Sleep Intervention Protocols for AuDHD Adults
Companion note to Poor Sleep and AuDHD-HFE Interactions, which establishes why sleep is a central hub in Anthony's case. This note compiles the evidence for specific interventions, with PMIDs, key findings, and evidence ratings.
Evidence Rating Key
- A = Systematic review/meta-analysis or multiple high-quality RCTs
- B = Single well-designed RCT or multiple controlled studies
- C = Pilot study, open-label trial, or strong observational evidence
- D = Expert opinion, case series, or extrapolation from adjacent populations
flowchart TD
subgraph P1["Phase 1 - Foundation - Weeks 1-2"]
HYGIENE["Sleep Hygiene"]
SENSORY["Sensory Environment"]
WAKE["Fixed Wake Time"]
end
GATE1{"ISI Score + Sleep Diary"}
subgraph P2["Phase 2 - Chronobiology - Weeks 2-4"]
MEL["Melatonin - IR + PR"]
CHRONO["Chronotherapy"]
MG["Magnesium - Evening"]
end
GATE2{"DLMO Shift + Sleep Latency"}
subgraph P3["Phase 3 - Behavioural - Weeks 4-8"]
ACT["Adapted CBT-I or ACT-i"]
LIGHT["Morning Bright Light"]
end
GATE3{"ISI + Actigraphy + Function"}
subgraph P4["Phase 4 - Medication Timing - Week 8+"]
ELVANSE["Elvanse Timing Shift"]
REVIEW["Prescriber Review"]
end
HYGIENE --> SENSORY --> WAKE
WAKE --> GATE1
GATE1 -->|"Still impaired"| MEL
MEL --> CHRONO --> MG
MG --> GATE2
GATE2 -->|"Still impaired"| ACT
ACT --> LIGHT
LIGHT --> GATE3
GATE3 -->|"Still impaired"| ELVANSE
ELVANSE --> REVIEW
classDef phase fill:#85c1e9,stroke:#2471a3,color:#0a1929
classDef gate fill:#d5dbdb,stroke:#7f8c8d,color:#1a1a1a
class HYGIENE,SENSORY,WAKE,MEL,CHRONO,MG,ACT,LIGHT,ELVANSE,REVIEW phase
class GATE1,GATE2,GATE3 gate
1. Melatonin
| Citation |
Key Finding |
Rating |
| Palagini L et al. "International Expert Opinions and Recommendations on the Use of Melatonin in the Treatment of Insomnia and Circadian Sleep Disturbances in Adult Neuropsychiatric Disorders." Front Psychiatry 2021. PMID: 34177671 |
PR melatonin 2-10 mg, 1-2h before bedtime, recommended for insomnia in adults with ASD, ADHD, mood disorders, and schizophrenia. IR melatonin at sub-milligram doses (<1 mg) recommended specifically for circadian phase-shifting. |
B |
| Geoffroy PA et al. "The use of melatonin in adult psychiatric disorders: Expert recommendations by the French institute of medical research on sleep (SFRMS)." Encephale 2019. PMID: 31248601 |
French expert consensus: melatonin useful in stabilised ADHD as adjuvant for insomnia and delayed sleep phase. Even at small chronobiotic doses (0.125 mg), melatonin synchronises circadian rhythm; soporific effect increases dose-dependently. |
B |
| Givler D et al. "Chronic Administration of Melatonin: Physiological and Clinical Considerations." Neurol Int 2023. PMID: 36976674 |
Long-term melatonin at low-moderate doses (up to 5-6 mg) appears safe. Sleep-onset effect is modest for most people; sleep-maintenance effect is stronger with sustained-release preparations. Benefits established for ASD populations. |
B |
Melatonin in ASD/ADHD — Key Trials
| Citation |
Key Finding |
Rating |
| Gringras P et al. "Efficacy and Safety of Pediatric Prolonged-Release Melatonin for Insomnia in Children With Autism Spectrum Disorder." J Am Acad Child Adolesc Psychiatry 2017. PMID: 29096777 |
PR melatonin (2-5 mg) increased total sleep time by 57.5 min vs 9.1 min placebo (p=.034), reduced sleep latency by 39.6 min (p=.011) in ASD with/without ADHD. NNT = 3.38. |
A |
| Maras A et al. "Long-Term Efficacy and Safety of Pediatric Prolonged-Release Melatonin for Insomnia in Children with Autism Spectrum Disorder." J Child Adolesc Psychopharmacol 2018. PMID: 30132686 |
52-week follow-up: PR melatonin (2/5/10 mg) maintained +62 min total sleep time, -48.6 min sleep latency, -0.41 nightly awakenings vs baseline. 76% of completers achieved clinically meaningful improvement. No tolerance, no withdrawal effects. Caregiver QoL also improved. |
A |
| Malow BA et al. "Sleep, Growth, and Puberty After 2 Years of Prolonged-Release Melatonin in Children With Autism Spectrum Disorder." J Am Acad Child Adolesc Psychiatry 2021. PMID: 31982581 |
104-week follow-up: PR melatonin remained effective with no evidence of tolerance or safety concerns (fatigue 6.3%, somnolence 6.3% most common adverse events). |
A |
| Parvataneni T et al. "Perspective on Melatonin Use for Sleep Problems in Autism and Attention-Deficit Hyperactivity Disorder: A Systematic Review of Randomized Clinical Trials." Cureus 2020. PMID: 32617211 |
Systematic review of 6 RCTs: melatonin 2-10 mg significantly improved sleep duration and sleep latency vs placebo across ASD and ADHD. Well tolerated and safe. |
A |
| Paditz E et al. "The Pharmacokinetics, Dosage, Preparation Forms, and Efficacy of Orally Administered Melatonin for Non-Organic Sleep Disorders in ASD." Children (Basel) 2025. PMID: 40426828 |
Systematic review of 5 RCTs in ASD: recommends starting with low-dose, non-delayed (IR) preparations for rapid onset. Pharmacokinetic data suggests individual melatonin metabolism varies widely in ASD — start low, titrate up. |
A |
Melatonin in ADHD Adults with DSPS — Direct Evidence
| Citation |
Key Finding |
Rating |
| van Andel E et al. "Effects of chronotherapy on circadian rhythm and ADHD symptoms in adults with ADHD and DSPS: a randomized clinical trial." Chronobiol Int 2021. PMID: 33121289 |
RCT (n=51 adults with ADHD+DSPS): 0.5 mg/day melatonin advanced DLMO by 1h28 (p=.001) and reduced ADHD symptoms by 14% (p=.038). Effects reversed 2 weeks after cessation, confirming ongoing treatment needed. |
B |
1.2 Practical Recommendations for Anthony
- Circadian shifting: IR melatonin 0.5 mg, timed 3h before current dim-light melatonin onset (likely ~20:30-21:00 given AuDHD evening chronotype)
- Sleep-onset and maintenance: PR melatonin 2 mg at bedtime, titrate to 5 mg if needed
- Can combine both: low-dose IR for circadian shift + PR for sleep maintenance (per Palagini et al.)
- No tolerance seen in up to 2-year follow-up studies
- Iron interaction note: melatonin has antioxidant properties and may offer some ferroptosis protection — a secondary benefit given HFE status (see Ferroptosis and Neuronal Iron)
2. CBT-I Adapted for Neurodivergent Adults
2.1 Why Standard CBT-I May Fail in AuDHD
Standard CBT-I relies on:
- Sleep restriction — difficult when ADHD executive dysfunction prevents schedule adherence
- Stimulus control (leave bed if awake >20 min) — problematic for autistic adults with transition difficulties and sensory need for familiar environment
- Cognitive restructuring — may miss the point when insomnia is driven by sensory overload or circadian biology rather than maladaptive cognitions
- Homework compliance — executive function demands are high
2.2 Evidence for Adapted Approaches
| Citation |
Key Finding |
Rating |
| Cullen M et al. "Effectiveness of Cognitive Behavioural Therapy for Insomnia (CBT-I) in Individuals With Neurodevelopmental Conditions: A Systematic Review." J Sleep Res 2025. PMID: 40180888 |
Systematic review of 8 studies (n=598, ASD and/or ADHD): CBT-I showed significant short-term effectiveness but improvements were mostly not maintained at follow-up. Quality was moderate. Key gap: no consensus on how to adapt CBT-I for neurodevelopmental populations. |
B |
| Jernelov S et al. "Effects and clinical feasibility of a behavioral treatment for sleep problems in adult ADHD." BMC Psychiatry 2019. PMID: 31340804 |
Pilot study (n=19 ADHD adults): 10-week group CBT-i adapted for ADHD reduced ISI by 4.5 points at post-treatment, 6.8 points at 3-month follow-up (both p<.01). 79% were on stimulant medication. Shows CBT-i is feasible and effective in medicated ADHD adults. |
C |
| Lawson LP et al. "ACT-i, an insomnia intervention for autistic adults: a pilot study." Behav Cogn Psychother 2023. PMID: 36537291 |
Pilot (n=8 autistic adults): Acceptance and Commitment Therapy for insomnia (ACT-i) significantly improved ISI (p=.006) and anxiety (p=.015). 5/8 showed clinically reliable improvement. Rated highly acceptable by participants. ACT's emphasis on psychological flexibility rather than thought challenging may be better suited to autism. |
C |
| Kragh M et al. "Efficacy of a Transdiagnostic Sleep and Circadian Intervention for Outpatients With Sleep Problems and Depression, ADHD, or Bipolar Disorder: A Randomised Controlled Trial." J Sleep Res 2026. PMID: 40345174 |
RCT (n=88, including ADHD): transdiagnostic intervention combining CBT-I with chronotherapy significantly improved sleep quality (p<.001), reduced insomnia severity (p<.001), and improved well-being, recovery, and work ability vs sleep hygiene alone. 6 individual sessions. |
B |
| Spaargaren KL et al. "Protocol of a randomized controlled trial into guided internet-delivered CBT-I for insomnia in autistic adults (i-Sleep Autism)." Contemp Clin Trials 2024. PMID: 39357740 |
RCT protocol (n=160 planned): co-created with autistic adults, adapting existing i-Sleep intervention. Includes sensory and information processing accommodations. Trial ongoing — watch for results. |
D (protocol only) |
| Bijlenga D et al. "The role of the circadian system in the etiology and pathophysiology of ADHD: time to redefine ADHD?" Atten Defic Hyperact Disord 2019. PMID: 30927228 |
Review establishing DSPS prevalence at 73-78% in ADHD. Argues that a substantial ADHD subgroup has chronic sleep disorders as root cause of symptoms. Recommends chronotherapy + sleep hygiene + specific sleep disorder treatment before or alongside ADHD medication. |
B |
2.3 Key Adaptations for AuDHD CBT-I
Based on the above evidence:
- Replace rigid sleep restriction with gradual sleep window compression — less executive demand
- Use ACT-based approaches (acceptance, defusion) instead of pure cognitive restructuring — suits autistic thinking styles
- Combine with chronotherapy (light, melatonin, fixed wake time) — targets the ADHD circadian biology
- Build in external structure (alarms, apps, visual schedules) — accommodates ADHD executive dysfunction
- Address sensory environment explicitly — not a standard CBT-I component but essential for autism
- Internet-delivered formats may suit autistic adults who prefer reduced social demand
3. Chronotherapy
3.1 Evidence for Morning Bright Light + Fixed Wake Times in ADHD
| Citation |
Key Finding |
Rating |
| van Andel E et al. "Effects of chronotherapy on circadian rhythm and ADHD symptoms in adults with ADHD and DSPS." Chronobiol Int 2021. PMID: 33121289 |
RCT (n=51): melatonin 0.5 mg advanced DLMO by 1h28; melatonin + 30-min morning bright light (10,000 lux, 07:00-08:00) advanced DLMO by 1h58 (p<.001). However, melatonin alone reduced ADHD symptoms while the combination did not — possibly because early morning light was burdensome and reduced compliance. |
B |
| van Andel E et al. "ADHD and Delayed Sleep Phase Syndrome in Adults: A Randomized Clinical Trial on the Effects of Chronotherapy on Sleep." J Biol Rhythms 2022. PMID: 36181304 |
Secondary analysis of the same RCT: despite DLMO advancing, actual sleep times did not advance to match. Conclusion: chronotherapy shifts the clock but extensive behavioral coaching is needed to shift behavior along with it. |
B |
| van Andel E et al. "Effects of Chronotherapeutic Interventions in Adults With ADHD and DSPS on Regulation of Appetite and Glucose Metabolism." J Atten Disord 2024. PMID: 39318134 |
Exploratory: melatonin treatment altered appetite-regulating hormones (decreased leptin and insulin), suggesting chronotherapy may affect metabolic regulation beyond sleep. |
C |
| Bijlenga D et al. "The role of the circadian system in ADHD." Atten Defic Hyperact Disord 2019. PMID: 30927228 |
Review: 73-78% of ADHD adults have delayed circadian rhythm. Proposes chronotherapy (bright light, melatonin, fixed wake time) as adjunctive ADHD treatment. Recommends phase-advancing protocol as standard of care. |
B |
3.2 Practical Protocol for Anthony
Based on the van Andel trial results:
- Low-dose melatonin (0.5 mg) timed 3h before current DLMO, advancing weekly by 1h
- Morning bright light (10,000 lux, 30 min) — but must be paired with behavioral structure
- Fixed wake time 7 days/week — the single most important anchor
- Critical insight: the clock can advance without behaviour following — needs external structure (alarm, accountability, morning routine reward)
- Consider a dawn simulator as lower-demand alternative to light box for the autism sensory profile
4. Sensory Environment Interventions
4.1 Weighted Blankets
| Citation |
Key Finding |
Rating |
| Ekholm B et al. "A randomized controlled study of weighted chain blankets for insomnia in psychiatric disorders." J Clin Sleep Med 2020. PMID: 32536366 |
RCT (n=120, MDD/BD/GAD/ADHD): weighted chain blanket significantly reduced ISI vs light blanket (Cohen's d = 1.90, large effect). Improved sleep maintenance, daytime activity, reduced fatigue/depression/anxiety. Effects maintained at 12-month open follow-up. Included ADHD patients. |
B |
| Yu J et al. "Effect of weighted blankets on sleep quality among adults with insomnia: a pilot randomized controlled trial." BMC Psychiatry 2024. PMID: 39501163 |
Pilot RCT (n=102): weighted blanket group showed significantly greater PSQI improvement (-4.1 vs -2.0, p=.006), plus reduced anxiety, stress, fatigue, and pain. Actigraphy showed trend toward fewer awakenings. |
B |
| Wong S et al. "The effect of weighted blankets on sleep quality and mental health symptoms in people with psychiatric disorders: A systematic review and meta-analysis." J Psychiatr Res 2024. PMID: 39341068 |
SR/MA (9 studies, n=553, psychiatric populations including ADHD and autism): weighted blankets significantly reduced anxiety (SMD=-0.47, p<.001). Mixed evidence for insomnia specifically but trend toward benefit. |
B |
| Zhao Y et al. "Safety and effectiveness of weighted blankets for symptom management in patients with mental disorders." Complement Ther Med 2024. PMID: 39447684 |
SR/MA (8 RCTs, n=426): small-magnitude decrease in anxiety (SMD=0.40). Sensitivity analysis of homogeneous studies showed significant ISI reduction (MD=-2.78, p=.001). No serious adverse events. |
B |
4.2 Sensory Processing and Sleep in Autism
| Citation |
Key Finding |
Rating |
| Lane SJ et al. "Sleep, Sensory Integration/Processing, and Autism: A Scoping Review." Front Psychol 2022. PMID: 35656493 |
Scoping review (24 studies): co-existence of sleep concerns and sensory integration/processing differences is frequently reported in autism. Both hyper- and hypo-reactivity linked to sleep disruption. Pressure-based and movement-based interventions show promise but lack rigorous study. |
C |
| Goldman SE et al. "Characterizing Sleep in Adolescents and Adults with Autism Spectrum Disorders." J Autism Dev Disord 2017. PMID: 28286917 |
ASD adolescents/adults (n=28 vs 13 TD): longer sleep latencies, more difficulty going to bed and falling asleep. Insomnia is multifactorial — not solely physiological (melatonin). Poor sleep hygiene present in both groups. |
C |
4.3 Practical Sensory Protocol for Anthony
Based on the evidence and the autism sensory profile:
- Weighted blanket (8-12 kg): strong evidence for insomnia in psychiatric populations including ADHD; the deep pressure input addresses proprioceptive seeking common in autism
- Complete blackout: eliminate all light sources (particularly blue/green wavelengths) — addresses visual hyper-reactivity
- Consistent sound masking (white/pink noise or brown noise): blocks auditory triggers; no specific ASD RCT but mechanistic rationale is strong given auditory hyper-reactivity
- Temperature control: cool room (16-18°C) — sensory overheating is a common autistic sleep disruptor
- Consistent tactile environment: same bedding texture, avoid changes — supports routine and reduces sensory surprises
5. Stimulant Timing Optimisation (Elvanse / Lisdexamfetamine)
5.1 Available Evidence
| Citation |
Key Finding |
Rating |
| Giblin JM & Strobel AL. "Effect of lisdexamfetamine dimesylate on sleep in children with ADHD." J Atten Disord 2011. PMID: 20574056 |
Pilot RCT (n=24 children): LDX did not significantly increase latency to persistent sleep vs placebo on PSG. No significant objective sleep disturbance. However, small sample; authors urge caution in generalising. |
C |
| Wynchank D et al. "Adult ADHD and Insomnia: an Update of the Literature." Curr Psychiatry Rep 2017. PMID: 29086065 |
Review: stimulants can both improve and worsen sleep. In some ADHD adults, stimulants reduce hyperarousal-driven insomnia; in others, they delay sleep onset. Individual variation is high. Late-day residual effects relevant for long-acting formulations. |
B |
| Kooij JJS et al. "Updated European Consensus Statement on diagnosis and treatment of adult ADHD." Eur Psychiatry 2019. DOI: 10.1016/j.eurpsy.2018.11.001 |
European consensus: recommends addressing sleep as part of ADHD treatment. Earlier dosing of long-acting stimulants can reduce sleep-onset effects. If insomnia persists, consider melatonin as adjunct. |
B |
| Ermer J et al. "Lisdexamfetamine Dimesylate: Prodrug Delivery, Amphetamine Exposure and Duration of Efficacy." Clin Drug Invest 2016. DOI: 10.1007/s40261-015-0354-y |
Pharmacokinetic review: LDX has extended Tmax and lower Cmax vs IR d-amphetamine. Therapeutic action extends 10-14 hours post-dose. At 70 mg, d-amphetamine plasma levels remain significant for ~13-14 hours. |
B |
5.2 Practical Implications for Anthony
At Elvanse 70 mg (highest standard dose):
- Pharmacokinetic duration: 13-14 hours of active d-amphetamine
- If taken at 08:00 → active until ~21:00-22:00
- If taken at 07:00 → active until ~20:00-21:00
- Every 1 hour earlier = 1 hour less evening stimulant exposure
Recommendations:
- Take Elvanse as early as feasible — ideally 06:30-07:00 with breakfast
- This is challenging with ADHD delayed sleep phase — creates a conflict between "take meds early" and "wake up early"
- Resolve by anchoring wake time first (chronotherapy) then shifting meds earlier
- If sleep remains problematic, discuss with prescriber: some clinicians use earlier dosing + low-dose IR short-acting top-up at midday rather than one large long-acting dose
- Monitor: if earlier dosing reduces afternoon/evening coverage, this may affect TTM control (see Trichotillomania and Neurodevelopmental Links)
Note: There is no published RCT directly testing "earlier vs later Elvanse dosing" on sleep outcomes. Evidence is extrapolated from pharmacokinetics and expert consensus. This is a significant evidence gap.
6. Magnesium for Sleep
6.1 General Sleep Evidence
| Citation |
Key Finding |
Rating |
| Hausenblas HA et al. "Magnesium-L-threonate improves sleep quality and daytime functioning in adults with self-reported sleep problems." Sleep Med X 2024. PMID: 39252819 |
RCT (n=80): Mg-L-threonate 1g/day for 21 days significantly improved deep sleep score, REM sleep score, energy, mood, and mental alertness vs placebo. Mg-threonate is notable for brain bioavailability. |
B |
| Schuster J et al. "Magnesium Bisglycinate Supplementation in Healthy Adults Reporting Poor Sleep." Nat Sci Sleep 2025. PMID: 40918053 |
RCT (n=155): Mg bisglycinate 250 mg elemental/day significantly reduced ISI vs placebo at 4 weeks (p=.049). Effect size was small (Cohen's d=0.2). Greater improvement in those with lower baseline dietary Mg. |
B |
| Nielsen FH et al. "Magnesium supplementation improves indicators of low magnesium status and inflammatory stress in adults older than 51 years with poor quality sleep." Magnes Res 2010. PMID: 21199787 |
RCT (n=100): Mg supplementation improved sleep-related inflammatory markers (CRP) in those with low baseline Mg. PSQI improved in both groups (possible placebo effect confounded). Establishes Mg status-sleep quality association. |
C |
6.2 Magnesium in ADHD/Autism Context
| Citation |
Key Finding |
Rating |
| Mousain-Bosc M et al. "Magnesium VitB6 intake reduces central nervous system hyperexcitability in children." J Am Coll Nutr 2004. PMID: 15466962 |
Open study (n=52 hyperexcitable children, 30 with low erythrocyte Mg): Mg + B6 (100 mg/day) for 1-6 months normalised erythrocyte Mg and significantly reduced hyperexcitability symptoms including agitation, attention deficits, and muscle hypertonicity. |
C |
| Arnold LE. "Alternative treatments for adults with ADHD." Ann N Y Acad Sci 2001. PMID: 11462750 |
Review: magnesium supplementation listed among treatments with "promising prospective pilot data" for ADHD. Noted that Mg deficiency is common in ADHD and supplementation may benefit a subgroup with confirmed low status. |
D |
| Cortese S et al. "Sleep Disorders in Children and Adolescents with Autism Spectrum Disorder: Diagnosis, Epidemiology, and Management." CNS Drugs 2020. PMID: 32112261 |
Comprehensive review: identifies melatonin as having the strongest evidence (large effect sizes in meta-analysis of 5 RCTs). Does not provide RCT evidence for magnesium specifically in ASD sleep, reflecting the evidence gap. |
A (for the review; D for Mg in ASD sleep specifically) |
6.3 Practical Recommendations for Anthony
- Best evidence forms for sleep: Mg-L-threonate (brain bioavailability, RCT evidence) or Mg bisglycinate (RCT evidence, good tolerability)
- Dose: 200-400 mg elemental magnesium, taken in the evening
- Rationale beyond sleep: Mg is a cofactor for >300 enzymes including those involved in GABA synthesis, neurotransmitter regulation, and inflammatory modulation — all relevant to AuDHD
- Iron interaction note: Mg and iron compete for absorption; take Mg supplements at a different time of day from any iron-containing foods/supplements
- Evidence gap: no published RCT of magnesium for sleep specifically in ADHD or autism adults — current evidence is extrapolated from general population RCTs and ADHD symptom studies
- HFE relevance: Mg deficiency increases oxidative stress; repletion may offer secondary antioxidant benefit (see Copper-Zinc-Iron Interactions)
7. Integrated Protocol Summary
Based on the totality of evidence reviewed, a staged intervention protocol:
| Intervention |
Action |
Evidence Level |
| Sensory environment |
Weighted blanket, blackout, sound masking, cool room |
B |
| Fixed wake time |
Set consistent alarm 7 days/week, regardless of sleep quality |
B |
| Elvanse timing |
Shift to within 30 min of waking, aim for 06:30-07:00 |
B (extrapolated) |
Phase 2 — Add Melatonin (Week 2-4)
| Intervention |
Action |
Evidence Level |
| IR melatonin |
0.5 mg, 3h before target bedtime, for circadian shift |
B |
| PR melatonin |
2 mg at bedtime, titrate to 5 mg if needed for maintenance |
A |
| Magnesium |
Mg-L-threonate or bisglycinate, 200-400 mg elemental, evening |
B |
Phase 3 — Add Light Therapy (Week 4-6)
| Intervention |
Action |
Evidence Level |
| Morning bright light |
10,000 lux for 20-30 min within 1h of waking |
B |
| OR dawn simulator |
Gradual light increase 30 min before alarm (lower sensory demand) |
D |
Phase 4 — Behavioural (Week 6+)
| Intervention |
Action |
Evidence Level |
| Adapted CBT-I/ACT-i |
ACT-based approach preferred over traditional CBT-I; online delivery may suit |
C |
| Transdiagnostic sleep intervention |
Combines CBT-I + chronotherapy in 6 sessions (Kragh et al. model) |
B |
8. Evidence Gaps and Watch List
- No RCT of melatonin specifically in AuDHD adults — adult evidence is from ADHD+DSPS (van Andel) or extrapolated from paediatric ASD trials
- No RCT of Elvanse timing on sleep — pharmacokinetic reasoning only
- No RCT of magnesium for sleep in ADHD/ASD — extrapolated from general population
- i-Sleep Autism trial (PMID: 39357740) — internet CBT-I co-designed with autistic adults, results pending
- White noise/sound masking in autism — mechanistic rationale strong but no sleep-focused RCT identified
- Iron status and melatonin synthesis: tryptophan hydroxylase is iron-dependent; iron overload could theoretically alter endogenous melatonin production — unstudied intersection relevant to HFE (see Iron and Circadian Rhythm, Tryptophan-Kynurenine Pathway)
Cross-References