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Galectin-3 levels in children with cystic fibrosis
Dilber Ademhan Tural1, Nagehan Emiralioglu2, Senay Akin3
1Department of Pediatric Pulmonology, Ankara Bilkent City Hospital, Ankara, Turkey. dilberademhan@gmail.com.
Insights
Children with cystic fibrosis (CF) show elevated serum Galectin-3 levels compared to healthy children. This biomarker
Area of Science:
- Biochemistry
- Immunology
- Pediatrics
Background:
- Galectin-3 is implicated in chronic inflammation and fibrosis across various organs.
- Cystic fibrosis (CF) lung disease is characterized by obstruction, infection, and inflammation.
- Galectin-3 is emerging as a potential biomarker in inflammatory and fibrotic conditions.
Purpose of the Study:
- To investigate the role of serum Galectin-3 in pediatric patients with cystic fibrosis.
- To compare Galectin-3 concentrations in CF patients with healthy controls.
- To explore correlations between Galectin-3 levels and clinical parameters in CF.
Main Methods:
- A cross-sectional, case-control study involving 143 CF patients and 30 healthy children.
- Measurement of serum and sputum Galectin-3, IL-17A, IL-8, and neutrophil elastase (NE) using ELISA.
- Statistical analysis to compare groups and assess correlations with age, BMI, and lung function.
Main Results:
- Serum Galectin-3 and NE concentrations were significantly higher in CF patients than in controls.
- Serum Galectin-3 levels correlated positively with age and body mass index (BMI) in CF children.
- Sputum Galectin-3 showed a negative correlation with lung function parameters like FEV1 and FVC.
Conclusions:
- Children with CF exhibit increased serum Galectin-3 levels, suggesting its involvement in the disease.
- Serum Galectin-3 levels in CF patients are influenced by age, gender, and BMI.
- Sputum Galectin-3 levels correlate with reduced lung function in cystic fibrosis.
Abstract:
Cystic fibrosis (CF) is a multisystemic disease in which airway obstruction, infection, and inflammation play a critical role in the pathogenesis and progression of CF lung disease. The carbohydrate-binding protein Galectin-3 is increased in several inflammatory and fibrotic diseases and has recently been forwarded as a biomarker in these diseases. We aimed to define the role of serum Galectin-3 in children with CF by comparison with healthy subjects. This is a cross-sectional, case-control study. 143 CF and 30 healthy subjects were enrolled in the study. Peripheral blood and sputum concentrations of Galectins-3, interleukin (IL)-17A, IL-8, and neutrophil elastase (NE) were determined with commercial ELISA kits. There was no significant difference between the groups in age and gender (p = 0.592, p = 0.613, respectively). Serum Galectin-3 and NE concentrations were higher in the patient group than in healthy controls (p = 0.002, p < 0.001, respectively). There were no significant differences between groups according to IL-17A and IL-8 concentrations. Serum Galectin-3 was correlated with age (r = 0.289, p < 0.001) and body mass index (BMI) (r = 0.493, p < 0.001) in children with CF. Sputum Galectin-3 levels are negatively correlated with percent predictive forced expiratory volume in 1 s (FEV1) (r = - 0.297, p = 0.029), FEV1 z-score, (r = - 0.316, p = 0.020), percent predictive forced vital capacity (FVC) (r = - 0.347, p = 0.010), and FVC z-score (r = - 0.373, p = 0.006). Conclusion: The study shows that serum Galectin-3 levels increased in clinically stable CF patients, and serum Galectin-3 response may depend on age, gender, and BMI. The sputum Galectin-3 was found to be negatively correlated with patients' lung functions. What is known: • Galectin-3 is a key regulator of chronic inflammation in the lung, liver, kidney, and tumor microenvironment. What is new: • Children with cystic fibrosis (CF) have higher serum Galectin-3 concentrations than healthy children. • Serum Galectin-3 expression influenced by age, BMI, and gender in children with CF.
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