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Published on: November 14, 2013
Growth increments with low dose intermittent growth hormone and fluoxymesterone in first year of therapy in
Insights
A lower dose of human growth hormone (hGH) combined with fluoxymesterone effectively improved growth in children with hypopituitarism. This intermittent regimen offers a cost-effective treatment option without accelerating bone age.
Area of Science:
- Pediatric Endocrinology
- Growth Hormone Therapy
Background:
- Commercial human growth hormone (hGH) availability enables exploring optimized treatment protocols.
- Hypopituitarism in children necessitates effective growth hormone replacement therapy.
Purpose of the Study:
- To evaluate the efficacy of a lower, intermittent dose of hGH in children with hypopituitarism.
- To assess the impact of this regimen on growth velocity and bone age.
Main Methods:
- Thirteen children (ages 4-13) received intramuscular hGH (1 IU daily for 12-36 days/course, 4 courses/year) with oral fluoxymesterone (1-2 mg).
- Total annual hGH dose ranged from 48-112 IU, significantly lower than standard regimens (312 IU/year).
Main Results:
- All 13 children demonstrated improved growth velocity, averaging 6.4 cm ± 1.13 SD.
- The mean bone age advancement was 0.57 years ± 0.14 SEM per chronological year of therapy.
- The low-dose regimen achieved significant growth without excessive bone age advancement.
Conclusions:
- An intermittent, lower-dose hGH regimen is effective for treating growth failure in children with hypopituitarism.
- This approach offers a substantial cost reduction compared to higher-dose therapies.
- The treatment strategy balances growth promotion with controlled bone maturation.
Abstract:
The availability of a commercial preparation of human growth hormone (hGH) prompted a study in children with hypopituitarism to determine the efficacy of a lower dose of hGH. Thirteen children, ages 4 years 3 months to 13 years 7 months, were given hGH concomitant with fluoxymesterone in an intermittent regimen. The hGH was given intramuscularly, 1 IU daily for 12 to 36 days in each course. There were four courses per year. The fluoxymesterone was given orally, 1 to 2 mg. The total amount of hGH administered was between 48 and 112 IU per year, as compared with the regimen of 312 IU per year, 2 units three times a week. The growth velocity in all 13 children improved, and the mean growth velocity was 6.4 cm +/- 1.13 SD. The mean bone age increment was 0.57 years +/- 0.14 SEM in one chronological year of therapy. The low dose regimen permits a significant reduction in cost of hGH without causing undue advance in bone age.
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