AI Article Synopsis

  • Transient neonatal diabetes mellitus (TNDM) is a rare condition causing diabetes in infants that typically resolves by 18 months but may relapse around 14 years of age, often with complications like hyperinsulinaemia.
  • A case study examined a patient with TNDM due to a genetic anomaly, tracking their glycaemic profiles and insulin function from remission to relapse, revealing initially impaired insulin response but gradually improving fasting insulin levels.
  • Overall, the study provided the first detailed report on the changes in β-cell function and insulin resistance during the remission phase of TNDM, indicating significant fluctuations over time.

Article Abstract

Introduction: Transient neonatal diabetes mellitus (TNDM) is a rare condition that is characterized by the presence of diabetes mellitus during the first 6 months of life and remission by 18 months of age. It usually relapses at a median age of 14 years. Hyperinsulinaemic hypoglycaemia is a relatively common complication during remission. Although β-cell function is reported to be impaired at relapse, the clinical course of glycaemic profiles during remission in patients with TNDM remains largely unknown.

Case Presentation: Longitudinal glycaemic profiles were investigated annually from remission (185 days) to relapse (14.5 years) in a patient with TNDM due to paternal 6q24 duplication using the oral glucose tolerance test (glucose intake: 1.75 g/kg to a maximum of 75 g). The patient's β-cell function and insulin sensitivity were assessed by calculating the insulinogenic index, homeostasis model assessment of β-cell function (HOMA-β), homeostasis model assessment of insulin resistance (HOMA-IR), quantitative insulin sensitivity check index, and Matsuda index. Early insulin response to glucose intake was impaired throughout remission, whereas fasting insulin and β-cell function by HOMA-β gradually increased in the first few years since remission, followed by a gradual decline in function. In contrast, HOMA-IR fluctuated and peaked at 6.5 years of age.

Conclusion: This is the first report of annual longitudinal glycaemic profiles in a patient with 6q24-related TNDM during remission. We identified fluctuations in β-cell function and insulin resistance during remission.

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Source
http://dx.doi.org/10.1159/000518617DOI Listing

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