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. 2021 Jul 21;9(8):850. doi: 10.3390/biomedicines9080850

Table 4.

Anxiety disorder.

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.