Menu
Peptide Database
Results
No peptides found
Featured

Use search to browse all 100+ peptides

GHRP-2

Pralmorelin, Growth Hormone Releasing Peptide-2, KP-102

Quick Stats
Studies 230
Trials 1
Score 2
2007 pubmed

A simple diagnostic test using GH-releasing peptide-2 in adult GH deficiency.

Chihara. Kazuo K; Shimatsu. Akira A; Hizuka. Naomi N; Tanaka. Toshiaki T; Seino. Yoshiki Y; Katofor. Yuzuru Y

Key Findings

  • A 100 ”g IV dose of GHRP‑2 produces a measurable GH peak in all subjects within 60 minutes.
  • Patients with true GH deficiency have a much lower peak (≈1.4 ”g/L) than healthy people (≈85 ”g/L).
  • A cut‑off of 15 ”g/L (or 9 ”g/L with WHO‑standard calibration) reliably identifies GH deficiency, matching the standard ITT threshold.

Practical Outcomes

  • For biohackers, GHRP‑2 could serve as a faster, safer way to check GH reserve compared to the insulin tolerance test, but it still requires medical‑grade labs and IV administration. The test’s results are modestly affected by age and body fat, so personal baseline values are important. It’s mainly a diagnostic tool, not a performance‑enhancing protocol.

Summary

Researchers showed that giving a single IV dose of GHRP‑2 makes growth hormone spike within an hour, and the size of that spike can tell whether someone has adult growth‑hormone deficiency. A peak GH level below about 15 ”g/L after the test matches the traditional, riskier insulin tolerance test for diagnosing deficiency.

Abstract

The international, first-line diagnostic test for adult GH deficiency is the insulin tolerance test (ITT), which is contraindicated in some patients due to severe adverse events. Alternatives such as GH-releasing hormone combined with arginine or GH-releasing peptides (GHRP) have been proposed. We validated the use of GHRP-2 for diagnosing adult GH deficiency (GHD). Seventy-seven healthy subjects and 58 patients with peak GH<3 microg/l by ITT were enrolled. After overnight fasting, a 100 microg dose of GHRP-2 was administered intravenously; blood samples were taken during the subsequent 2 h and GH measured by immunoradiometric assay. Serum GH peak occurred within 60 min after GHRP-2 administration in all subjects. GH responses to GHRP-2 were not affected by gender, but were slightly lower in elderly subjects and those with adiposity, although these did not influence diagnosis of GHD. Repeated tests showed favourable reproducibility. Peak GH concentrations after GHRP-2 were significantly (P<0.001) lower in patients (1.36+/-2.60 microg/l) than the healthy group (84.6+/-60.9 microg/l) with no difference between hypothalamic and pituitary diseases. Serum GH concentration at the point where sensitivity of response crossed with specificity ranged from 15 to 20 microg/l. A cut-off value of 15 microg/l for diagnosing GHD with GHRP-2 corresponded to the diagnostic value of 3 microg/l in the ITT. The GHRP-2 provocative test showed favourable reproducibility and was mildly influenced by age and adiposity. Severe GH deficiency could be diagnosed with high reliability using a 15 microg/l (9 microg/l when GH calibrated with recombinant World Health Organization 98/574 standard) cut-off for peak GH concentration.

Study Information

Provider

pubmed

Year

2007

DOI

10.1530/eje-07-0066