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Published on: November 20, 2015
Bronchopulmonary dysplasia is associated with delayed structural brain maturation in preterm infants
Vera Neubauer1, Daniel Junker, Elke Griesmaier
1Neonatology, Department of Paediatrics II, Innsbruck Medical University, Innsbruck, Austria.
Insights
Bronchopulmonary dysplasia (BPD) is linked to delayed brain maturation in very preterm infants. This finding highlights additional neural correlates of adverse outcomes beyond common brain injuries.
Area of Science:
- Neonatal Neurology
- Neuroimaging
- Developmental Pediatrics
Background:
- Cerebral magnetic resonance imaging (MRI) is crucial for assessing preterm brain injury.
- MRI at term-equivalent age (TEA) reveals delayed brain maturation in preterm infants, impacting neurobehavioral outcomes.
Purpose of the Study:
- To examine how common neonatal risk factors influence structural brain maturation in very preterm infants at TEA.
- To identify specific neonatal conditions associated with delayed brain maturation.
Main Methods:
- 130 very preterm infants (mean gestational age 29.7 weeks) underwent MRI at TEA.
- A validated 'total maturation score' was assigned to assess brain development.
- Brain maturation scores were correlated with neonatal data.
Main Results:
- Bronchopulmonary dysplasia (BPD), late-onset sepsis, and retinopathy of prematurity were associated with delayed brain maturation.
- Infants with delayed maturation required longer ventilation and experienced more severe hypotension.
- BPD remained a significant predictor of delayed brain maturation in multivariate analysis.
Conclusions:
- Delayed structural brain maturation at TEA is preceded by BPD in very preterm infants.
- BPD is a predictor of adverse outcomes, and this study links it to delayed brain maturation.
- Adverse outcomes in preterm infants may involve neural correlates beyond typical brain injury.
Background:
In recent years, cerebral magnetic resonance imaging (MRI) has been increasingly used to depict the wide spectrum of preterm brain injury. Furthermore, it has already been demonstrated by MRI at term-equivalent age (TEA) that preterm infants show delayed brain maturation as compared to term infants, and this delay has been related to neurobehavioral outcome.
Objectives:
The aim of the current study was to investigate the influence of prevalent neonatal risk factors for adverse outcome on structural brain maturation in very preterm infants at TEA.
Methods:
One hundred and thirty very preterm infants born at a mean gestational age of 29.7 weeks were included. MRI was performed at TEA and given a validated 'total maturation score'. Brain maturation scores were compared with neonatal data.
Results:
In univariate analysis, bronchopulmonary dysplasia (BPD), late-onset sepsis and retinopathy of prematurity were significantly associated with delayed brain maturation. Furthermore, infants with delayed maturation had been ventilated significantly longer and more often suffered from severe arterial hypotension. In multivariate analysis, BPD remained significant as predictor of delayed brain maturation.
Conclusions:
This study is the first to show that delayed structural brain maturation as evaluated by MRI at TEA is preceded by BPD, which is known to be a predictor of adverse outcome in preterm infants. This finding adds further evidence to show that adverse outcome in preterm infants may have additional neural correlates that exceed common brain injury.
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