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"Low-dose" growth hormone therapy during peritoneal dialysis or following renal transplantation
I D Schwartz1, B A Warady, C L Buchanan
1Department of Pediatrics, University of Missouri Kansas City School of Medicine, Children's Mercy Hospital, Kansas City 64108, USA.
Insights
Low-dose growth hormone (GH) therapy in children with end-stage renal disease (ESRD) on automated peritoneal dialysis (APD) or after transplantation (T) showed similar height velocity increases. This treatment maintained height Z-scores but did not result in catch-up growth.
Area of Science:
- Pediatric Nephrology
- Endocrinology
- Growth Hormone Therapy
Background:
- The optimal growth hormone (GH) dosage for children with end-stage renal disease (ESRD) undergoing dialysis or renal transplantation is not well-established.
- Children with ESRD often experience growth failure, necessitating therapeutic interventions.
Purpose of the Study:
- To investigate the efficacy of low-dose GH therapy in promoting growth in pediatric patients with ESRD on automated peritoneal dialysis (APD) or post-renal transplantation (T).
- To compare growth parameters, including height velocity and Z-scores, between APD and T patient groups receiving GH treatment.
Main Methods:
- A cohort of children with ESRD receiving chronic APD (n=6) or following renal transplantation (T, n=9) were administered low-dose GH.
- Growth parameters such as height velocity (HV), bone age, height Z-scores (Z-Ht), and height velocity Z-scores (Z-HV) were assessed at baseline, 6 months, and 12 months.
- Renal function was monitored in the T group, and specific patient subgroups were analyzed to account for confounding factors.
Main Results:
- No significant differences in Z-Ht were observed within or between APD and T groups after 6 or 12 months of GH therapy.
- Height velocity Z-scores (Z-HV) significantly increased at 6 and 12 months in APD patients compared to baseline.
- A significant increase in Z-HV was observed in T patients after 12 months of GH treatment when excluding those with the most impaired renal function.
Conclusions:
- Low-dose GH therapy in children with ESRD on APD or following transplantation leads to comparable increases in height velocity.
- This therapeutic approach helps maintain existing height Z-scores but does not facilitate significant catch-up growth in these pediatric populations.
- Further research may be needed to optimize GH dosing strategies for maximizing growth potential in ESRD patients.
Abstract:
The minimal effective dose of growth hormone (GH) to promote growth in children on dialysis or following renal transplantation remains unsettled. In order to study the issue, "low-dose" GH was administered to children with end-stage renal disease (ESRD) receiving chronic automated peritoneal dialysis (APD, n = 6, 4 males, 2 females) or following renal transplantation (T, n = 9, 8 males, 1 female). No APD patient was GH deficient, while 1 T patient (no. 2) had data consistent with GH deficiency, although he was obese (body mass index = 34 kg/m2). The mean dose of GH after 6 and 12 months of treatment was 0.16 +/- 0.02 and 0.22 +/- 0.07 versus 0.16 +/- 0.03 and 0.27 +/- 0.21 mg/kg per week for APD and T patients, respectively. When analyzing all patients, there were no significant differences before or after 6 and 12 months of GH therapy within or between the two groups, in terms of height velocity, bone age, renal function (in the T group) and height Z-scores (Z-Ht). However, the height velocity Z-score (Z-HV) increased significantly at 6 and 12 months compared with baseline in the APD patients only (P < 0.05). When the 2 T patients with the most impaired renal function were excluded from the analysis, Z-HV also increased significantly in the T patients after 12 months of GH (P < 0.02). We conclude that following "low-dose" GH therapy, children with ESRD treated with APD or T have similar increases in HV, allowing maintenance of Z-Ht but not "catch-up" growth.
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