Neurodevelopment Outcomes in Very-Low-Birth-Weight Infants with Metabolic Bone Disease at 2 Years of Age

Yu-Wen Chen1, Yu-Jun Chang2, Lih-Ju Chen1

  • 1Department of Neonatology, Changhua Christian Children's Hospital, No. 320, Xuguang Road, Changhua City 500010, Taiwan.

PubMed

Insights

Metabolic bone disease (MBD) in very-low-birth-weight (VLBW) infants is linked to poorer neurodevelopmental outcomes. This study found MBD negatively impacts motor, language, and cognitive development at two years corrected age.

Area of Science:

  • Neonatology
  • Pediatric Bone Health
  • Neurodevelopmental Pediatrics

Background:

  • Metabolic bone disease (MBD) is common in preterm infants, especially very-low-birth-weight (VLBW) infants (<1500 g).
  • Limited data exists on the relationship between MBD and neurodevelopmental outcomes in this vulnerable population.
  • Understanding these links is crucial for early intervention and improved long-term health.

Purpose of the Study:

  • To identify risk factors for MBD in VLBW infants.
  • To evaluate the impact of MBD on neurodevelopmental outcomes at 2 years corrected age.
  • To provide insights into the long-term consequences of MBD in VLBW infants.

Main Methods:

  • Retrospective assessment of 749 VLBW infants (<1350 g) using radiographic signs for MBD diagnosis.
  • Neurodevelopmental assessment using the Bayley Scales of Infant Development, Third Edition (BSID-III) at 6, 12, and 24 months corrected age.
  • Exclusion of infants with major congenital or chromosomal abnormalities and those lost to follow-up.

Main Results:

  • 97 VLBW infants were diagnosed with MBD.
  • Infants with MBD showed significantly lower scores in motor, language, and cognitive domains at 24 months corrected age compared to those without MBD.
  • 86% of enrolled infants completed all three follow-up assessments.

Conclusions:

  • Metabolic bone disease in VLBW infants is associated with impaired neurodevelopmental outcomes.
  • Cognitive, motor, and language composite scores are negatively affected by MBD at 24 months corrected age.
  • Early identification and management of MBD may be critical for optimizing neurodevelopmental trajectories in VLBW infants.