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Scanning Skeletal Remains for Bone Mineral Density in Forensic Contexts
Published on: January 29, 2018
Bone turnover in preterm infants
K E Naylor1, R Eastell, K E Shattuck
1Bone Metabolism Group, University of Sheffield, England.
Insights
Total parenteral nutrition (TPN) increases bone turnover in preterm infants, indicating potential bone loss. Aluminum in TPN solutions at studied levels did not impede bone formation in these vulnerable infants.
Area of Science:
- Neonatalogy
- Pediatric Endocrinology
- Biochemistry
Background:
- Total parenteral nutrition (TPN) is linked to osteopenia in preterm infants.
- Potential causes include calcium/phosphate insufficiency and aluminum contamination affecting bone health.
- Preterm infants require careful monitoring of bone metabolism during TPN.
Purpose of the Study:
- To assess biochemical markers of bone turnover in preterm infants receiving TPN.
- To compare bone turnover markers between preterm and term infants.
- To investigate the impact of aluminum in TPN on bone metabolism.
Main Methods:
- Collected serum and urine samples from preterm and term infants.
- Measured urinary pyridinium cross-links and N-telopeptide of type I collagen for bone resorption.
- Assessed serum osteocalcin for bone formation in preterm infants.
Main Results:
- N-telopeptide of type I collagen was significantly higher in preterm infants at baseline.
- All measured bone turnover markers increased significantly in preterm infants within 3 weeks.
- Aluminum levels in TPN did not inhibit bone formation at the administered concentrations.
Conclusions:
- Preterm infants on TPN exhibit elevated bone resorption and overall bone turnover.
- TPN management requires attention to bone health in preterm neonates.
- The studied aluminum levels in TPN were not detrimental to bone formation.
Abstract:
Total parenteral nutrition is associated with osteopenia in preterm infants. Insufficient calcium and phosphate are likely causes: aluminum contamination is another possible contributing factor as this adversely affects bone formation and mineralization. The study was designed to evaluate changes in biochemical markers of bone turnover in 22 preterm infants receiving total parenteral nutrition in comparison with 19 term infants. We collected urine and serum samples from 22 preterm infants, mean gestational age 29 wk, within 48 h and again at 3 wk of life. We also collected urine samples from 19 term infants, mean gestational age 39 wk, during the first day of life. Bone resorption was assessed by the measurement of urinary pyridinium cross-links by HPLC and ELISA and the N-telopeptide of type I collagen by ELISA. Bone formation was assessed in premature infants by the measurement of serum osteocalcin. The N-telopeptide of type I collagen was higher in the preterm infants compared with term at baseline (p < 0.01). There was no difference between the pyridinium cross-links in the preterm and term infants. All the biochemical markers of bone turnover increased significantly in the preterm infants during the first 3 wk of life, e.g. N-telopeptide was a 153% change from baseline (p < 0.001). Aluminum in the total parenteral nutrition solutions did not cause a decrease in bone formation at the level administered (3-6 microg, 0.1-0.2 micromol x kg(-1) x d(-1)).
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