IGF-1 is the marker people use to tell whether a growth hormone secretagogue is doing anything. It is also the marker most often quoted without the one piece of context it cannot be interpreted without: how old the person is.
Growth hormone is secreted in pulses, mostly at night, and a random GH measurement is close to meaningless as a result. IGF-1 is produced largely by the liver in response to that GH exposure, circulates bound to binding proteins with a much longer half-life, and is therefore stable enough across a day to be measured once and interpreted.
That is the whole reason IGF-1 is the standard proxy: it integrates GH exposure over time instead of sampling a pulse. IGFBP-3, the main binding protein, is sometimes measured alongside it and moves in the same direction.
Established clinical use IGF-1 peaks in adolescence and declines continuously through adult life.1 A value of 200 ng/mL is unremarkable at twenty-five and high at sixty-five. This is not a minor adjustment: published adult reference intervals run roughly 114–400 ng/mL in the 25–39 band and roughly 70–290 ng/mL over 54.1
That is why the registry marks age as context this marker requires rather than as a nicety, and why a raw IGF-1 quoted with no age attached — as they almost always are in forum posts — cannot be interpreted. Many labs report a Z-score or standard deviation score against an age- and sex-adjusted median for exactly this reason, and where you have one it is more informative than the raw number.
Off-label or community practice The generic band in the fact box is a broad adult default. It is a fallback for when your report did not carry an age-adjusted interval, and it is weaker than the one your lab printed, which is built for your age band.
Established clinical use IGF-1 assays have historically disagreed with each other enough to matter. Calibration against the WHO reference standard has been recommended, and assays conforming to that recommendation have been validated against large multicentre cohorts.12 Not every assay in use is calibrated the same way, and studies comparing two modern immunoassays in the same cohort still find differences worth knowing about.2
The practical consequence is the same as for every other marker on this site: a trend across two laboratories is partly a comparison of two assays. Stay with one lab if you are watching a number move.
What drives it: MK-677, GHRP-2/6, ipamorelin, CJC — water retention and blood-sugar drift come with the territory.
What people report: Tingling hands or carpal-tunnel feeling, puffiness, vivid dreams, raging hunger (GHRP-6 and MK-677 especially).
What to measure: Fasting glucose and HbA1c on anything run for months — GH antagonizes insulin.
Worth knowing: Rising fasting glucose on a GH secretagogue is the signal to cut the dose or stop — insulin resistance is the long-term cost nobody logs.
Anything here is a reason to talk to the clinician who prescribes for you, with the result and the assay in front of you — not a reason to change a protocol on your own.
Off-label or community practice Growth hormone secretagogues — the GHRH analogues like sermorelin, CJC-1295 and tesamorelin, and the ghrelin-receptor agonists like ipamorelin and MK-677 — raise IGF-1 by increasing endogenous GH release rather than by supplying GH. IGF-1 is therefore the reasonable marker for whether one is doing anything measurable, and a rise is the expected finding. Most of these are research compounds with no approval for this use.
The number worth watching alongside it is fasting glucose, and the reason is mechanistic rather than theoretical: growth hormone antagonises insulin. A rising IGF-1 with a drifting fasting glucose is the trade, and the app's own guidance is that a rising fasting glucose on a secretagogue is the signal to reconsider the dose. The HbA1c and fasting glucose page covers what to watch and how often.
How high is too high is not a question with a clean published answer for people using these compounds off-label, because the trials that would establish it have not been done. What is documented is what sustained GH excess does over years in acromegaly, which is the reason the ceiling is worth taking seriously rather than treating a high-normal IGF-1 as a target. That is a discussion for a doctor, with an age-adjusted result in front of you.
Generated by matching this marker's own aliases against the monitoring note on every compound in the app's reference, so the list is the app's, not an author's.
This page will not give you a target, because one does not exist for off-label use. The honest position is that the reference interval for your age says what is ordinary, a Z-score says how far from the age-adjusted median you are, and no trial has established an optimal value for someone taking a secretagogue for body composition or recovery. Anyone quoting a specific target number is quoting a convention, not a finding.
Not in the way glucose does — its long half-life is what makes it stable. Consistency still helps: same lab, same rough time of day, same relationship to your dosing schedule if you are on something that moves it.
Because the age adjustment is the whole point, and a Z-score expresses it directly: it is roughly how many standard deviations you sit from the median for your age and sex. If your report gives one, prefer it to comparing a raw number against a generic adult band.
Every claim above that is not a definition is either labelled by evidence tier or carries a numbered reference to one of these.
TherapyLog logs this marker with the unit, the reference interval your report printed and the assay method beside it, so a trend cannot silently switch methods on you.
Log your bloodworkThis calculator does the arithmetic you typed and nothing else. It does not know what is actually in your vial, whether the label is accurate, or anything about you. Confirm the vial strength and the diluent volume on your own label before you draw, and take dosing decisions to a qualified provider.