Melatonin

TL;DR

Melatonin is a pineal hormone that signals “time to sleep” via the suprachiasmatic nucleus — it is a circadian entrainment signal, not a hypnotic. At 0.5–5 mg it reduces sleep-onset latency by ~7–17 min; jet lag benefit is well-established (NNT=2, Cochrane-grade). 0.5 mg is nearly as effective as 5 mg for sleep onset. High-dose anti-aging and GH claims are unsubstantiated at supplement doses. Most commercial products are off-label dose; 26% contain undisclosed serotonin.

Why it matters for Vitals

Melatonin is the most accessible sleep-onset intervention with a clear evidence base. Vitals coaching needs to distinguish:

  • what melatonin actually does (sleep-onset timing) vs. what it doesn’t do (sleep quality amplification, GH boost, anti-aging)
  • physiological replacement (0.5 mg) vs. supraphysiological dosing (3–5 mg+)
  • timing sensitivity — taken too late it can cause phase delay; taken 3h before bedtime it outperforms the common 30-min approach

Product sourcing is a real-world risk: 71% of commercial melatonin fails label within 10%, and 26% contain undisclosed serotonin — relevant for users on SSRIs or with cardiac concerns.

Key facts

ParameterValue
MechanismCircadian signal via SCN; not a direct sedative
Sleep onset (adults, 0.5–5 mg)~7–17 min SOL reduction; modest, consistent
Jet lag (≥5 time zones)NNT=2; Cochrane-grade evidence
Pediatric sleep onset37 min earlier onset, 23 min more sleep
Elderly ≥552 mg PR-melatonin (Circadin®); EU-approved
Sleep architectureNo meaningful change at physiological doses (0.3–1 mg)
Recommended dose0.5–4 mg; 0.5 mg nearly as effective as 5 mg
Optimal timing30 min–3 hours before desired bedtime; 3h before outperforms 30 min
Bioavailability9–33%; T½ ~45 min (immediate-release)
MetabolismCYP1A2 → 6-hydroxymelatonin → 6-sulfatoxymelatonin (inactive)
Long-term safetyNo tolerance, withdrawal, or rebound up to 12 months
High-dose (>10 mg)No greater efficacy; more adverse events; GH/anti-aging claims DEBUNKED

Mechanism summary

Melatonin is synthesized from tryptophan in the pineal gland and released in response to darkness, peaking during the biological night (~02:00–04:00). Its primary role is to signal circadian phase to the SCN, not to directly induce sleep. Sleepiness is a downstream consequence of SCN signaling.

Phase-response curve:

  • Late afternoon/early evening → phase advance (earlier sleep)
  • Bedtime or after sleep onset → minimal phase effect
  • Morning → phase delay (later sleep) — counterproductive

Key distinction from hypnotics: Melatonin does not amplify sleep depth or quality at physiological replacement doses. Z-drugs and melatonin act on fundamentally different pathways.

See Circadian Biology for the broader SCN/peripheral clock system.

What the current evidence suggests

Supported

  • Sleep onset (adults): ~7–17 min SOL reduction at 0.5–5 mg. Effect is modest, heterogeneous by population and insomnia subtype. 4 mg at 3h before bedtime outperforms 2 mg at 30 min (Kaufmann 2024, PMID 38888087).
  • Sleep onset (children/adolescents): 37 min earlier onset, 23 min more sleep; strongest evidence in ADHD/ASD populations.
  • Jet lag (≥5 zones): NNT=2; eastward travel benefits most; dose 0.5–5 mg at destination bedtime.
  • Elderly ≥55, primary insomnia: 2 mg controlled-release (Circadin®) approved in EU/Australia.
  • Low vs. standard dose: 0.5 mg nearly as effective as 5 mg for sleep latency.
  • Long-term safety: No tolerance, withdrawal, or rebound up to 12 months.

Contested / gaps

  • Sleep architecture: High doses (≥5 mg) may increase REM; low doses do not alter N1/N3/REM proportions. Sleep architecture is not meaningfully improved at physiological doses.
  • Shift work sleep: Modest sleep length improvement; no global recovery.
  • HPA axis / cortisol: No suppression in waking young men; population-specific data lacking.
  • Anti-inflammatory: Strong preclinical; clinical trials inconclusive at supplement doses.

Debunked at supplement doses

  • GH boost: Human pharmacological data uses gram doses; clinically irrelevant to supplementation.
  • Anti-aging: No human evidence at supplement doses.

Likely wearable / Vitals relevance

See Melatonin Sleep Biometrics and Melatonin Detection Model for full detail.

Summary: Consumer wearables cannot directly detect melatonin ingestion. Any biometric inference (improved SOL, elevated overnight HRV, reduced resting heart rate) is proxy-only and not individually validated for melatonin. These signals are confounded by baseline variation, device noise, and other behavioral factors.

For coaching: the most defensible wearable signal is sleep-onset latency improvement — and even this is within device error margins for most consumers.

Risks and uncertainty

RiskDetail
Product contamination71% off-label dose; 26% contain undisclosed serotonin
Fluvoxamine interactionSevere — 17-fold AUC increase via CYP1A2 inhibition
PregnancyNot recommended
Seizure disordersContested — some EEG abnormality reports
Diabetes3-month use reduced insulin sensitivity in T2D (PMID 35619221)
AnticoagulantsTheoretical platelet inhibition risk
Morning useCan cause phase delay — actively counterproductive

Contamination guardrail: Recommend USP-verified or third-party tested products only. Liquid/gummy formulations carry higher stability and content variance risk.

Best stack context

Melatonin pairs with:

  • Magnesium Glycinate — complementary sleep-onset pathways; both are mild and physiologically rational at low doses
  • L-Theanine — calming without sedation; can combine with melatonin for sleep-onset stack
  • Sleep Optimization — melatonin is one lever in a broader sleep hygiene protocol
  • Light management — melatonin efficacy depends on dim-light environment; pair with Circadian Biology principles

Not a stack candidate with:

  • High-dose GH secretagogues (GH claim is debunked)
  • Anti-aging stacks (unsubstantiated mechanism)

What stays inside this hub

The following are kept inside this hub rather than split into separate notes:

  • GH mechanism (debunked at supplement doses — not reusable)
  • Anti-inflammatory mechanism (preclinical only, not clinically actionable)
  • Specific drug interaction details (available inline)
  • Product sourcing detail (available inline)

In vault:

Implementation: