Table 4.
Study Design | Country | No. | Age Group | Disease | Daily Dosage (g/d) | Duration | Rating Scale | End Point | |
---|---|---|---|---|---|---|---|---|---|
Hamazaki et al., 2005 [83] | Randomised, double-blind, placebo controlled trial | Japan | 22 | 18–24 years | Healthy subjects | - EPA 400 mg/d + DHA 300 mg/d Or placebo |
8 weeks | EP, NE, dopamine, cortisol and corticotropin concentration | PUFAs supplementation were associated with a decreased activation of the hypothalamic–pituitary–adrenal (HPA) axis. |
Kiecolt-Glaser et al., 2011 [84] | Randomised, double-blind, placebo controlled trial | USA | 68 | 21–29 years | Healthy subjects | EPA 2085 mg/d + DHA 348 mg/d or placebo | 12 weeks | -Beck Anxiety Inventory | PUFAs supplementation were associated with 20% reduction in anxiety symptoms, without significant change in depressive symptoms. |
Manos et al., 2018 [85] | Randomised, double-blind, placebo controlled trial | USA | 24 | 12–21 years | - anxiety disorder and AN | - EPA 2120 mg/d + DHA 600 mg/d or placebo | 12 weeks | - BAIT - CES-D - EAT-26 |
No evidence that omega-3 PUFA benefited anxiety. |
Robinson et al., 2019 [86] | Randomised, double-blind, placebo controlled trial | USA | 50 | 15–40 years | - early psychosis and anxiety | - EPA 740 mg/d and DHA 400 mg/d or placebo | 16 weeks | - BPRS - SANS - CGI - SAFTEE-SI |
Implementation with n-3 PUFAs was found mainly useful on depression-anxiety domain measured with the Brief Psychiatric Rating Scale (BPRS). |
BAIT: Beck Anxiety Inventory-Trait; BPRS: Brief Psychosis Rating Scale; CES-D: Centre for Epidemiologic Studies Depression Scale; CGI Clinical Global Impressions; EAT-26: Eating Attitudes Test; SAFTEE-SI: Systematic Assessment for Treatment Emergent Events Specific Inquiry; SANS: Schedule for Assessment of Negative Symptoms.