Inflammatory mediators in saliva and gingival fluid of children with congenital heart defect

Oral Dis. 2020 Jul;26(5):1053-1061. doi: 10.1111/odi.13313. Epub 2020 Mar 24.

Abstract

Objectives: (a) To compare levels of pro- and anti-inflammatory mediators in saliva and gingival crevicular fluid (GCF) in children with and without congenital heart defects (CHD cases and controls) and to test whether a systemic component exists in CHD cases by controlling for gingivitis and plaque scores. (b) To correlate the levels of pro- and anti-inflammatory mediators in GCF and saliva with plaque bacterial composition among CHD cases and controls.

Materials and methods: Whole un-stimulated saliva and GCF samples were collected (60 CHD cases, 60 controls [Sudan]) and were analysed for levels of prostaglandin E2 (PGE2), interleukin-1β (IL-1β), tumour necrosis factor-α (TNF-α), interleukin-1ra (IL-1ra) and interleukin-10 (IL-10) levels. These levels were correlated with the previously reported levels of four red complex bacteria.

Results: Significantly elevated levels of PGE2 and IL-1β in GCF and IL-1β and TNF-α in saliva were detected among CHD cases compared with controls. General linear model (GLM) analyses revealed that PGE2 and IL-1β levels remained significantly higher in GCF and saliva samples, respectively, among CHD cases after controlling for gingivitis and plaque score, whereas TNF-α and IL-10 levels were significantly lower in their GCF samples. Additionally, IL-1β level was significantly positively correlated to the counts of the four red complex species in their GCF.

Conclusion: In addition to higher levels of some pro-inflammatory mediators in saliva and GCF corresponding to more gingivitis in CHD cases, also a systemic inflammatory component exists and is reflected in these two oral fluids.

Keywords: children; congenital heart defects; gingival crevicular fluid; gingivitis; inflammatory mediators; saliva.

MeSH terms

  • Child
  • Dental Plaque*
  • Gingival Crevicular Fluid
  • Gingivitis*
  • Heart Defects, Congenital* / immunology
  • Humans
  • Inflammation*
  • Saliva* / immunology