Abstract

BackgroundThe exact incidence, clinical features and uniform diagnostic criteria of exogenous insulin autoimmune syndrome (EIAS) are still unclear. The purpose of this study is to explore the clinical characteristics of EIAS and to provide a structural approach for clinical diagnosis, treatment and prevention.MethodsThe literature on EIAS in Chinese and English from 1970 to 2020 was collected for retrospective analysis.ResultsA total of 122 patients (33 males and 73 females) were included in the study with a median age of 67 years (range 14–86) and a median HbA1c of 7.7%. EIAS mainly occurred in type 2 diabetes mellitus patients using premixed insulin. Symptoms manifested were hypoglycemia in 86.54%, recurrent episodes of symptomatic hypoglycemia in 35.58%, nocturnal hypoglycemia along with daytime hyperglycemia in 21.15% and recurrent hypoglycemia after discontinued insulin in 64.43%. The onset of symptoms occurred at night, in the early morning or during fasting, ranging from a few days to 78 months after the administration of insulin. The mean blood glucose level during the hypoglycemic phase was 2.21 mmol/L (range 1–3.4), and the serum insulin levels were mainly ≥ 100 U/mL and were associated with low C-peptide levels (≤ 10 ng/ml). Insulin autoantibodies (IAAs) were positive in all EIAS patients. The 75-g extended oral glucose tolerance test (OGTT) mainly showed a diabetic curve. Pancreatic imaging was unremarkable. Withdrawal of insulin alone or combination of oral hypoglycemic agents or replacement of insulin formulations or with corticosteroid treatment eliminated hypoglycemia in a few days to 3 months. IAA turned negative in 6 months (median, range 1–12). No hypoglycemia episodes were observed at a median follow-up of 6 months (range 0.5–60).ConclusionsEIAS is an autoimmune disease caused by insulin-binding antibodies in susceptible subjects. Insulin antibodies change glucose dynamics and could increase the incidence of hypoglycemic episodes. Detection of insulin antibodies is the diagnostic test. Changing therapeutic modalities reduced the incidence of hypoglycemic episodes.

Highlights

  • The exact incidence, clinical features and uniform diagnostic criteria of exogenous insulin autoimmune syndrome (EIAS) are still unclear

  • We identified the literature regarding insulin antibody syndrome induced by exogenous insulin using the search terms “insulin antibody syndrome”, “exogenous insulin”, “autoimmune hypoglycemia”, “hypoglycemia” and “Hirata disease”

  • Among the patients reported in the literature, 119 patients (97.54%) were from Asia, 100 patients (90.91%) had type 2 diabetes mellitus (T2DM), and 6 patients (5.45%) had type 1 diabetes mellitus (T1DM)

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Summary

Introduction

The exact incidence, clinical features and uniform diagnostic criteria of exogenous insulin autoimmune syndrome (EIAS) are still unclear. IAS can be spontaneous or triggered by exposure to viruses or drugs [3]. Hypoglycemia induced by exogenous insulin in diabetic patients has shown symptoms similar to IAS. Some scholars named it exogenous insulin autoimmune syndrome (EIAS) as a nonclassic IAS [5]. The exact incidence, clinical features and uniform diagnostic criteria of EIAS are still unclear. The evidence of IAS induced by exogenous insulin treatment is limited to case reports. We collected patients with exogenous insulin-induced autoimmune hypoglycemia to summarize the clinical features, diagnostic tests, treatment and prevention

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