Abstract
Background: The associations between nitrogen metabolism and bone turnover during bed rest are still not completely understood. Methods: We measured nitrogen balance (nitrogen intake minus urinary nitrogen excretion) and biochemical metabolic markers of calcium and bone turnover in six males before head-down tilt bed rest (baseline), during 2, 10, and 14 weeks of immobilization, and after reambulation. Results: The changes in nitrogen balance were highest between baseline and week 2 (net change, -5.05 ± 1.30 g/day; 3.6 ± 0.6 g/day at baseline vs -1.45 ± 1.3 g/day at week 2; P <0.05). In parallel, serum intact osteocalcin (a marker of bone formation) was already reduced and renal calcium and phosphorus excretions were increased at week 2 (P <0.05). Fasting serum calcium and phosphorus values and renal excretion of N-telopeptide (a bone resorption marker) were enhanced at weeks 10 and 14 (P <0.05-0.001), whereas serum concentrations of parathyroid hormone, calcitriol, and type I collagen propeptide (a marker of bone collagen formation) were decreased at week 14 (P <0.05-0.01). Significant associations were present between changes of serum intact osteocalcin and 24-h calcium excretion (P <0.001), nitrogen balance and 24-h phosphorus excretion (P <0.001), nitrogen balance and renal N-telopeptide excretion (P <0.05), and between serum osteocalcin and nitrogen balance (P <0.025). Conclusions: Bone formation decreases rapidly during immobilization in parallel with a higher renal excretion of intestinally absorbed calcium. These changes appear in association with the onset of a negative nitrogen balance, but decreased bone collagen synthesis and enhanced collagen breakdown occur after a time lag of several weeks. © 2001 American Association for Clinical Chemistry.
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CITATION STYLE
Scheld, K., Zittermann, A., Heer, M., Herzog, B., Mika, C., Drummer, C., & Stehle, P. (2001). Nitrogen metabolism and bone metabolism markers in healthy adults during 16 weeks of bed rest. Clinical Chemistry, 47(9), 1688–1695. https://doi.org/10.1093/clinchem/47.9.1688
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