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Galectin-3 levels in children with cystic fibrosis.
Ademhan Tural, Dilber; Emiralioglu, Nagehan; Akin, Senay; Alboga, Didem; Ozsezen, Beste; Nayir Buyuksahin, Halime; Guzelkas, Ismail; Kasikci, Merve; Sunman, Birce; Gungor, Irem; Yalcin, Ebru; Dogru, Deniz; Kiper, Nural; Demirel, Ali Haydar; Ozcelik, Ugur.
Afiliação
  • Ademhan Tural D; Department of Pediatric Pulmonology, Ankara Bilkent City Hospital, Ankara, Turkey. dilberademhan@gmail.com.
  • Emiralioglu N; Department of Pediatric Pulmonology, School of Medicine, Hacettepe University, Ihsan Dogramaci Children's Hospital, Ankara, Turkey.
  • Akin S; Faculty of Sport Sciences, Department of Exercise and Sport Sciences, Exercise, and Sport Physiology Division, Hacettepe University, Ankara, Turkey.
  • Alboga D; Department of Pediatric Pulmonology, School of Medicine, Hacettepe University, Ihsan Dogramaci Children's Hospital, Ankara, Turkey.
  • Ozsezen B; Department of Pediatric Pulmonology, School of Medicine, Hacettepe University, Ihsan Dogramaci Children's Hospital, Ankara, Turkey.
  • Nayir Buyuksahin H; Department of Pediatric Pulmonology, School of Medicine, Hacettepe University, Ihsan Dogramaci Children's Hospital, Ankara, Turkey.
  • Guzelkas I; Department of Pediatric Pulmonology, School of Medicine, Hacettepe University, Ihsan Dogramaci Children's Hospital, Ankara, Turkey.
  • Kasikci M; Department of Biostatistics, Hacettepe University, Ankara, Turkey.
  • Sunman B; Department of Pediatric Pulmonology, School of Medicine, Hacettepe University, Ihsan Dogramaci Children's Hospital, Ankara, Turkey.
  • Gungor I; Faculty of Sport Sciences, Department of Exercise and Sport Sciences, Exercise, and Sport Physiology Division, Hacettepe University, Ankara, Turkey.
  • Yalcin E; Department of Pediatric Pulmonology, School of Medicine, Hacettepe University, Ihsan Dogramaci Children's Hospital, Ankara, Turkey.
  • Dogru D; Department of Pediatric Pulmonology, School of Medicine, Hacettepe University, Ihsan Dogramaci Children's Hospital, Ankara, Turkey.
  • Kiper N; Department of Pediatric Pulmonology, School of Medicine, Hacettepe University, Ihsan Dogramaci Children's Hospital, Ankara, Turkey.
  • Demirel AH; Faculty of Sport Sciences, Department of Exercise and Sport Sciences, Exercise, and Sport Physiology Division, Hacettepe University, Ankara, Turkey.
  • Ozcelik U; Department of Sport Medicine, Hacettepe University, Ankara, Turkey.
Eur J Pediatr ; 183(5): 2333-2342, 2024 May.
Article em En | MEDLINE | ID: mdl-38430280
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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores / Fibrose Cística / Galectina 3 Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Eur J Pediatr Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Turquia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores / Fibrose Cística / Galectina 3 Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Eur J Pediatr Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Turquia