Microbiologic and histologic characteristics of the extremely preterm infant's placenta predict white matter damage

Alan Leviton1, Elizabeth N Allred, Karl C K Kuban

  • 1Department of Neurology, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts 02115, USA.

Pediatric Research
|September 12, 2009
PubMed

Insights

Low-virulence placental microorganisms, including skin flora, predict brain lesions and cerebral palsy (CP) in preterm infants. Placental inflammation also predicts these outcomes, independent of organism recovery.

Area of Science:

  • Neonatal neurology
  • Perinatal medicine
  • Microbiology

Background:

  • Inflammatory processes are implicated in perinatal brain damage and cerebral palsy (CP).
  • The specific triggers for this inflammation remain largely unknown.
  • Understanding these triggers is crucial for preventing adverse neurodevelopmental outcomes in preterm infants.

Purpose of the Study:

  • To investigate the association between placental microbial findings and neonatal brain lesions.
  • To determine the predictive value of placental inflammation and microbial cultures for neurological outcomes, specifically diparetic CP.
  • To explore the interplay between microbial presence and inflammation in predicting brain abnormalities.

Main Methods:

  • Analysis of placental biopsies and cultures from 1246 infants born before 28 weeks gestation.
  • Cerebral ultrasound scans performed on all infants, with readings by two independent sonologists.
  • Neurological examinations conducted at approximately 24 months postterm equivalent for 899 infants.
  • Histological examination of placental slides to assess inflammation.

Main Results:

  • Recovery of a single microorganism predicted echolucent brain lesions.
  • Polymicrobial cultures and skin flora predicted ventriculomegaly and echolucent lesions.
  • Single microorganisms, multiple organisms, and skin flora all predicted diparetic CP.
  • Histologic inflammation independently predicted ventriculomegaly and diparetic CP.
  • The combination of organism recovery and inflammation heightened the risk of ventriculomegaly but not diparetic CP.

Conclusions:

  • Low-virulence microorganisms from the placenta, including skin flora, are associated with ultrasound-detected brain lesions and diparetic CP in very preterm infants.
  • Placental inflammation can predict diparetic CP even without detectable organism recovery.
  • These findings highlight the role of the placental microbiome and inflammatory response in neonatal brain injury and CP development.

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