Literature DB >> 22370992

Effects of large doses of arachidonic acid added to docosahexaenoic acid on social impairment in individuals with autism spectrum disorders: a double-blind, placebo-controlled, randomized trial.

Kunio Yui1, Mamiko Koshiba, Shun Nakamura, Yuji Kobayashi.   

Abstract

Autism spectrum disorders are a neurodevelopmental disorders with reduced cortical functional connectivity relating to social cognition. Polyunsaturated fatty acids arachidonic acid (ARA) and docosahexaenoic acid (DHA) may have key role in brain network maturation. In particularly, ARA is important in signal transduction related to neuronal maturation. Supplementation with larger ARA doses added to DHA may therefore mitigate social impairment. In a 16-week, double-blind, randomized, placebo-controlled trial, we evaluated the efficacy of supplementation with large doses of ARA added to DHA (n = 7) or placebo (n = 6) in 13 participants (mean age, 14.6 [SD, 5.9] years). To examine underlying mechanisms underlying the effect of our supplementation regimen, we examined plasma levels of antioxidants transferrin and superoxide dismutase, which are useful markers of signal transduction. The outcome measures were the Social Responsiveness Scale and the Aberrant Behavior Checklist-Community. Repeated-measures analysis of variance revealed that our supplementation regimen significantly improved Aberrant Behavior Checklist-Community-measured social withdrawal and Social Responsiveness Scale-measured communication. Treatment effect sizes were more favorable for the treatment group compared with the placebo group (communication: treatment groups, 0.87 vs, placebo, 0.44; social withdrawal: treatment groups, 0.88, vs placebo, 0.54). There was a significant difference in the change in plasma transferrin levels and a trend toward a significant difference in the change in plasma superoxide dismutase levels between the 2 groups. This preliminary study suggests that supplementation with larger ARA doses added to DHA improves impaired social interaction in individuals with autism spectrum disorder by up-regulating signal transduction.

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Year:  2012        PMID: 22370992     DOI: 10.1097/JCP.0b013e3182485791

Source DB:  PubMed          Journal:  J Clin Psychopharmacol        ISSN: 0271-0749            Impact factor:   3.153


  26 in total

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2.  Potential serum biomarkers from a metabolomics study of autism.

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4.  Altered Metabolic Characteristics in Plasma of Young Boys with Autism Spectrum Disorder.

Authors:  Lei Wang; Ruixuan Zheng; Ying Xu; Ziyun Zhou; Ping Guan; Yanling Wu; Jian Zhou; Zaohuo Cheng; Lili Zhang
Journal:  J Autism Dev Disord       Date:  2021-11-20

5.  Supplement intervention associated with nutritional deficiencies in autism spectrum disorders: a systematic review.

Authors:  Yong-Jiang Li; Ya-Min Li; Da-Xiong Xiang
Journal:  Eur J Nutr       Date:  2017-09-07       Impact factor: 5.614

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Authors:  Sarah A Brigandi; Hong Shao; Steven Y Qian; Yiping Shen; Bai-Lin Wu; Jing X Kang
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Review 7.  Profiles of urine and blood metabolomics in autism spectrum disorders.

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Journal:  Metab Brain Dis       Date:  2021-08-02       Impact factor: 3.655

8.  Examining associations between anxiety and cortisol in high functioning male children with autism.

Authors:  David M Simon; Blythe A Corbett
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Review 9.  Chemicals, Nutrition, and Autism Spectrum Disorder: A Mini-Review.

Authors:  Takeo Fujiwara; Naho Morisaki; Yukiko Honda; Makiko Sampei; Yukako Tani
Journal:  Front Neurosci       Date:  2016-04-20       Impact factor: 4.677

Review 10.  Eicosanoids Derived From Arachidonic Acid and Their Family Prostaglandins and Cyclooxygenase in Psychiatric Disorders.

Authors:  Kunio Yui; George Imataka; Hiroyuki Nakamura; Naoki Ohara; Yukiko Naito
Journal:  Curr Neuropharmacol       Date:  2015       Impact factor: 7.363

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