Menu
Peptide Database
Results
No peptides found
Featured

Use search to browse all 100+ peptides

Mod GRF 1-29

Sermorelin, Growth Hormone Releasing Hormone (1-29), hGRF(1-29)NH2

Quick Stats
Studies 227
Trials 47
Score 3
1986 pubmed

Testing with growth hormone-releasing factor (GRF(1-29)NH2) and somatomedin C measurements for the evaluation of growth hormone deficiency.

Ranke. M B MB; Gruhler. M M; Rosskamp. R R; Brügmann. G G; Attanasio. A A; Blum. W F WF; Bierich. J R JR

Key Findings

  • GRF‑1‑29 (1 µg/kg IV) produces the same GH response as GRF‑1‑40 in young adults.
  • In children, a peak GH >10 ng/ml after GRF‑1‑29 is a good marker of normal GH function.
  • GH response to GRF‑1‑29 does not depend on age, sex, or puberty in non‑deficient subjects, but declines with age in those with GHD.

Practical Outcomes

  • For biohackers interested in GH‑boosting, GRF‑1‑29 is confirmed as an effective acute secretagogue at a dose of about 1 µg per kg body weight (IV in the study, likely similar subcutaneously). A peak GH >10 ng/ml suggests a normal response, while lower peaks may indicate deficiency. Combining a GRF test with a baseline IGF‑1 (somatomedin C) measurement can give a quick, relatively safe snapshot of GH status before considering longer‑term supplementation.

Summary

The study shows that a single IV dose of growth‑hormone‑releasing factor (GRF‑1‑29) reliably triggers a GH surge in healthy people and can be used to spot growth‑hormone deficiency. A GH level above 10 ng/ml after the test is considered normal, and the shorter GRF‑1‑29 works just as well as the longer GRF‑1‑40.

Abstract

Growth hormone (GH) responses to GRF (1 microgram/kg BW i.v.) were investigated. Comparison between GRF(1-40) and GRF(1-29)NH2 in 11 young adult volunteers gave identical results. One hundred and thirty-one children and adolescents (45 with idiopathic GHD) were tested with GRF (1-29)NH2. The maximal GH levels (max GH) in response to GRF during the 120 min test period were found suitable to characterize the response. In cases without GHD no correlation to age, sex and pubertal development was observed. A maximal GH level of above 10 ng/ml was found to be normal. In 3 out of 86 children without GHD (one with Turner syndrome; two with simple obesity) max GH fell short of 10 ng/ml, while 11 of 45 cases with GHD exceeded this margin. In GHD, max GH was inversely correlated with age. There was no difference in max GH between groups with or without perinatal pathology as a presumed cause of GHD. GH levels to GRF were positively correlated with maximal GH level during sleep in GHD, but not correlated with responses seen to insulin or arginine. The value of GRF testing for the confirmation of GHD is discussed in the light of other GH stimulatory tests and basal somatomedin C measurements. It is suggested that the combination of testing with GRF and the determination of a basal SmC level offers a safe and convenient way to diagnose GHD in clinically suspected cases, though in some cases further diagnostic tests may be needed.

Study Information

Provider

pubmed

Year

1986

DOI

10.1007/bf02429048