TY - JOUR
T1 - Efficacy and Safety of Polyunsaturated Fatty Acids Supplementation in the Treatment of Attention Deficit Hyperactivity Disorder (ADHD) in Children and Adolescents
T2 - A Systematic Review and Meta-Analysis of Clinical Trials
AU - Händel, Mina Nicole
AU - Rohde, Jeanett Friis
AU - Rimestad, Marie Louise
AU - Bandak, Elisabeth
AU - Birkefoss, Kirsten
AU - Tendal, Britta
AU - Lemcke, Sanne
AU - Callesen, Henriette Edemann
PY - 2021/4/8
Y1 - 2021/4/8
N2 - Based on epidemiological and animal studies, the rationale for using polyunsaturated fatty acids (PUFAs) as a treatment for Attention Deficit Hyperactivity Disorder (ADHD) seems promising. Here, the objective was to systematically identify and critically assess the evidence from clinical trials. The primary outcome was ADHD core symptoms. The secondary outcomes were behavioral difficulties, quality of life, and side effects. We performed a systematic search in Medline, Embase, Cinahl, PsycInfo, and the Cochrane Library up to June 2020. The overall certainty of evidence was evaluated using Grades of Recommendation, Assessment, Development, and Evaluation (GRADE). We identified 31 relevant randomized controlled trials including 1755 patients. The results showed no effect on ADHD core symptoms rated by parents (k = 23; SMD: -0.17; 95% CI: -0.32, -0.02) or teachers (k = 10; SMD: -0.06; 95% CI: -0.31, 0.19). There was no effect on behavioral difficulties, rated by parents (k = 7; SMD: -0.02; 95% CI: -0.17, 0.14) or teachers (k = 5; SMD: -0.04; 95% CI: -0.35, 0.26). There was no effect on quality of life (SMD: 0.01; 95% CI: -0.29, 0.31). PUFA did not increase the occurrence of side effects. For now, there seems to be no benefit of PUFA in ADHD treatment; however, the certainty of evidence is questionable, and thus no conclusive guidance can be made. The protocol is registered in PROSPERO ID: CRD42020158453.
AB - Based on epidemiological and animal studies, the rationale for using polyunsaturated fatty acids (PUFAs) as a treatment for Attention Deficit Hyperactivity Disorder (ADHD) seems promising. Here, the objective was to systematically identify and critically assess the evidence from clinical trials. The primary outcome was ADHD core symptoms. The secondary outcomes were behavioral difficulties, quality of life, and side effects. We performed a systematic search in Medline, Embase, Cinahl, PsycInfo, and the Cochrane Library up to June 2020. The overall certainty of evidence was evaluated using Grades of Recommendation, Assessment, Development, and Evaluation (GRADE). We identified 31 relevant randomized controlled trials including 1755 patients. The results showed no effect on ADHD core symptoms rated by parents (k = 23; SMD: -0.17; 95% CI: -0.32, -0.02) or teachers (k = 10; SMD: -0.06; 95% CI: -0.31, 0.19). There was no effect on behavioral difficulties, rated by parents (k = 7; SMD: -0.02; 95% CI: -0.17, 0.14) or teachers (k = 5; SMD: -0.04; 95% CI: -0.35, 0.26). There was no effect on quality of life (SMD: 0.01; 95% CI: -0.29, 0.31). PUFA did not increase the occurrence of side effects. For now, there seems to be no benefit of PUFA in ADHD treatment; however, the certainty of evidence is questionable, and thus no conclusive guidance can be made. The protocol is registered in PROSPERO ID: CRD42020158453.
KW - ADHD
KW - Adolescents
KW - Attention deficit hyperactivity disorder
KW - Children
KW - Fatty acids
KW - Meta-analysis
KW - Omega 3
KW - Polyunsaturated
KW - Systematic review
KW - Humans
KW - Treatment Outcome
KW - Clinical Trials as Topic
KW - Fatty Acids, Unsaturated/adverse effects
KW - Adolescent
KW - Quality of Life
KW - Attention Deficit Disorder with Hyperactivity/drug therapy
KW - Child
KW - Dietary Supplements
UR - http://www.scopus.com/inward/record.url?scp=85103832625&partnerID=8YFLogxK
U2 - 10.3390/nu13041226
DO - 10.3390/nu13041226
M3 - Review
C2 - 33917727
SN - 2072-6643
VL - 13
JO - Nutrients
JF - Nutrients
IS - 4
M1 - 1226
ER -