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.
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.
Objectives:
Current guidelines suggest that patients with cystic fibrosis (CF), who are over the age of 10, should be annually evaluated with oral glucose tolerance test (OGTT). In this study, it was aimed to evaluate the OGTT results in patients above the age of 10, who were followed up in our center with the diagnosis of CF.
Methods:
In the study, 46 patients with CF at the age of 10 and above, who underwent OGTT were included. Data such as gender, age at diagnosis, anthropometric measurements, lung function (FEV1 %) and the OGTT results were obtained. In the analysis, the patient groups with normal glucose tolerance (NGT) and abnormal glucose tolerance(AGT) were compared.
Results:
NGT was found in 37(80.4%) of the patients, and AGT was found in 9(19.5%) of the patients. The median fasting glucose levels of the patients in the NGT group and the mean glucose levels measured at 120 minutes in the OGTT were found to be lower compared to the patients in the AGT group(p<0.005). Although the mean body weight, height, VKİ-SDS, FEV1in the AGT group were found to be lower than the patients in the NGT group, the difference was not statistically significant (p>0.05).
Conclusion:
We detected AGT in approximately 1 out of 5 patients with CF who were at the age of 10 and above. Almost half (44.4%) of the patients with AGT were found to have normal fasting blood glucose levels. Therefore, cystic fibrosis-related diabetes screening should be performed with OGTT instead of fasting blood glucose in patients with CF.
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