Preterm birth and/or low birth weight are associated with periodontal disease and the increased placental immunohistochemical expression of inflammatory markers

Histol Histopathol. 2016 Feb;31(2):231-7. doi: 10.14670/HH-11-671. Epub 2015 Sep 29.

Abstract

The objective of this study was to determine whether gynecological and periodontal clinical parameters and the immunohistochemical expression in placental chorionic villi of the markers cyclooxygenase-2 (COX-2), interleukin (IL)-1β, vascular endothelial growth factor receptor 1 (VEGFR1), podoplanin, and Heat Shock Protein 70 (HSP70) are associated with preterm birth (PB) and/or low birth weight (LBW) neonates.

Material and methods: An observational case-control study was performed in 130 puerperal women: mothers of PB/LBW neonates (cases, n=65) and mothers of full-term normal-weight neonates (controls, n=65). Data were gathered from all participants on socio-demographic, gynecological, and periodontal variables and on placental immunohistochemical COX-2, IL-1β, VEGFR1, podoplanin, and HSP70 expression.

Results: Among the 42 women with mild/moderate periodontitis or gingivitis, the studied periodontal variables were significantly worse and the placental COX-2 (p=0.043), HSP70 (p=0.001), IL-1β (p=0.001), VEGFR1 (p=0.032), and podoplanin (p=0.058) expressions were significantly higher in the cases than in the controls. In comparison to the mothers without periodontitis, only COX-2 (p=0.026) and VEGFR1 (p=0.005) expressions were significantly increased in those with the disease. Increased COX-2 values were detected in the women with a history of genitourinary infection (p=0.036), premature rupture of membrane (p=0.012), or drug treatment (p=0.050).

Conclusions: The etiology of preterm birth and/or low birth weight is multifactorial and involves consumption habits, social-health factors, and infectious episodes. These adverse pregnancy outcomes were associated with periodontitis and the increased placental expression of IL-1β, COX-2, VEGFR1, and HSP70.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / metabolism
  • Case-Control Studies
  • Chronic Disease
  • Cyclooxygenase 2 / metabolism
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation*
  • HSP70 Heat-Shock Proteins / metabolism
  • Humans
  • Immunohistochemistry
  • Infant, Low Birth Weight*
  • Infant, Newborn
  • Inflammation
  • Interleukin-1beta / metabolism
  • Membrane Glycoproteins / metabolism
  • Periodontal Diseases / complications*
  • Periodontal Diseases / physiopathology
  • Periodontitis / metabolism
  • Placenta / metabolism*
  • Pregnancy
  • Pregnancy Complications
  • Pregnancy Outcome
  • Premature Birth*
  • Vascular Endothelial Growth Factor Receptor-1 / metabolism

Substances

  • Biomarkers
  • HSP70 Heat-Shock Proteins
  • IL1B protein, human
  • Interleukin-1beta
  • Membrane Glycoproteins
  • PDPN protein, human
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Vascular Endothelial Growth Factor Receptor-1