of first presentation, and negative beta cell autoimmunity at diagnosis is common. In this case, the patient had no history and family history of diabetes, came to the hospital for the first time as diabetic ketoacidosis. HbA1C was 6.0%, which was close to normal. Elevated lipase level suggests that it was accompanied by the destruction of the pancreas without radiologic evidence. He was not an alcohol drinker. He showed complete loss of beta cell function with meal-stimu-lated C-peptide of 0.0 ng/mL. His GAD antibody was positive, and several fulminant T1DM showed positive for GAD antibody and T-cell autoimmunity was shown to be involved in the pathogenesis in fulminant T1DM in previous studies [1,2].

Previous observational study showed HLA-DRB1* 04:05–HLA-DQB1*04:01 haplotype was significantly associated with increased risk of fulminant T1DM in Korean population [3]. His genetic typing showed positive for HLA-DRB1*04, HLA-DRB1*12, HLA-DQB1*03, HLA-DQB1*04. It can be assumed that susceptible genotype and combined autoimmunity evoked irreversible beta cell destruction and fulminant T1DM, although futher investigations are required to find more evidence.

In vitro study showed pancreas islet beta cells can be infected by COVID-19 virus. It is known that this can lead to islet cell dysfunction and may trigger beta cell autoimmunity [4,5]. Indeed, several previous studies reported that COVID-19 increased new-onset T1DM in European pediatric populations [6,7]. In this case, it is meaningful in that fulminant T1DM with a clear temporal precedence after COVID-19 infection. Fulminant T1DM is rarely reported outside of Asia. There are one case report from China that Fulminant T1DM developed soon after COVID-19 vaccination [8]. To our knowledge, this is the first case of fulminant T1DM that occurred after COVID-19 infection, here we report this case.

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