Bloch · Journal of the American Academy of Child and Adolescent Psychiatry 2011 · systematic review and meta-analysis · n=10 trials (699 children)

Omega-3 fatty acid supplementation for the treatment of children with attention-deficit/hyperactivity disorder symptomatology: systematic review and meta-analysis.

Cited 414 times in the scientific literature.

Level 1 - systematic review of randomized trials

Systematic review and meta-analysis of randomized placebo-controlled trials

PubMed 21961774 · doi:10.1016/j.jaac.2011.06.008 · record verified 2026-08-29

What was done

Authors searched PubMed for randomized placebo-controlled trials evaluating omega-3 fatty acid supplementation in children with attention-deficit/hyperactivity disorder (ADHD) symptomatology. The primary outcome was the standardized mean difference on ADHD severity rating scales. Secondary analyses assessed the relationship between specific omega-3 fatty acid dosages (notably eicosapentaenoic acid, EPA) and clinical efficacy.

What was found

Ten trials comprising 699 children met inclusion criteria. Omega-3 fatty acid supplementation produced a statistically significant, small improvement in ADHD symptoms. Higher doses of EPA within supplements were significantly correlated with greater symptom reduction. The abstract reported no evidence of trial heterogeneity or publication bias; specific numerical effect sizes and confidence intervals were not provided in the abstract.

Why it matters

While omega-3 fatty acid efficacy is modest compared to standard ADHD medications like psychostimulants or atomoxetine, its favorable side-effect profile makes it a viable candidate for augmenting traditional pharmacotherapy or as an option for families who decline psychiatric medications.

Limits

The total sample size across 10 trials is relatively modest (699 participants). The search was limited to PubMed. The abstract does not provide exact effect sizes, confidence intervals, or p-values, nor does it detail treatment durations, background medication status, or specific adverse event rates.

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