Salivary cotinine and S100A8/A9 levels in children exposed to environmental tobacco smoke: a case-control study


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Kockanat A., Acıpınar Ş.

JOURNAL OF APPLIED ORAL SCIENCE, cilt.34, ss.1-9, 2026 (SCI-Expanded)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 34
  • Basım Tarihi: 2026
  • Doi Numarası: 10.1590/1678-7765-2025-0840
  • Dergi Adı: JOURNAL OF APPLIED ORAL SCIENCE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED)
  • Sayfa Sayıları: ss.1-9
  • Sivas Cumhuriyet Üniversitesi Adresli: Evet

Özet

Exposure to environmental tobacco smoke (ETS) poses significant risks to children’s oral health by inducing oxidative

stress and triggering inflammatory responses. Even in the absence of clinically evident oral inflammation, early biological

changes can be detected in children exposed to ETS. Objectives: This study aimed to evaluate salivary cotinine and

S100A8/A9 levels in children exposed to ETS and to examine the relationship between exposure intensity and inflammatory

biomarker expression. Methodology: This observational case-control study included 150 systemically healthy children

aged 6–12 years. ETS exposure was determined using parent-reported questionnaires. Clinical parameters, including

plaque index, gingival index, and probing pocket depth, were recorded. Unstimulated saliva samples were analyzed for

cotinine, S100A8, and S100A9 using ELISA kits. Group comparisons were conducted using the Mann–Whitney U test, and

correlations were assessed using Spearman’s rank correlation coefficient. Statistical significance was set at p<0.05. Results:

ETS-exposed and non-exposed groups did not differ significantly in age, sex, socioeconomic status, oral hygiene habits,

or clinical periodontal parameters (p>0.05). However, salivary cotinine, S100A8, and S100A9 levels were significantly

higher in ETS-exposed children (p<0.05). Cotinine demonstrated a moderate positive correlation with S100A8, while its

correlation with S100A9 was weak and non-significant. Exposure intensity was positively associated with cotinine and

S100A8 levels, but not with S100A9. Conclusion: ETS exposure in children is associated with early biochemical signs of

inflammation, even in the absence of clinically detectable periodontal changes. Elevated salivary cotinine and S100A8

levels highlight the potential utility of salivary biomarkers for identifying subclinical effects of passive smoking. These

findings underscore the importance of interventions aimed at reducing children’s exposure to ETS to protect long-term

oral health. Clinical trial registration: NCT06791707