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Comparative Analysis of Human Growth Hormone in Serum Using SPRi, Nano-SPRi and ELISA Assays
Published on: January 7, 2016
Growth over 10 years following a 1-year trial of growth hormone therapy
1Nephrourology Unit, Great Ormond Street Hospital for Children NHS Trust, London, UK. L.Rees@ich.ucl.ac.uk
Insights
Recombinant human growth hormone (rhGH) therapy improved height standard deviation scores (Ht SDS) in short children with chronic renal failure and renal transplants. These growth improvements were maintained even after rhGH treatment was stopped.
Area of Science:
- Pediatric Endocrinology
- Nephrology
- Growth Hormone Therapy
Background:
- Children with chronic renal failure (CRF) and those who have undergone renal transplants often experience short stature.
- Recombinant human growth hormone (rhGH) is a potential therapeutic option for improving growth in these populations.
Purpose of the Study:
- To assess the long-term growth outcomes in short children with CRF and renal transplants treated with rhGH.
- To evaluate the effect of rhGH on height standard deviation scores (Ht SDS) over a 10-year follow-up period.
Main Methods:
- A 1-year trial of rhGH therapy was initiated in three groups of prepubertal and pubertal children.
- Patients included prepubertal children with CRF, prepubertal children with renal transplants, and pubertal children with renal transplants.
- Growth (Ht SDS) was monitored during rhGH treatment and over a 10-year follow-up period.
Main Results:
- In prepubertal children with CRF, Ht SDS increased significantly during rhGH therapy and was maintained at 10 years.
- Children with renal transplants showed some improvement in Ht SDS during rhGH treatment, with final heights showing statistical significance in the pubertal group after cessation of therapy.
- Overall, 13 patients who attained final height showed significant increases in Ht SDS during rhGH treatment and after stopping treatment.
Conclusions:
- The majority of short children with CRF and renal transplants experienced improved Ht SDS while on rhGH therapy.
- The positive effects on height were largely maintained after the cessation of rhGH treatment.
- Long-term follow-up revealed sustained growth benefits, suggesting rhGH is an effective treatment for growth failure in this cohort.
Abstract:
The growth of short children with chronic renal failure (CRF) and renal transplants was assessed over 10 years following entry into a 1-year trial of recombinant human growth hormone (rhGH) therapy. Patients were divided into three groups: 6 prepubertal patients with CRF (group 1), mean (range) age at start of trial 7.7 (5.0-10.4) years; 6 prepubertal patients with renal transplants (group 2), age 11.9 (9.5-14.6) years; and 6 pubertal patients with renal transplants (group 3), age 15.6 (14.1-18.3) years. In group 1, the mean (range) height standard deviation score (Ht SDS) increased from -2.9 (-3.7 to -2.2) to -1.9 (-2.9 to -0.5) over 4.0 (0.3-9.1) years of rhGH (P=0.04), and was -1.6 (-2.9 to -0.4) after 10 years of follow-up (NS). In group 2 Ht SDS increased from -3.3 (-4.5 to -1.9) to -2.9 (-5.4 to -0.5) over 2.7 (1.0-6.0) years and was -3.0 (-6.3 to -0.1) at final height (NS). In group 3 Ht SDS increased from -3.4 (-4.3 to -2.6) to -3.0 (-3.4 to -2.2) over 1.4 (0.2-2.3) years (NS) and was -2.5 (-3.0 to -1.9) at final height (P=0.03 from stopping rhGH to final height). Final height was attained in 13 patients, in whom Ht SDS increased from -3.2 (-4.3 to -1.9) to -2.6 (-3.9 to -0.5) on rhGH (P=0.004) and to -2.2 (-4.4 to -0.1) after stopping treatment (P=0.04). Four patients died, 2 have chronic hepatitis C, and 1 has had surgery for parathyroid adenomata. In conclusion, the majority of patients had an improvement in Ht SDS while on rhGH, which was maintained after stopping treatment.
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