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GH Dose Reduction Maintains Normal Prepubertal Height Velocity After Initial Catch-Up Growth in Short Children
Ralph Decker1,2, Kerstin Albertsson-Wikland3, Berit Kriström4
1Gothenburg Pediatric Growth Research Center, Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Insights
Reducing growth hormone (GH) dose by 50% after catch-up growth (CUG) in children maintained height SDS and normal growth velocity. This individualized approach supports effective maintenance treatment during the prepubertal period.
Area of Science:
- Pediatric Endocrinology
- Growth Hormone Therapy
- Child Development
Background:
- Growth hormone (GH) dosing is guided by responsiveness during catch-up growth (CUG).
- Optimal GH dosing strategies for the prepubertal maintenance treatment period remain unclear.
- Individualized GH dosing based on responsiveness is established for CUG.
Purpose of the Study:
- To assess if a 50% reduced individualized GH dose can maintain channel parallel growth (normal height velocity) post-CUG.
- To evaluate the maintenance of standard deviation score (SDS) channel growth after reducing GH dosage.
- To compare outcomes of reduced individualized GH dose with unchanged individualized and standard fixed doses.
Main Methods:
- Prepubertal children (n=98) with CUG were randomized post-treatment.
- Groups received either a 50% reduced individualized dose (GHRID), unchanged individualized dose (GHUID), or standard fixed dose (GHFIX).
- Primary endpoint was the proportion of children maintaining height SDS within ±0.3 at 1 year.
Main Results:
- 85% of the GHRID group maintained height SDS within ±0.3, significantly higher than GHUID (41%) and GHFIX (48%) groups.
- The GHRID group showed significantly improved IGF-1 SDS levels compared to control groups at 3 months and 1 year.
- Channel parallel growth and IGF-1 SDS within ±2 were maintained with the reduced individualized dose.
Conclusions:
- A 50% reduction in individualized GH dose effectively maintains channel parallel growth post-CUG.
- Individualized GH dosing, even at a reduced level, is effective for prepubertal maintenance treatment.
- This strategy supports normal growth velocity and IGF-1 levels in children after CUG.
Context:
GH responsiveness guides GH dosing during the catch-up growth (CUG) period; however, little is known regarding GH dosing during the prepubertal maintenance treatment period.
Objective:
To evaluate whether SD score (SDS) channel parallel growth with normal height velocity can be maintained after CUG by reducing the GH dose by 50% in children receiving doses individualized according to estimated GH responsiveness during the catch-up period.
Design And Settings:
Prepubertal children (n = 98; 72 boys) receiving GH during CUG (GH deficient, n = 33; non-GH deficient, n = 65), were randomized after 2 to 3 years to either a 50% reduced individualized dose (GHRID; n = 27; 20 boys) or unchanged individualized dose (GHUID; n = 38; 27 boys). Another 33 children (25 boys) continued a standard weight-based dose [43 µg/kg/d (GHFIX)].
Main Outcome Measures:
The primary endpoint was the proportion of children with ΔheightSDS within ±0.3 at 1 year after GH dose reduction compared with two control groups: GHUID and GHFIX. The hypothesis was that heightSDS could be maintained within ±0.3 with a reduced individualized GH dose.
Results:
For the intention-to-treat population at 1 year, 85% of the GHRIDgroup maintained ΔheightSDS within ±0.3 vs 41% in the GHUIDgroup (P = 0.0055) and 48% in the GHFIXgroup (P = 0.0047). The ΔIGF-ISDS in the GHRID group was -0.75 ± 1.0 at 3 months (P = 0.003) and -0.72 ± 1.2 at 1 year compared with the GHUID group (0.15 ± 1.2; P = 0.005) and GHFIX group (0.05 ± 1.0; P = 0.02).
Conclusions:
Channel parallel growth (i.e., normal height velocity) and IGF-ISDS levels within ±2 were maintained after completed CUG using a 50% lower individualized dose than that used during the CUG period.
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