Evaluation of Oral Glucose Tolerance Test Results in Children with Cystic Fibrosis

Asli Bestas1, Edip Unal1, Amine Aktar Karakaya1

  • 1Department of Pediatric Endocrinology, Dicle University Faculty of Medicine, Diyarbakir, Türkiye.

Sisli Etfal Hastanesi Tip Bulteni
|October 16, 2024
PubMed

Insights

Approximately 1 in 5 cystic fibrosis patients over 10 years old have abnormal glucose tolerance. Oral glucose tolerance tests (OGTT) are recommended over fasting blood glucose for screening CF-related diabetes.

Area of Science:

  • Endocrinology
  • Pulmonology
  • Metabolic Disorders

Background:

  • Current guidelines recommend annual oral glucose tolerance tests (OGTT) for cystic fibrosis (CF) patients over 10.
  • Early detection of glucose metabolism abnormalities is crucial in CF management.

Purpose of the Study:

  • To evaluate OGTT results in CF patients aged 10 and above.
  • To determine the prevalence of abnormal glucose tolerance (AGT) in this population.
  • To compare screening methods for cystic fibrosis-related diabetes.

Main Methods:

  • 46 CF patients aged 10+ underwent OGTT.
  • Data collected included demographics, anthropometrics, lung function (FEV1%), and OGTT results.
  • Patients were categorized into normal glucose tolerance (NGT) and AGT groups for comparison.

Main Results:

  • AGT was detected in 19.5% of patients.
  • Patients with AGT had higher median fasting glucose and mean 120-minute OGTT glucose levels compared to NGT patients (p<0.005).
  • Lower anthropometric and lung function parameters were observed in the AGT group, though not statistically significant.

Conclusions:

  • AGT affects approximately 1 in 5 older CF patients.
  • Nearly half of patients with AGT had normal fasting glucose, highlighting limitations of fasting glucose screening.
  • OGTT is a more effective screening tool for cystic fibrosis-related diabetes than fasting blood glucose in patients aged 10 and above.
Abstract

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