Relationships between cotinine, lower respiratory tract infection, and eosinophil cationic protein in children

Pembe Keskinoglu1, Dilek Cimrin, Gazanfer Aksakoglu

  • 1School of Medicine, Department of Public Health, Dokuz Eylül University, 35340, Inciralti/Izmir, Turkey. pembekeskin@yahoo.com

Insights

Passive smoking significantly increases the risk of lower respiratory tract infections (LRTI) in children. Exposure to secondhand smoke is linked to higher urine eosinophil cationic protein (u-ECP) levels, indicating airway inflammation.

Area of Science:

  • Environmental Health
  • Pediatrics
  • Respiratory Medicine

Background:

  • Passive smoking is a significant environmental exposure in children.
  • Lower respiratory tract infections (LRTI) are a common pediatric health concern.
  • Airway inflammation is a key feature of respiratory illnesses.

Purpose of the Study:

  • To investigate the association between passive smoking and urine eosinophil cationic protein (u-ECP) levels in children with LRTI.
  • To determine if passive smoking contributes to airway inflammation in pediatric LRTI cases.

Main Methods:

  • A case-control study involving 150 children with LRTI and 150 healthy controls.
  • Measurement of urine cotinine (biomarker for passive smoking) and u-ECP levels.
  • Statistical analysis using t-test, McNemar chi-square test, and Pearson correlation.

Main Results:

  • A high prevalence of passive smoking was observed in both children with LRTI and healthy controls.
  • Passive smoking was associated with a 4.7-fold increased prevalence of LRTI (p=0.000).
  • Children with LRTI exhibited significantly higher mean u-ECP levels (p=0.018) and a positive correlation between u-cotinine and u-ECP.

Conclusions:

  • Passive smoking plays a crucial role in the development of respiratory infections in children.
  • Secondhand smoke exposure contributes to airway inflammation in children with LRTI.
  • u-ECP serves as a potential biomarker for assessing passive smoking-induced airway inflammation in pediatric LRTI.
Abstract

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