Assessment of the Efficacy of Quercetin in Adult Patients With Autism Spectrum Disorder: A Randomized, Triple-Blind, Placebo-Controlled Trial.
- 2026-07
- Human psychopharmacology 41(4)
- Anahid Rezaeifar
- Mahtab Motamed
- Niayesh Mohebbi
- PubMed: 42438230
- DOI: 10.1002/hup.70057
Study Design
- Type
- Randomized Controlled Trial (RCT)
- Population
- 52 adults with autism spectrum disorder (ASD)
- Methods
- randomized, triple-blind, placebo-controlled clinical trial, quercetin or placebo for 60 days
- Blinding
- Triple-blind
- Duration
- 60 days
- Funding
- Unclear
Objectives
This randomized, triple-blind, placebo-controlled clinical trial evaluated the efficacy and safety of quercetin in adults with autism spectrum disorder (ASD).Methods
Fifty-two adults with ASD were randomly assigned to receive either quercetin or placebo for 60 days. Outcomes included the Social Responsiveness Scale (SRS), WHO Quality of Life (WHOQOL) domains, and other clinical measures assessed at baseline, 30 days, and 60 days.Results
Baseline demographic characteristics and comorbid conditions were comparable between groups. The quercetin group showed a significant within-group reduction in SRS scores over time (p = 0.010), whereas the placebo group showed no significant change (p = 0.655). However, between-group differences in SRS change were not statistically significant. At week 8, the physical health domain of WHOQOL improved more in the quercetin group at the unadjusted level (p = 0.044), but this was not significant after adjustment (p = 0.082). The environmental health domain showed a borderline difference favoring quercetin (adjusted p = 0.053).Conclusion
Quercetin supplementation showed potential benefits in select social quality of life and social domain responsiveness in participants with ASD. Larger, well-designed trials are needed to confirm its clinical effectiveness.Trial registration
IRCT20241214064050N1.Research Insights
The environmental health domain showed a borderline difference favoring quercetin (adjusted p = 0.053).
- Effect
- Neutral
- Effect size
- Small
At week 8, the physical health domain of WHOQOL improved more in the quercetin group at the unadjusted level (p = 0.044), but this was not significant after adjustment (p = 0.082).
- Effect
- Neutral
- Effect size
- Small
The quercetin group showed a significant within-group reduction in SRS scores over time (p = 0.010), whereas the placebo group showed no significant change (p = 0.655). However, between-group differences in SRS change were not statistically significant.
- Effect
- Neutral
- Effect size
- Small
Adverse Events Reported
This randomized, triple-blind, placebo-controlled clinical trial evaluated the efficacy and safety of quercetin in adults with autism spectrum disorder (ASD).
- Finding
- Reported