Periodontopathogenic microbiota, infectious mechanisms and preterm birth: analysis with structural equations

Elisa Miranda Costa1, Camilla Silva de Araujo Figueiredo2, Rafiza Félix Marão Martins3

  • 1Department of Public Health, Federal University of Maranhão, Rua Barão de Itapary, 155 - Centro, São Luís, Maranhão, CEP 65020-070, Brazil. elisamirandac@hotmail.com.

Insights

Periodontopathogenic bacteria burden did not directly link to preterm birth (PTB). However, lower levels of IL-10 and TGF-β cytokines, along with other systemic infections during pregnancy, were associated with increased PTB risk.

Area of Science:

  • Obstetrics and Gynecology
  • Periodontology
  • Immunology

Background:

  • The link between periodontopathogenic microbiota and preterm birth (PTB) is established, yet underlying biological mechanisms remain unclear.
  • Understanding these mechanisms is crucial for developing targeted interventions to prevent PTB.

Purpose of the Study:

  • To investigate the influence of periodontopathogenic bacteria burden (PBB), periodontal disease, and other infections during pregnancy on PTB.
  • To elucidate the role of specific cytokines (IL-10, TGF-β) in the relationship between these factors and PTB using Structural Equation Modeling.

Main Methods:

  • A case-control study nested within the prospective BRISA cohort, including 110 PTB cases and 220 controls.
  • Data collected on cytokines (IL-10, TGF-β), periodontal disease, PBB, age, socioeconomic status, and systemic infections.
  • Correlations analyzed using Standardized Coefficient (SC) within a Structural Equation Model framework.

Main Results:

  • Increased PBB was associated with periodontal disease but not directly with PTB or the studied cytokines.
  • Lower serum levels of IL-10 and TGF-β were significantly correlated with a higher occurrence of PTB.
  • Presence of other systemic infections during pregnancy also independently predicted higher PTB occurrence.

Conclusions:

  • Severe periodontal disease and other systemic infections may influence PTB by altering the inflammatory cytokine cascade.
  • The direct impact of PBB on PTB appears mediated by other factors, potentially including systemic inflammation and immune response modulation.
Abstract