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Association of Islet Amyloid Polypeptide to C-Peptide Ratio With Cystic Fibrosis-Related Diabetes: A Prospective
Insights
The islet amyloid polypeptide (IAPP) to C-peptide ratio is a potential biomarker for early detection of cystic fibrosis (CF) related diabetes (CFRD). This ratio was significantly higher in CFRD patients, aiding in CFRD diagnosis.
Area of Science:
- Endocrinology
- Metabolic Disorders
- Pulmonology
Background:
- Early detection of cystic fibrosis (CF) related diabetes (CFRD) is crucial for improving patient outcomes and reducing mortality.
- Identifying reliable biomarkers for CFRD is essential for timely diagnosis and management.
Purpose of the Study:
- To evaluate the diagnostic potential of the islet amyloid polypeptide (IAPP) to C-peptide ratio in distinguishing between CF patients with and without CFRD.
- To investigate the association of the IAPP:C-peptide ratio with key clinical parameters in CF patients.
Main Methods:
- A cross-sectional analysis was performed on a prospective cohort of 33 participants, including individuals with CF and CFRD.
- Plasma IAPP:C-peptide ratios were measured and correlated with glycated hemoglobin and lung function markers.
Main Results:
- The median IAPP:C-peptide ratio was significantly higher in patients with CFRD compared to those without (P = 0.004).
- The IAPP:C-peptide ratio explained 38% of the variation in diabetes status among CF patients (r2 = 0.399, P < 0.001).
- IAPP levels showed a strong correlation with serum ferritin and forced expiratory volume in CFRD patients.
Conclusions:
- The IAPP:C-peptide ratio shows promise as a potential biomarker for CFRD in adults with CF.
- Further validation in longitudinal studies is necessary to confirm the predictive capability of the IAPP:C-peptide ratio for CFRD.
Objectives:
Early detection of cystic fibrosis (CF) related diabetes (CFRD) improves health outcomes and reduces CF-related mortality. The study aims to evaluate the ratio of islet amyloid polypeptide (IAPP) to C-peptide in CF patients with diabetes and without diabetes.
Methods:
Cross-sectional analysis was carried out in a prospective cohort of 33 participants (CF [n = 16] and CFRD [n = 18]). We examined the association of plasma IAPP:C-peptide ratio with clinical information, including glycated hemoglobin, and lung function markers.
Results:
The median (interquartile range) IAPP:C-peptide ratio was significantly (P = 0.004) higher in people with CFRD (4.8 [4.5]) compared with participants without CFRD (12.1 [19.7]). The ratio of IAPP to C-peptide significantly accounted for a 38% variation in the diabetes status in patients with CF (r2 = 0.399, P < 0.001). Islet amyloid polypeptide is strongly correlated with serum ferritin levels (r = 0.683, P = 0.005) and forced expiratory volume in CFRD, but not in nondiabetic participants with CF.
Conclusions:
Islet amyloid polypeptide:C-peptide ratio could be a potential marker of CFRD in adults with CF. Further research requires validation of this marker in longitudinal cohort studies to confirm the capability of IAPP:C-peptide to predict CFRD.
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