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Catch-up growth with normal parathyroid hormone levels in chronic renal failure
Simon Waller1, Sarah Ledermann, Richard Trompeter
1Department of Nephro-Urology, Institute of Child Health and Great Ormond Street Hospital for Children NHS Trust, 30 Guilford Street, London WC1N 1EH, UK. swaller@doctors.net.uk
Insights
Normalizing parathyroid hormone (PTH) levels in children with chronic renal failure (CRF) may promote catch-up growth. This study found improved height standard deviation scores in pediatric CRF patients when PTH levels were managed.
Area of Science:
- Pediatric Nephrology
- Endocrinology
- Growth and Development
Background:
- The optimal range for parathyroid hormone (PTH) in pediatric chronic renal failure (CRF) is not well-defined.
- Growth impairment is a common complication in children with CRF.
Purpose of the Study:
- To assess growth velocity in children with CRF managed towards normal PTH levels.
- To investigate the relationship between PTH levels and growth in pediatric CRF.
Main Methods:
- Retrospective review of 99 children with CRF (GFR <41 ml/min per 1.73 m(2)) and at least 2 years of follow-up.
- Data collected on glomerular filtration rate (GFR), serum calcium, phosphate, PTH, and height standard deviation score (Ht SDS).
- Analysis of growth changes in relation to various clinical parameters.
Main Results:
- Children with CRF achieved a mean change in Ht SDS of +0.3, significantly greater than expected (P=0.004).
- Median PTH levels were at the upper limit of normal, with serum calcium and phosphate near mid-normal ranges.
- Growth rate was not significantly correlated with age, PTH levels, enteral feeds, or 1-alpha calcidol dosage.
Conclusions:
- Medical therapy targeting normalized PTH levels can facilitate catch-up growth in pediatric CRF patients.
- Achieving normal PTH levels appears crucial for improving growth velocity in children with chronic renal failure.
Abstract:
The optimum range for parathyroid hormone (PTH) levels in children with chronic renal failure (CRF) remains undefined. We aimed to determine growth velocity in children with CRF managed with normal PTH levels. We performed a retrospective case note review of 99 children (77 boys), with a glomerular filtration rate (GFR) <41 ml/min per 1.73 m(2), who had at least 2 years of 3-monthly follow-up. The age range at entry was 0.5-6.0 years; data collection was continued until 10 years of age or the commencement of growth hormone or renal replacement therapy. The median GFR was 22 ml/min per 1.73 m(2); over the study period mean serum calcium and phosphate levels were approximately equal to the mid-point of the respective normal ranges. Median PTH levels were equal to the upper limit of the normal range. Height standard deviation score (Ht SDS) at entry was -1.73. During the study period the overall mean change in Ht SDS was +0.3, significantly greater than the no change expected of a normal population ( P=0.004). The median dose of calcium carbonate was 150 mg/kg per day and 1-alpha calcidol 0.015 microg/kg per day. The growth rate was independent of all parameters, including age, PTH levels, the use of enteral feeds, and 1-alpha calcidol prescription. Our results indicate that catch-up growth can occur in infants and children with CRF when medical therapy is aimed at normalizing PTH levels.
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