Related Experiment Video
Updated: Jun 25, 2025

Detection and Quantification of Calcitonin Gene-Related Peptide CGRP in Human Plasma Using a Modified Enzyme-Linked Immunosorbent Assay
Published on: June 16, 2023
Calcitonin Gene-Related Peptide Level in Cystic Fibrosis Patients
Sabina Galiniak1, Marek Biesiadecki1, Iwona Rościszewska-Żukowska1
1Institute of Medical Sciences, Medical College, Rzeszów University, Warzywna 1a, 35-310 Rzeszów, Poland.
Serum levels of alpha calcitonin gene-related peptide (αCGRP) are significantly elevated in cystic fibrosis (CF) patients compared to healthy individuals. This finding suggests a potential role for αCGRP in CF pathophysiology.
Area of Science:
- Respiratory Medicine
- Neuropeptide Research
- Genetic Disorders
Background:
- Calcitonin gene-related peptide (CGRP) is involved in respiratory tract physiology and pathophysiology.
- Limited data exist on the role of CGRP in cystic fibrosis (CF).
Purpose of the Study:
- To determine serum alpha CGRP (αCGRP) concentrations in patients with CF.
- To investigate the relationship between αCGRP levels and CFTR mutation types and disease severity.
Main Methods:
- Serum αCGRP levels were measured using enzyme-linked immunosorbent assay.
- 64 CF patients and 31 healthy controls were included.
- CF patients were analyzed based on CFTR mutation type and spirometry results.
Main Results:
- CF patients exhibited significantly higher serum αCGRP levels (62.51 ± 15.45 pg/mL) than controls (47.43 ± 8.06 pg/mL).
- Homozygotes for the ΔF508 mutation had higher αCGRP levels than heterozygotes.
- αCGRP levels were higher in patients with severe CF compared to mild CF.
Conclusions:
- Serum αCGRP is significantly elevated in CF patients.
- Increased αCGRP may play a role in CF pathophysiology.
- Further research is warranted to explore αCGRP's function in CF.
Related Concept Videos
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
Cystic Fibrosis: Management
Sinus disease and chronic...
Synthesis and Functions of Calcitonin
The exact mechanisms by which calcitonin operates in calcium homeostasis remain elusive, but its significance is evident in several vital...
Cell Specific Gene Expression

