AI Article Synopsis

  • Environmental tobacco smoke (ETS) exposure is linked to changes in cytokine levels in hospitalized children, with a focus on measuring inflammatory markers and cotinine in saliva.
  • A study involving 112 nonsmoking children found that those with higher cotinine levels, indicating more ETS exposure, exhibited elevated IL-1β levels, especially when cotinine levels exceeded 5 ng/mL.
  • Results suggest that higher ETS exposure can enhance pro-inflammatory immune responses in children, potentially hindering their immune function and recovery from illnesses.

Article Abstract

Environmental tobacco smoke (ETS) exposure is associated with altered cytokine levels in children. We sought to examine ETS exposure prevalence and the relationship between ETS exposure and cytokine levels in a sample of hospitalized children. (2) Methods: Inflammatory markers (IL-8, IL-1β, IL-10, and TNF-α) and cotinine were measured in saliva of hospitalized, nonsmoking children (N = 112). To assess the association between ETS exposure and immune system response, we built a multivariate regression model including the four inflammatory markers as the response variables and cotinine, age, sex, and discharge diagnosis as explanatory variables while assessing possible interaction effects. (3) Results: Mean age (SD) was 5.8(5.0) years; Geometric Mean (GeoM) cotinine = 1.8 [95% CI = 1.4-2.2]. Children with non-inflammatory other diagnoses had lower IL-10 ( = 0.003) and TNF-α ( = 0.009) levels than children with inflammatory other diagnoses. Children with asthma ( = 0.01) and bacterial illnesses and/or pneumonia ( = 0.002) had higher IL-8 levels. Independent of diagnosis, there was a significant curvilinear association between cotinine and IL-1β ( = 0.002) reflecting no association for cotinine levels <5 ng/mL and a positive association for >5 ng/mL. (4) Conclusions: Children with higher ETS exposure levels have higher IL-1β levels regardless of age, sex, and diagnosis. ETS exposure may increase pro-inflammatory immune responses in children and may interfere with native immune responses and the ability to heal and fight infection.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6926853PMC
http://dx.doi.org/10.3390/ijerph16234625DOI Listing

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