The most abundant steroid in circulation, sold over the counter, and genuinely difficult to reason about — because what it becomes depends on the person taking it.
Established clinical use DHEA is an adrenal steroid that sits upstream of both the androgen and the oestrogen pathways. Peripheral tissues convert it to androstenedione and onward to testosterone, and separately to estrone and estradiol, using enzymes whose expression differs by tissue, by sex and by individual. The consequence is that the same dose in two people produces different downstream hormones in different proportions, and neither of them can predict which without measuring.
It circulates mostly as the sulphated ester, DHEA-S, which is far more abundant and far more stable across the day than DHEA itself. That is why DHEA-S is what gets measured: the unsulphated hormone fluctuates with the adrenal rhythm, the sulphate does not. The app puts DHEA-S first on the monitoring panel for exactly that reason, alongside testosterone and estradiol — because the point is not the precursor level but what it turned into.
Levels fall with age from a peak in the twenties, and that decline is the entire origin of the supplementation idea. A decline is not by itself a deficiency, and this is one of the places where the distinction does real work.
Off-label or community practice Randomised trials in older adults have generally found small or absent effects on body composition, strength and quality of life, with the clearest signals in people who started with genuinely low levels — adrenal insufficiency being the case where replacement has the best support. In women, the topical vaginal preparation has a real approval for a real indication, which is a narrower claim than systemic supplementation.
The honest summary is that DHEA does something measurable to circulating hormones in most people and something clinically meaningful in a minority, and that the minority is identified by measuring rather than by symptoms. Taking it without a baseline DHEA-S is the common pattern and the one least likely to inform anything.
Off-label or community practice In hormone-therapy contexts there is a second consideration. Someone already on testosterone is adding a precursor to a system that is already supplied, and the most likely effect is on estradiol rather than on testosterone — the app’s own interaction data flags exactly that. Adding it and then attributing an estradiol rise to the testosterone dose is a common and avoidable confusion.
DHEA is sold as a dietary supplement in the United States and is a controlled or prescription substance in several other countries, including much of Europe. Supplement status means it has not been reviewed for identity, purity or potency the way a drug is, and independent analyses of over-the-counter DHEA products have repeatedly found content varying substantially from the label. This site names no brand and no testing service.
The effects worth watching are the ones you would predict from a steroid precursor: acne and oily skin, hair thinning in people predisposed to it, and in women, hair growth in an androgenic pattern and voice changes at higher doses. Because it aromatises, gynaecomastia is possible in men. Hormone-sensitive cancer is the situation where this is not a casual supplement decision at all.
All of which is to say it deserves the same treatment as any hormone: a baseline measurement, a reason, and a clinician who knows you are taking it. Anything on the drawbacks list below that you are experiencing belongs in front of them.
pkCurve function.
The vertical axis is relative: the shape carries across people, the absolute
concentration does not. This compound’s half-life is flagged as an estimate in the app, so read the curve as the right shape rather than the right numbers.Try other intervals on the half-life and steady-state calculator, which runs the same function against whatever cadence you type.
Established clinical use Reproduced from the app’s reference so you can see what it holds, not as a recommendation. Which row applies to a particular person, if any, is a clinical decision this page does not make — and rows describing supraphysiological or post-cycle use are filtered out before this table is built, so what you see here is a subset.
| Label | Amount | Route and frequency | Duration recorded |
|---|---|---|---|
| Men | 25-50mg/day | Daily oral with morning meal | Ongoing — based on labs |
| Women | 5-25mg/day | Daily oral | Ongoing — lower doses for women |
| Adrenal Support | 10-25mg/day | Daily AM oral | 3-6 months then reassess |
The panel below is the app’s own monitoring note for DHEA, verbatim. The analytes in it that have a page here are linked; those pages cover what each one measures, which assay produced it and how to read a trend.
From the app’s own entry, and the last item — not without a confirmed deficiency — is the one that makes the rest of the list avoidable.
From the app’s interaction data, filtered so no rule naming a compound this site does not publish appears. Not exhaustive, and not a safety clearance: a combination that is not listed is one nobody has documented here, which is not the same as one that is fine. The combination checker has the rest.
DHEA can convert to both testosterone and estrogen. Adding DHEA to a TRT protocol may raise estrogen further. Monitor E2 closely and do not add DHEA without baseline DHEA-S testing.
What to watch: DHEA-S, Total T, Free T, E2 (sensitive assay), PSA. Recheck 6 weeks after adding DHEA.
DHEA aromatizes to estrogen, potentially undermining the estrogen-lowering effect of anastrozole. If using both, E2 monitoring is especially important to confirm AI is achieving target levels.
What to watch: E2 sensitive assay every 6-8 weeks. Adjust anastrozole dose based on labs only.
Pregnenolone is the upstream precursor to DHEA. Using both ensures the adrenal hormone cascade is supported at multiple levels. Start with lower doses of each to assess conversion patterns before increasing.
What to watch: Pregnenolone, DHEA-S, Total T, E2, Cortisol AM. Downstream hormones shift with both compounds.
7-Keto DHEA provides metabolic benefits without hormonal conversion while DHEA provides precursor hormone support. Together they offer broader adrenal optimization. Monitor downstream hormones from DHEA conversion.
What to watch: DHEA-S, Total T, E2. 7-Keto DHEA itself requires no hormonal monitoring.
DHEA-S. The sulphated ester is more abundant and far more stable across the day; unsulphated DHEA follows the adrenal rhythm and a single value is hard to place. Order the downstream hormones alongside it, because those are what the supplement is really changing.
In some people, modestly. In others most of it goes to oestrogens instead, and which one happens depends on individual enzyme expression. That is the reason to measure testosterone and estradiol rather than assume, particularly in men.
The trial evidence is weakest exactly there. The clearest benefit is in people with genuinely low levels, adrenal insufficiency most of all. A normal DHEA-S is a reason to look elsewhere for the symptom.
No. 7-keto is a metabolite that does not convert to testosterone or oestrogen, which makes it a different proposition entirely — the app records it as its own entry with its own regulatory status.
Named rather than linked. Publisher URLs move, and a citation that resolves to a 404 two years from now is worse than one you can search for by name — every entry below is findable from the title and year alone.
A precursor is only readable through what it becomes. TherapyLog keeps DHEA-S, testosterone and estradiol on one chart.
Save this dose to your log