Literature DB >> 19485816

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

Heather Jared1, Kim A Boggess, Kevin Moss, Carl Bose, Richard Auten, James Beck, Steven Offenbacher.   

Abstract

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.

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Year:  2009        PMID: 19485816     DOI: 10.1902/jop.2009.080642

Source DB:  PubMed          Journal:  J Periodontol        ISSN: 0022-3492            Impact factor:   6.993


  5 in total

1.  Altered gene expression in murine placentas in an infection-induced intrauterine growth restriction model: a microarray analysis.

Authors:  Y A Bobetsis; S P Barros; D M Lin; R M Arce; S Offenbacher
Journal:  J Reprod Immunol       Date:  2010-05-16       Impact factor: 4.054

2.  Birth weight of infants of mothers with aggressive periodontitis.

Authors:  Harvey A Schenkein; Thomas E Koertge; Robert Sabatini; Carol N Brooks; John C Gunsolley
Journal:  J Periodontol       Date:  2011-08-05       Impact factor: 6.993

3.  Anticardiolipin in porphyromonas gingivalis antisera causes fetal loss in mice.

Authors:  H A Schenkein; J L Bradley; D B Purkall
Journal:  J Dent Res       Date:  2013-07-15       Impact factor: 6.116

4.  Dentists' perceptions of barriers to providing dental care to pregnant women.

Authors:  Rosanna Shuk-Yin Lee; Peter Milgrom; Colleen E Huebner; Douglas A Conrad
Journal:  Womens Health Issues       Date:  2010-09

5.  Three-dimensional measurement of periodontal surface area for quantifying inflammatory burden.

Authors:  Sa-Beom Park; So-Youn An; Won-Jeong Han; Jong-Tae Park
Journal:  J Periodontal Implant Sci       Date:  2017-06-28       Impact factor: 2.614

  5 in total

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