Literature DB >> 25865080

Mineral status of premature infants in early life and linear growth at age 3.

Tsuyoshi Isojima1, Reiko Kushima2, Keiji Goishi1, Shinya Tsuchida1,2, Toyoko Watanabe2, Naoto Takahashi1, Sachiko Kitanaka1.   

Abstract

BACKGROUND: Preterm infants are at significant risk of reduced bone mineral content and subsequent bone disease (metabolic bone disease of prematurity, MBDP). MBDP is frequently found in very low-birthweight (VLBW) infants, but long-term height prognosis is not well known.
METHODS: VLBW infants from two major neonatal intensive care units were studied. Medical records were reviewed. A total of 143 subjects were analyzed after excluding subjects who died, or who had severe complications that could affect linear growth, Silver-Russell syndrome, severe cholestasis, and/or chromosomal abnormality. The relationship between MBDP and height at age 3 was investigated.
RESULTS: Height standard deviation score (SDS) at age 3 negatively correlated with peak serum alkaline phosphatase (ALP) activity in early life (r = -0.30, P = 0.0003) and positively correlated with serum phosphorus (P) at peak ALP (r = 0.33, P = 0.0002). In addition, serum P independently affected height SDS at 3 years of age (β = 0.19, P = 0.018), and was significantly different between infants with and without catch-up growth in height (difference: 0.23 mmol/L, 95%CI: 0.09-0.36, P = 0.0010).
CONCLUSIONS: MBDP, particularly hypophosphatemia in the early period of life, is associated with linear growth until 3 years of age in VLBW infants.
© 2015 Japan Pediatric Society.

Entities:  

Keywords:  metabolic bone disease of prematurity; mineral supplementation; short stature; very low-birthweight infant

Mesh:

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Year:  2015        PMID: 25865080     DOI: 10.1111/ped.12657

Source DB:  PubMed          Journal:  Pediatr Int        ISSN: 1328-8067            Impact factor:   1.524


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