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Updated: Aug 19, 2026

Comparative Analysis of Human Growth Hormone in Serum Using SPRi, Nano-SPRi and ELISA Assays
Published on: January 7, 2016
Growth hormone for children with chronic renal failure and on dialysis
1Pediatrics Department, King AbdulAziz University Hospital, PO Box 80215, 21589, Jeddah, Saudi Arabia. jkari@doctors.org.uk
Insights
Recombinant human growth hormone (rhGH) improved height in children with chronic renal failure (CRF) for up to three years. Growth hormone therapy showed benefits for conservatively managed children and those on dialysis, with limited changes post-transplantation.
Area of Science:
- Pediatric Nephrology
- Endocrinology
- Growth Hormone Therapy
Background:
- Chronic renal failure (CRF) in children often leads to growth impairment.
- Recombinant human growth hormone (rhGH) is a potential therapeutic option for growth deficits in pediatric CRF.
Purpose of the Study:
- To evaluate the efficacy of rhGH in improving height standard deviation score (Ht SDS) in children with CRF.
- To assess the impact of rhGH on growth in children with CRF, stratified by management (conservative vs. dialysis).
Main Methods:
- Retrospective analysis of 32 children with CRF treated with rhGH for over one year.
- Comparison of Ht SDS changes in conservatively managed children versus those on hemodialysis (HD) or peritoneal dialysis (PD).
Main Results:
- Conservatively managed children showed significant Ht SDS improvement up to 3 years (P=0.001).
- Children on dialysis demonstrated significant Ht SDS improvement within the first year (P=0.02).
- Post-transplantation, rhGH discontinuation resulted in minimal Ht SDS changes over 5 years.
Conclusions:
- rhGH therapy offers a significant growth benefit for children with CRF, particularly in the conservatively managed group and during the initial year for those on dialysis.
- The growth-promoting effects of rhGH are sustained for a limited period, with limited impact after renal transplantation.
Abstract:
We studied all children with CRF who received recombinant human growth hormone (rhGH) for more than a year (mean+/-SD duration of therapy 3.7+/-2.5 years) over an 11-year period. There were 32 children. Twenty-one children were conservatively managed, with a mean glomerular filtration rate (GFR) of 24+/-12 mL min(-1)/1.73 m2 at the start of rhGH. Their height standard deviation score improved from -2.5+/-1.4 to -2.1+/-0.7 at 1 year (P=0.3), -2.0+/-0.7 at 2 years (P=0.01), and -1.6+/-0.6 at 3 years (P=0.001). After that there was no improvement. Eleven children were on dialysis, six on haemodialysis (HD) and five on peritoneal (PD). Ht SDS improved from -2.7+/-0.5 to -2.3+/-0.5 at 1 year (P=0.02). Thereafter there was no further improvement. RhGH was stopped because of transplantation in 29 patients at a mean+/-SD age of 12.1+/-4.0 years. Mean Ht SDS was -1.8+/-0.8 at transplant and there was no change over the following 5 years. In conclusion, treatment with rhGH resulted in improvement in Ht SDS in conservatively managed CRF for up to 3.0 years and for 1 year in children on dialysis. Discontinuation of rhGH after transplantation resulted in little change in Ht SDS.
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