Fetal exposure to oral pathogens and subsequent risk for neonatal intensive care admission.


Journal Article

BACKGROUND: Maternal periodontal infection has been associated with adverse maternal and neonatal outcomes. In utero fetal exposure to oral pathogens was also recognized as deleterious to the fetus. The objective of this study was to determine the relationship between fetal exposure to oral pathogens and neonatal intensive care unit (NICU) admission. METHODS: This was a secondary analysis of a prospective cohort study of maternal oral health and pregnancy outcome. Fetal immunoglobulin M against oral pathogens was detected in umbilical cord serum by immunoblot. The presence of at least one oral pathogen-specific antibody was considered seropositivity. The cord level of C-reactive protein was determined by enzyme-linked immunosorbent assay and categorized as detectable versus undetectable. Chi-square and logistic regression analyses were used to determine the association between cord serum seropositivity or detectable C-reactive protein and NICU admission and length of stay. RESULTS: Of 650 infants, 45 (6.9%) were admitted to the NICU. The admission rate was higher among seropositive infants compared to seronegative infants (11% versus 5%; P = 0.0019). Seropositive infants were also more likely than seronegative infants to stay >3 or >7 days (8% versus 3% and 6% versus 2%; P = 0.004 and 0.003, respectively). Adjusting for gestational age, the odds ratio (95% confidence interval) for NICU admission was 2.14 (1.01 to 4.54); for a length of stay >3 or >7 days, it was 2.38 (1.01 to 5.60) and 3.29 (1.13 to 9.58), respectively. The NICU admission rate was not significantly higher for those with detectable versus undetectable umbilical cord serum C-reactive protein (8% versus 6%; P = 0.3). CONCLUSIONS: In utero fetal exposure to oral pathogens increases the risk for NICU admission and the length of stay. Interventions that interrupt fetal exposure to oral pathogens may reduce these risks.

Full Text

Cited Authors

  • Jared, H; Boggess, KA; Moss, K; Bose, C; Auten, R; Beck, J; Offenbacher, S

Published Date

  • June 2009

Published In

Volume / Issue

  • 80 / 6

Start / End Page

  • 878 - 883

PubMed ID

  • 19485816

Pubmed Central ID

  • 19485816

Electronic International Standard Serial Number (EISSN)

  • 1943-3670

International Standard Serial Number (ISSN)

  • 0022-3492

Digital Object Identifier (DOI)

  • 10.1902/jop.2009.080642


  • eng