Air pollution might affect the clinical course of COVID-19 in pediatric patients

Ecotoxicol Environ Saf. 2022 Jul 1:239:113651. doi: 10.1016/j.ecoenv.2022.113651. Epub 2022 May 17.

Abstract

Air pollution, to which children are more susceptible than adults, can promote airway inflammation, potentially exaggerating the effects of respiratory viral infection. This study examined the association between the clinical manifestation of COVID-19 in unvaccinated pediatric patients hospitalized in Poland (n = 766) and levels of particulate matter 2.5 (PM2.5) and benzo(a)pyrene (B(a)P) within a week before hospitalization. Children aged ≤ 12 years exposed to mean and max 24 h B(a)P levels > 1 ng/m3 revealed higher odds of cough, dyspnea, fever, and increased concentrations of inflammatory markers (C-reactive protein, interleukin-6, procalcitonin, white blood cell count). In older patients (13-17 years), elevated mean 24 h B(a)P levels increased odds of dyspnea, fever, and diarrhea, and higher concentrations of C-reactive protein and procalcitonin. Exposure to max 24 h PM2.5 levels > 20 µg/m3 was associated with higher odds of cough, increased concentrations of C-reactive protein (group ≤12 years), and increased procalcitonin concentration (groups ≤12 years and 13-17 years). In both age groups, length of stay was extended in patients exposed to elevated levels of max 24 h PM2.5, mean and max 24 h B(a)P. This study suggests that worse air quality, particularly reflected in increased B(a)P levels, might affect the clinical course of COVID-19 in pediatric patients and adds to the disease burden during a pandemic.

Keywords: Benzo(a)pyrene; Epidemiology; Inflammation; Pandemic; Particulate matter; Pediatric.

MeSH terms

  • Adolescent
  • Air Pollution* / adverse effects
  • Air Pollution* / analysis
  • C-Reactive Protein
  • COVID-19* / diagnosis
  • Child
  • Cough / epidemiology
  • Cough / etiology
  • Dyspnea / epidemiology
  • Dyspnea / etiology
  • Environmental Exposure / analysis
  • Humans
  • Particulate Matter* / adverse effects
  • Particulate Matter* / analysis
  • Procalcitonin

Substances

  • Particulate Matter
  • Procalcitonin
  • C-Reactive Protein