Small-for-gestational-age preterm-born infants already have lower bone mass during early infancy

Monique van de Lagemaat1, Joost Rotteveel, Mirjam M van Weissenbruch

  • 1Department of Pediatrics, VU University Medical Center, Amsterdam, The Netherlands. m.vandelagemaat@vumc.nl

Bone
|July 4, 2012
PubMed

Insights

Preterm infants who are small-for-gestational-age (SGA) exhibit reduced bone mineral content (BMC) and bone accretion during infancy. This suggests prenatal factors crucial for bone development are not fully compensated for postnatally.

Area of Science:

  • Pediatrics
  • Neonatology
  • Bone Biology

Background:

  • Low birth weight in preterm infants is linked to diminished peak bone mass.
  • The association between low birth weight and bone mass during infancy remains unclear.

Purpose of the Study:

  • To investigate the impact of birth weight on bone accretion in preterm infants from term age to six months post-term.
  • To compare bone mineral content (BMC) and accretion in small-for-gestational-age (SGA) versus appropriate-for-gestational-age (AGA) preterm infants.

Main Methods:

  • Whole-body bone mineral content (BMC) was measured in 139 preterm infants at term age and six months post-term.
  • Infants were categorized at birth as SGA (n=33) or AGA (n=98) based on weight and length SDS.
  • Statistical adjustments were made for gender, gestational age, and actual body size.

Main Results:

  • SGA infants had significantly lower BMC than AGA infants at term age and six months post-term, even after adjusting for covariates.
  • BMC gain between term age and six months post-term was also lower in SGA infants compared to AGA infants.
  • This difference in BMC gain persisted even after adjusting for weight and length gain, indicating an independent effect.

Conclusions:

  • Small-for-gestational-age preterm infants experience impaired bone accretion in the first six months post-term.
  • The findings suggest that the prenatal environment plays a critical role in bone development that cannot be fully replicated postnatally.
  • This highlights potential long-term implications for bone health in SGA preterm infants.
Abstract

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