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.

PubMed

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.

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