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Multifactorial low remodeling bone disease during cyclic total parenteral nutrition
The Journal of Clinical Endocrinology and Metabolism
|January 1, 1985
Summary
Long-term total parenteral nutrition (TPN) can cause metabolic bone disease. High aluminum intake and cyclic amino acid delivery during TPN contribute to hypercalciuria and reduced bone formation.
Area of Science:
- Bone Metabolism
- Nutritional Science
- Endocrinology
Background:
- Metabolic bone disease is a known complication of long-term total parenteral nutrition (TPN).
- The exact physiopathology of TPN-associated bone disease remains poorly understood.
- This study investigates bone status in adult patients receiving cyclic TPN.
Purpose of the Study:
- To prospectively assess the bone status in adult patients undergoing long-term cyclic TPN.
- To identify potential contributing factors to metabolic bone disease in this patient population.
- To characterize the histomorphometric changes in bone tissue.
Main Methods:
- Prospective assessment of bone status in seven adult patients on cyclic TPN for a mean of 7 months.
- Measurement of calciuria, calcium balance, serum mineral and vitamin D levels, and parathyroid hormone (PTH).
- Histomorphometric analysis of bone biopsies to evaluate bone formation and resorption.
Main Results:
- All patients exhibited hypercalciuria, with six showing a negative calcium balance.
- A significant correlation was found between protein intake and calciuria.
- High aluminum load from phosphate solutions was associated with elevated serum aluminum levels.
- Bone histomorphometry revealed reduced bone formation and low trabecular bone volume, without osteomalacia.
- Two patients had elevated PTH with skeletal unresponsiveness.
Conclusions:
- Cyclic TPN is associated with hypercalciuria and negative calcium balance, potentially linked to amino acid delivery.
- High aluminum load from phosphate supplements may contribute to bone defects.
- TPN-induced metabolic bone disease presents with reduced bone formation and low bone volume, distinct from osteomalacia.