Table 3.
Study Design | Country | No. | Age Group | Disease | Daily Dosage (g/d) | Duration | Rating Scale | End Point | |
---|---|---|---|---|---|---|---|---|---|
Nemets et al., 2006 [76] | Randomised controlled trial | Israel | 28 | 6–12 years | - MDD | 400 mg/d EPA and 200 mg/d DHA or placebo | 4 weeks | - CDRS - CDI - CGI |
Highly significant effects of omega-3 on symptoms using the CDRS (p = 0.003), CDI (p < 0.005), and CGI (p = 0.002). |
Young et al., 2017 [78] | Randomised controlled trial | USA | 72 | 7–14 years | - MDD (n = 37) - dysthymic disorder (n = 5) -depressive disorder not otherwise specified (n = 30) |
- 2 g/d n3-PUFAs in monotherapy - PEP in monotherapy- PEP + n3-PUFA - placebo |
12 weeks | - SNAP-IV - ECBI |
N-3 PUFAs yielded more favourable trajectories than placebo on the SNAP-IV Hyperactivity/Impulsivity subscale (p = 0.034, d = 0.44) and marginally more favourable on Total (p = 0.080, d = 0.42), and Inattention scores (p = 0.059, d = 0.49). |
Vesco et al., 2018 [68] | Randomised controlled trial | USA | 95 | 7–14 years | - BP-NOS or CYC (n = 23) - Depressive disorder (n = 72) |
- 1.87 g/d n3-PUFAs in monotherapy - PEP monotherapy - PEP + n3-PUFAs |
12 weeks | - BRIEF - GEC - BRI - YMRS |
PUFAs supplementation were associated with significant improvement in executive functions and in dysphoric mood, irritability, and self-esteem. |
Trebatická et al., 2020 [77] | Randomised, double-blind, placebo controlled trial | Slovakia | 60 | 7–18 years | -MDD (n = 31) -Mixed anxiety and depressive disorder (n = 29) |
2400 mg of total omega-3 PUFAs/day or placebo | 12 weeks | - CDI | PUFAs supplementation were associated with reductions in Children’s Depression Inventory (CDI) scores. |
BRI: Behaviour Regulation; BRIEF: Behaviour Rating Inventory of Executive Functioning; CDI: Child Development Inventory; CDRS: Children’s Depression Rating Scale; CGI Clinical Global Impressions; GEC: Global Executive Composite; ECBI: Eyberg Child Behaviour Inventory; SNAP-IV: Swanson, Nolan, and Pelham-IV.