Sermorelin: a review of its use in the diagnosis and treatment of children with idiopathic growth hormone deficiency.
Prakash. A A; Goa. K L KL
Key Findings
- A single IV dose (1 µg/kg) of sermorelin reliably triggers growth hormone release and can be used to test for deficiency.
- Daily sub‑cutaneous doses (30 µg/kg) modestly increase growth rate in pre‑pubertal children with idiopathic GH deficiency.
- Sermorelin’s growth‑promoting effect is smaller than that of standard recombinant growth hormone (somatropin) and long‑term adult height outcomes are unknown.
Practical Outcomes
- For biohackers, sermorelin shows it can safely stimulate GH release, but the evidence for meaningful growth or performance benefits in adults is limited. The dosing used in children isn’t directly transferable to adults, and it appears less effective than direct GH injections. Use mainly as a diagnostic tool rather than a performance‑enhancing protocol.
Summary
Sermorelin is a lab-made peptide that mimics the hormone that tells the pituitary gland to release growth hormone. In kids with unexplained growth hormone deficiency, a single IV dose can help diagnose the problem, and daily injections can modestly boost growth, though not as much as the standard growth hormone drug. It’s generally safe, causing only mild flushing or injection-site pain.
Abstract
Sermorelin, a 29 amino acid analogue of human growth hormone-releasing hormone (GHRH), is the shortest synthetic peptide with full biological activity of GHRH. Intravenous and subcutaneous sermorelin specifically stimulate growth hormone secretion from the anterior pituitary. Hormone responses to intravenous sermorelin 1 microg/kg bodyweight appear to be a rapid and relatively specific test for the diagnosis of growth hormone deficiency. False positive growth hormone responses are observed in fewer children without growth hormone deficiency after sermorelin than after other provocative tests. Adult data indicate that the combination of intravenous sermorelin and arginine is a more specific test and this merits evaluation in children with growth hormone deficiency. However, normal growth hormone responses to intravenous sermorelin cannot exclude growth hormone deficiency due to a hypothalamic deficit: subnormal growth hormone response to other provocative tests is needed to confirm the presence of disease in these patients. Limited data indicate that once daily subcutaneous sermorelin 30 microg/kg bodyweight given at bedtime is effective in treating some prepubertal children with idiopathic growth hormone deficiency. Significant increases in height velocity were sustained during 12 months' treatment with sermorelin and data in a few children suggest the effect is maintained for 36 months of continued treatment. Sermorelin induced catch-up growth in the majority of growth hormone-deficient children. Slow growing, shorter children with delayed bone and height age appear to have a good response to treatment with sermorelin. The effect of long term treatment with once daily subcutaneous sermorelin 30 microg/kg bodyweight on final adult height is yet to be determined. The effects of the recommended dosage of sermorelin have not been directly compared with those of somatropin. However, increases in height velocity from baseline values with subcutaneous sermorelin 30 microg/kg bodyweight per day, given as continuous infusion or as 3 divided doses, were less than those in children receiving once daily subcutaneous somatropin 30 microg/kg bodyweight. Intravenous single dose and repeated once daily subcutaneous doses of sermorelin are well tolerated. Transient facial flushing and pain at injection site were the most commonly reported adverse events. Sermorelin is a well tolerated analogue of GHRH which is suitable for use as a provocative test of growth hormone deficiency when given as a single intravenous 1 microg/kg bodyweight dose in conjunction with conventional tests. Limited data suggest that once daily subcutaneous sermorelin 30 microg/kg bodyweight is effective in promoting growth in some prepubertal children with idiopathic growth hormone deficiency.
Study Information
pubmed
1999
1999-08-01T00:00:00.000Z
10.2165/00063030-199912020-00007
17
48