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Insulin Autoimmune Syndrome: A Systematic Review
MingXu Lin1, YuHua Chen2,3, Jie Ning1
1Department of Endocrinology, The Affiliated Central Hospital of Shenzhen Longhua District, Guangdong Medical University, Shenzhen 518110, Guangdong, China.
Insulin autoimmune syndrome (IAS) is a rare endocrine disorder causing severe hypoglycemia due to insulin autoantibodies. Early diagnosis and supportive care, including diet and medication, are key for managing this self-limiting condition.
Area of Science:
- Endocrinology
- Immunology
Background:
- Insulin autoimmune syndrome (IAS) is a rare endocrine disorder.
- It is characterized by recurrent severe hypoglycemia, elevated serum insulin, and insulin autoantibodies.
- IAS diagnosis requires excluding other hyperinsulinemic hypoglycemia causes.
Purpose of the Study:
- To provide a comprehensive analysis of IAS.
- To cover epidemiology, pathogenesis, clinical manifestations, diagnosis, and treatment.
- To emphasize the importance of recognizing and managing IAS.
Main Methods:
- Literature review and analysis of IAS cases.
- Discussion of diagnostic criteria, including insulin and C-peptide levels.
- Overview of treatment strategies, from supportive care to immunosuppression.
Main Results:
- IAS diagnosis is confirmed by high insulin autoantibodies with non-parallel C-peptide levels.
- The condition is generally self-limiting with a good prognosis.
- Treatment involves dietary adjustments, glucose absorption modulators, and potentially immunosuppressants or plasma exchange for severe cases.
Conclusions:
- IAS is an important, albeit rare, endocrine disorder requiring clinical attention.
- Accurate diagnosis and tailored management are crucial for patient outcomes.
- Further research can enhance understanding and treatment protocols for IAS.
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