Effects of Posthemorrhagic Ventricular Dilatation in the Preterm Infant on Brain Volumes and White Matter Diffusion

Margaretha J Brouwer1, Linda S de Vries1, Karina J Kersbergen2

  • 1Department of Neonatology, Wilhelmina Children's Hospital, Utrecht, The Netherlands; Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.

The Journal of Pediatrics
|November 4, 2015
PubMed

Insights

Posthemorrhagic ventricular dilatation (PHVD) in preterm infants is linked to reduced deep gray matter and cerebellar volumes, and altered white matter diffusion. Germinal matrix-intraventricular hemorrhage (GMH-IVH) alone did not show these effects.

Area of Science:

  • Neonatal neurology
  • Neuroimaging
  • Developmental neuroscience

Background:

  • Germinal matrix-intraventricular hemorrhage (GMH-IVH) is a common complication in preterm infants.
  • Posthemorrhagic ventricular dilatation (PHVD) can develop following GMH-IVH, potentially impacting brain development.
  • Understanding the distinct effects of GMH-IVH and PHVD is crucial for targeted interventions.

Purpose of the Study:

  • To compare the effects of GMH-IVH and PHVD on brain and cerebrospinal fluid (CSF) volumes.
  • To assess the impact of GMH-IVH and PHVD on white matter diffusion characteristics.
  • To evaluate these effects at term-equivalent age (TEA) in preterm infants.

Main Methods:

  • A case-control study involving preterm infants (gestational age <31 weeks) with GMH-IVH grade II-III and PHVD requiring intervention.
  • Comparison groups included infants with GMH-IVH grade II without PHVD and infants without GMH-IVH.
  • Magnetic resonance imaging (MRI) at TEA assessed brain tissue volumes, CSF volumes, and apparent diffusion coefficients (ADCs) in white matter and cerebellum.

Main Results:

  • PHVD was significantly associated with reduced deep gray matter and cerebellar volumes.
  • PHVD was also linked to increased ventricular and extracerebral CSF volumes.
  • Increased white matter ADC values were observed in infants with PHVD, indicating altered diffusion.

Conclusions:

  • PHVD, even after intervention, negatively impacts deep gray matter and cerebellar volumes and alters white matter microstructure.
  • GMH-IVH alone, without significant PHVD, did not demonstrate these adverse effects on brain volumes or diffusion at TEA.
  • These findings highlight PHVD as a distinct pathological entity with significant neurodevelopmental consequences in preterm infants.
Abstract

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