The Journal of Clinical Endocrinology & Metabolism · 1988 · 41 citations · 24 references
MedicineEndocrinologyPediatricsEndocrine PharmacotherapyPediatric EndocrinologyPediatric TherapeuticsChild GrowthGrowth DisordersGrowth HormoneGrowth Hormone TherapyPediatric GrowthPituitary HormonesDurable Clinical ResponseGrowth VelocityGrowth Velocity AssessmentPretreatmentPulsatile Growth Hormone ReleasePulsatile Growth Hormone SecretionPulsatile Hormone ReleasePulsatile Hormone Secretion
We treated seven GH-deficient children with 3-hourly 1 microgram/kg sc pulses of GHRH-(1-44) for 6 months and 2 micrograms/kg.pulse for another 6 months. Four patients had a serum GH response to iv GHRH before treatment, and an additional patient responded to iv GHRH after 1 month of pulsatile sc GHRH administration. The mean cumulative growth velocity increased from a pretreatment mean of 2.7 +/- 0.2 (+/- SE) to 8.4 +/- 2.5 and 5.4 +/- 0.7 cm/yr after 2 months and 1 yr of treatment, respectively. Low dose pulsatile GHRH therapy was effective in promoting growth in five of seven children, with height gain ranging from 4.4-7.5 cm at the end of 1 yr's therapy. Only one of the two patients who did not respond to GHRH had an improvement in linear growth when they were subsequently treated with synthetic GH. The other patient, a 16.5-yr-old pubertal girl who had both satisfactory GH and somatomedin-C responses during GHRH therapy, did not respond to either GHRH or, later, synthetic GH. The pretreatment serum GH response to iv GHRH, the serum somatomedin-C concentrations, and the peak serum GH response during sc GHRH therapy were not reliable predictors of clinical response.
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Growth hormone neurosecretory dysfunction. A treatable cause of short stature
Bessie E. Spiliotis · JAMA · 1984 · 404 citations
Medicine, Endocrinology, Pediatrics +17
M. L. Vance, Donald L. Kaiser, William S. Evans et al. · Journal of Clinical Investigation · 1985 · 177 citations · Full text